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Tytuł :
Absence of CCR2 reduces spontaneous intestinal tumorigenesis in the Apc mouse model.
Autorzy :
Jala VR; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Bodduluri SR; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Ghosh S; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Chheda Z; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Singh R; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Smith ME; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Chilton PM; Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky, USA.
Fleming CJ; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Mathis SP; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Sharma RK; James Graham Brown Cancer Center, Department of Medicine, University of Louisville, Louisville, Kentucky, USA.
Knight R; Center for Microbiome Innovation, University of California San Diego, La Jolla, California, USA.
Yan J; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Haribabu B; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
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Źródło :
International journal of cancer [Int J Cancer] 2021 Jan 26. Date of Electronic Publication: 2021 Jan 26.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Regulation of Intestinal Barrier Function by Microbial Metabolites.
Autorzy :
Ghosh S; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky.
Whitley CS; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky.
Haribabu B; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky.
Jala VR; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky. Electronic address: .
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Źródło :
Cellular and molecular gastroenterology and hepatology [Cell Mol Gastroenterol Hepatol] 2021; Vol. 11 (5), pp. 1463-1482. Date of Electronic Publication: 2021 Feb 18.
Typ publikacji :
Journal Article; Review
Czasopismo naukowe
Tytuł :
The role for the metagenome in the pathogenesis of COVID-19.
Autorzy :
Friedland RP; Department of Neurology, University of Louisville School of Medicine, Louisville, KY 40202, United States. Electronic address: .
Haribabu B; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY 40202, United States.
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Źródło :
EBioMedicine [EBioMedicine] 2020 Nov; Vol. 61, pp. 103019. Date of Electronic Publication: 2020 Oct 07.
Typ publikacji :
Letter; Review
MeSH Terms :
Metagenome*
COVID-19/*etiology
COVID-19/microbiology ; Humans ; Inflammation ; Metagenomics
Recenzja
Tytuł :
Microbial Metabolite Urolithin B Inhibits Recombinant Human Monoamine Oxidase A Enzyme.
Autorzy :
Singh R; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Chandrashekharappa S; Institute for Stem Cell Science and Regenerative Medicine (inStem), University of Agricultural Sciences-Gandhi Krishi Vignan Kendra (UAS-GKVK) Campus, Bellary Road, Bangalore, Karnataka 560065, India.
Vemula PK; Institute for Stem Cell Science and Regenerative Medicine (inStem), University of Agricultural Sciences-Gandhi Krishi Vignan Kendra (UAS-GKVK) Campus, Bellary Road, Bangalore, Karnataka 560065, India.
Haribabu B; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Jala VR; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
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Źródło :
Metabolites [Metabolites] 2020 Jun 19; Vol. 10 (6). Date of Electronic Publication: 2020 Jun 19.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Redundant and Cooperative Roles for Yersinia pestis Yop Effectors in the Inhibition of Human Neutrophil Exocytic Responses Revealed by Gain-of-Function Approach.
Autorzy :
Pulsifer AR; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Vashishta A; Department of Medicine, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Reeves SA; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Wolfe JK; Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Palace SG; Department of Microbiology and Physiology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Proulx MK; Department of Microbiology and Physiology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Goguen J; Department of Microbiology and Physiology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Bodduluri SR; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, Kentucky, USA.; James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Haribabu B; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, Kentucky, USA.; James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Uriarte SM; Department of Medicine, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Lawrenz MB; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, Kentucky, USA .; Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, University of Louisville School of Medicine, Louisville, Kentucky, USA.
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Źródło :
Infection and immunity [Infect Immun] 2020 Feb 20; Vol. 88 (3). Date of Electronic Publication: 2020 Feb 20 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Bacterial Proteins/*metabolism
Host-Pathogen Interactions/*physiology
Neutrophils/*physiology
Virulence Factors/*metabolism
Yersinia pestis/*pathogenicity
Bacterial Proteins/genetics ; Cell Degranulation ; Gain of Function Mutation ; Humans ; Leukotriene B4/metabolism ; Neutrophils/metabolism ; Plague/immunology ; Secretory Vesicles/metabolism ; Type III Secretion Systems/genetics ; Type III Secretion Systems/metabolism ; Virulence Factors/genetics ; Yersinia pestis/genetics ; Yersinia pestis/metabolism
Czasopismo naukowe
Tytuł :
Zinc Oxide Nanowires Exposure Induces a Distinct Inflammatory Response via CCL11-Mediated Eosinophil Recruitment.
Autorzy :
Alghsham RS; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Satpathy SR; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Bodduluri SR; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Hegde B; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Jala VR; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Twal W; Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC, United States.
Burlison JA; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Sunkara M; Department of Chemical Engineering, Conn Center for Renewable Energy, University of Louisville, Louisville, KY, United States.
Haribabu B; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
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Źródło :
Frontiers in immunology [Front Immunol] 2019 Nov 08; Vol. 10, pp. 2604. Date of Electronic Publication: 2019 Nov 08 (Print Publication: 2019).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Chemokine CCL11/*immunology
Eosinophils/*drug effects
Eosinophils/*immunology
Inflammation/*etiology
Nanowires/*adverse effects
Zinc Oxide/*adverse effects
Animals ; Chemokine CCL11/genetics ; Chemokine CCL2/genetics ; Disease Models, Animal ; In Vitro Techniques ; Inflammation/genetics ; Inflammation/immunology ; Inflammation Mediators/metabolism ; Interleukin-6/genetics ; Macrophages/drug effects ; Macrophages/immunology ; Mice ; Mice, Inbred C57BL ; Nanowires/chemistry ; Neutrophils/drug effects ; Neutrophils/immunology ; RAW 264.7 Cells ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Tumor Necrosis Factor-alpha/genetics ; Up-Regulation/drug effects ; Zinc Oxide/chemistry
Czasopismo naukowe
Tytuł :
Co-localization of autophagy-related protein p62 with cancer stem cell marker dclk1 may hamper dclk1's elimination during colon cancer development and progression.
Autorzy :
Roy BC; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Ahmed I; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Ramalingam S; Department of Genetic Engineering, School of Bio-Engineering, SRM Institute of Science and Technology, Kattankulathur, Kanchipuram, Tamil Nadu, India.
Jala V; James Graham Brown Cancer Center and Department of Microbiology and Immunology, University of Louisville, Louisville, KY, USA.
Haribabu B; James Graham Brown Cancer Center and Department of Microbiology and Immunology, University of Louisville, Louisville, KY, USA.
Ramamoorthy P; Department of Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Ashcraft J; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Valentino J; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Anant S; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Sampath V; Division of Neonatology, Children's Mercy Hospital, Kansas City, MO, USA.
Umar S; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
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Źródło :
Oncotarget [Oncotarget] 2019 Mar 22; Vol. 10 (24), pp. 2340-2354. Date of Electronic Publication: 2019 Mar 22 (Print Publication: 2019).
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Enhancement of the gut barrier integrity by a microbial metabolite through the Nrf2 pathway.
Autorzy :
Singh R; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USA.
Chandrashekharappa S; Institute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus, Bangalore, Karnataka, 560065, India.
Bodduluri SR; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USA.
Baby BV; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USA.
Hegde B; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USA.
Kotla NG; Institute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus, Bangalore, Karnataka, 560065, India.
Hiwale AA; Institute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus, Bangalore, Karnataka, 560065, India.
Saiyed T; Centre for Cellular and Molecular Platforms (C-CAMP), GKVK campus, Bangalore, Karnataka, 560065, India.
Patel P; Centre for Cellular and Molecular Platforms (C-CAMP), GKVK campus, Bangalore, Karnataka, 560065, India.
Vijay-Kumar M; Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, 43614, USA.
Langille MGI; Department of Pharmacology, Dalhousie University, Halifax, B3H 4R2, Nova Scotia, Canada.
Douglas GM; Department of Pharmacology, Dalhousie University, Halifax, B3H 4R2, Nova Scotia, Canada.
Cheng X; Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, 43614, USA.
Rouchka EC; Computer Engineering and Computer Science, Kentucky Biomedical Research Infrastructure Network, University of Louisville, Louisville, KY, 40202, USA.
Waigel SJ; Department of Medicine, University of Louisville, Louisville, KY, 40202, USA.
Dryden GW; Department of Medicine, University of Louisville, Louisville, KY, 40202, USA.
Alatassi H; Department of Pathology, University of Louisville, Louisville, KY, 40202, USA.
Zhang HG; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USA.
Haribabu B; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USA.
Vemula PK; Institute for Stem Cell Biology and Regenerative Medicine (inStem), GKVK campus, Bangalore, Karnataka, 560065, India. .
Jala VR; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY, 40202, USA. .
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Źródło :
Nature communications [Nat Commun] 2019 Jan 09; Vol. 10 (1), pp. 89. Date of Electronic Publication: 2019 Jan 09.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Coumarins/*pharmacology
NF-E2-Related Factor 2/*metabolism
Tight Junction Proteins/*metabolism
Animals ; Basic Helix-Loop-Helix Transcription Factors/genetics ; Basic Helix-Loop-Helix Transcription Factors/metabolism ; Caco-2 Cells ; Coumarins/chemistry ; Epithelial Cells/metabolism ; Gene Expression Regulation/drug effects ; HT29 Cells ; Humans ; Intestinal Mucosa/metabolism ; Macrophages ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; NF-E2-Related Factor 2/genetics ; Receptors, Aryl Hydrocarbon/genetics ; Receptors, Aryl Hydrocarbon/metabolism ; Specific Pathogen-Free Organisms ; Tight Junction Proteins/genetics
Czasopismo naukowe
Tytuł :
Plant-Derived Exosomal MicroRNAs Shape the Gut Microbiota.
Autorzy :
Teng Y; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA. Electronic address: .
Ren Y; Department of Breast and Thyroid Surgery, The Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University, Huaian, Jiangsu 223300, China.
Sayed M; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA.
Hu X; Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Lei C; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Kumar A; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Hutchins E; Translational Genomics Research Institute, Phoenix, AZ 85004, USA.
Mu J; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Deng Z; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Luo C; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Sundaram K; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Sriwastva MK; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Zhang L; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Hsieh M; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA.
Reiman R; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA.
Haribabu B; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Yan J; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Jala VR; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Miller DM; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Van Keuren-Jensen K; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA.
Merchant ML; Kidney Disease Program and Clinical Proteomics Center, University of Louisville, Louisville, KY, USA.
McClain CJ; Robley Rex Veterans Affairs Medical Center, Louisville, KY 40206, USA; Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, University of Louisville School of Medicine, Louisville, KY 40202, USA.
Park JW; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA; KBRIN Bioinformatics Core, University of Louisville, Louisville, KY 40202, USA.
Egilmez NK; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Zhang HG; Robley Rex Veterans Affairs Medical Center, Louisville, KY 40206, USA; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA. Electronic address: .
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Źródło :
Cell host & microbe [Cell Host Microbe] 2018 Nov 14; Vol. 24 (5), pp. 637-652.e8. Date of Electronic Publication: 2018 Oct 25.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.
MeSH Terms :
Exosome Multienzyme Ribonuclease Complex/*pharmacology
Gastrointestinal Microbiome/*drug effects
Intestines/*microbiology
Intestines/*physiology
MicroRNAs/*pharmacology
Plants/*chemistry
Animals ; Bacterial Proteins ; Colitis/therapy ; Disease Models, Animal ; Disease Susceptibility ; Female ; Food ; Gastrointestinal Microbiome/genetics ; Germ-Free Life ; Host-Pathogen Interactions ; Immunity, Mucosal ; Indoles/metabolism ; Interleukins/metabolism ; Lactobacillus rhamnosus/drug effects ; Lactobacillus rhamnosus/genetics ; Male ; Mice ; Mice, Inbred C57BL ; RNA, Ribosomal, 16S/genetics ; Receptors, Aryl Hydrocarbon/metabolism ; Serine Endopeptidases ; Tryptophan/metabolism
Czasopismo naukowe
Tytuł :
Inflammasome-Independent Leukotriene B 4 Production Drives Crystalline Silica-Induced Sterile Inflammation.
Autorzy :
Hegde B; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Bodduluri SR; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Satpathy SR; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Alghsham RS; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Jala VR; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Uriarte SM; Department of Medicine, University of Louisville Health Sciences Center, Louisville, KY 40202.
Chung DH; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.
Lawrenz MB; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.
Haribabu B; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202; .; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
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Źródło :
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2018 May 15; Vol. 200 (10), pp. 3556-3567. Date of Electronic Publication: 2018 Apr 02.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Inflammasomes/*metabolism
Inflammation/*chemically induced
Inflammation/*metabolism
Leukotriene B4/*metabolism
Silicon Dioxide/*pharmacology
Animals ; Cell Line ; Humans ; Interleukin-1beta/metabolism ; Macrophages/drug effects ; Macrophages/metabolism ; Mast Cells/drug effects ; Mast Cells/metabolism ; Mice ; Mice, Inbred C57BL ; Mitogen-Activated Protein Kinase 8/metabolism ; NLR Family, Pyrin Domain-Containing 3 Protein/metabolism ; Neutrophils/drug effects ; Neutrophils/metabolism ; Phagosomes/drug effects ; Phagosomes/metabolism ; RAW 264.7 Cells ; Silicosis/metabolism ; rab GTP-Binding Proteins/metabolism ; rab5 GTP-Binding Proteins/metabolism
Czasopismo naukowe
Tytuł :
Mast Cell-Dependent CD8 Mice.
Autorzy :
Bodduluri SR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Mathis S; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Maturu P; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Krishnan E; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Satpathy SR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Chilton PM; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.; Institute for Cellular Therapeutics, University of Louisville Health Sciences Center, Louisville, Kentucky.
Mitchell TC; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.; Institute for Cellular Therapeutics, University of Louisville Health Sciences Center, Louisville, Kentucky.
Lira S; Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Locati M; Humanitas Clinical and Research Center, University of Milan, Milan, Italy.; University of Milan, Milan, Italy.
Mantovani A; Humanitas Clinical and Research Center, University of Milan, Milan, Italy.; Humanitas University, Rozzano, Italy.
Jala VR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky. .; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Haribabu B; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky. .; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
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Źródło :
Cancer immunology research [Cancer Immunol Res] 2018 Mar; Vol. 6 (3), pp. 332-347. Date of Electronic Publication: 2018 Jan 30.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
CD8-Positive T-Lymphocytes/*immunology
Intestinal Neoplasms/*immunology
Mast Cells/*immunology
Adenomatous Polyposis Coli Protein/genetics ; Adenomatous Polyposis Coli Protein/immunology ; Animals ; Female ; Immunologic Surveillance ; Leukotriene B4/immunology ; Male ; Mice, Transgenic ; Receptors, Chemokine/genetics ; Receptors, Chemokine/immunology ; Receptors, Leukotriene B4/genetics ; Receptors, Leukotriene B4/immunology
Czasopismo naukowe
Tytuł :
The yin and yang of leukotriene B 4 mediated inflammation in cancer.
Autorzy :
Jala VR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202, USA; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202, USA.
Bodduluri SR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202, USA; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202, USA.
Satpathy SR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202, USA; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202, USA.
Chheda Z; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202, USA; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202, USA.
Sharma RK; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202, USA.
Haribabu B; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202, USA; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202, USA. Electronic address: .
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Źródło :
Seminars in immunology [Semin Immunol] 2017 Oct; Vol. 33, pp. 58-64. Date of Electronic Publication: 2017 Oct 02.
Typ publikacji :
Journal Article; Review; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms :
CD8-Positive T-Lymphocytes/*immunology
Inflammation/*immunology
Leukocytes/*immunology
Leukotriene B4/*metabolism
Neoplasms/*immunology
Receptors, Leukotriene B4/*metabolism
Animals ; Carcinogenesis ; Cell Movement ; Chemotaxis ; Humans ; Mice ; Mice, Knockout ; Signal Transduction ; Xenograft Model Antitumor Assays
Czasopismo naukowe
Tytuł :
Back to the future of targeting leukotriene B 4 mediated inflammation.
Autorzy :
Haribabu B; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202, USA; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202, USA. Electronic address: .
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Źródło :
Seminars in immunology [Semin Immunol] 2017 Oct; Vol. 33, pp. 1-2. Date of Electronic Publication: 2017 Oct 04.
Typ publikacji :
Editorial
MeSH Terms :
Asthma/*drug therapy
Inflammation/*immunology
Leukotriene B4/*metabolism
Neutrophils/*immunology
T-Lymphocytes/*immunology
5-Lipoxygenase-Activating Proteins/metabolism ; Acetates/therapeutic use ; Animals ; Cell Movement ; Chemokines/metabolism ; Epoxide Hydrolases/metabolism ; Humans ; Inflammation/therapy ; Lipid Metabolism ; Molecular Targeted Therapy ; Neutrophil Activation ; Quinolines/therapeutic use
Opinia redakcyjna
Tytuł :
Leukotriene B 4 -receptor-1 mediated host response shapes gut microbiota and controls colon tumor progression.
Autorzy :
Jala VR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY, USA.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY, USA.
Maturu P; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY, USA.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY, USA.
Bodduluri SR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY, USA.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY, USA.
Krishnan E; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY, USA.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY, USA.
Mathis S; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY, USA.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY, USA.
Subbarao K; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY, USA.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY, USA.
Wang M; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY, USA.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY, USA.
Jenson AB; Department of Pathology, University of Louisville Health Sciences Center, Louisville, KY, USA.
Proctor ML; Research Resources Center, University of Louisville Health Sciences Center, Louisville, KY, USA.
Rouchka EC; Department of Computer Engineering & Computer Science, Speed School of Engineering, University of Louisville, Louisville, KY, USA.
Knight R; Center for Microbiome Innovation, University of California San Diego, La Jolla, CA, USA.
Haribabu B; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY, USA.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY, USA.
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Źródło :
Oncoimmunology [Oncoimmunology] 2017 Aug 10; Vol. 6 (12), pp. e1361593. Date of Electronic Publication: 2017 Aug 10 (Print Publication: 2017).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
Czasopismo naukowe
Tytuł :
Microbiota-activated CD103 DCs stemming from microbiota adaptation specifically drive γδT17 proliferation and activation.
Autorzy :
Fleming C; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY, USA.
Cai Y; Department of Medicine, James Graham Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY, USA.
Sun X; Department of Medicine, James Graham Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY, USA.
Jala VR; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY, USA.
Xue F; Department of Medicine, James Graham Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY, USA.
Morrissey S; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY, USA.
Wei YL; Department of Microbiology and Immunology, Stanford University, Stanford, CA, USA.
Chien YH; Department of Microbiology and Immunology, Stanford University, Stanford, CA, USA.
Zhang HG; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY, USA.
Haribabu B; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY, USA.
Huang J; Department of Oncology, Zhejiang University the Second Affiliated Hospital, Hangzhou, China.
Yan J; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY, USA. .; Department of Medicine, James Graham Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY, USA. .; Tumor Immunobiology Program, James Graham Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY, USA. .
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Źródło :
Microbiome [Microbiome] 2017 Apr 24; Vol. 5 (1), pp. 46. Date of Electronic Publication: 2017 Apr 24.
Typ publikacji :
Journal Article
MeSH Terms :
Bacteria/*growth & development
Dendritic Cells/*immunology
Mouth/*microbiology
Th17 Cells/*immunology
Animals ; Antigens, CD/metabolism ; Bacteria/classification ; Bacteria/genetics ; Bacteria/isolation & purification ; DNA, Bacterial/genetics ; DNA, Ribosomal/genetics ; Gastrointestinal Microbiome ; Integrin alpha Chains/metabolism ; Mice ; Mice, Knockout ; Microbiota ; Phylogeny ; RNA, Ribosomal, 16S/genetics ; Receptors, Interleukin-17/genetics ; Sequence Analysis, DNA/methods
Czasopismo naukowe
Tytuł :
Complement C5a Receptor is the Key Initiator of Neutrophil Adhesion Igniting Immune Complex-induced Arthritis.
Autorzy :
Miyabe Y; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Miyabe C; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Murooka TT; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Kim EY; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Newton GA; Vascular Research Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Kim ND; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Haribabu B; James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA.
Luscinskas FW; Vascular Research Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Mempel TR; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Luster AD; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
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Źródło :
Science immunology [Sci Immunol] 2017 Jan; Vol. 2 (7). Date of Electronic Publication: 2017 Jan 20.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Erratum to: Impact of Bi-Axial Shear on Atherogenic Gene Expression by Endothelial Cells.
Autorzy :
Chakraborty A; Department of Chemical Engineering, University of Louisville, Ernst Hall 106, Louisville, KY, 40292, USA.
Chakraborty S; Department of Bioinformatics and Biostatistics, University of Louisville, Louisville, KY, USA.
Jala VR; James Graham Brown Cancer Center and Department of Microbiology & Immunology, University of Louisville, CTRB, Room #324, Louisville, KY, 40202, USA.
Thomas JM; Department of Chemical Engineering, University of Louisville, Ernst Hall 106, Louisville, KY, 40292, USA.
Sharp MK; Department of Mechanical Engineering, University of Louisville, Louisville, KY, USA.
Berson RE; Department of Chemical Engineering, University of Louisville, Ernst Hall 106, Louisville, KY, 40292, USA. .
Haribabu B; James Graham Brown Cancer Center and Department of Microbiology & Immunology, University of Louisville, CTRB, Room #324, Louisville, KY, 40202, USA. .
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Źródło :
Annals of biomedical engineering [Ann Biomed Eng] 2016 Oct; Vol. 44 (10), pp. 3046.
Typ publikacji :
Journal Article; Published Erratum
Czasopismo naukowe
Tytuł :
Impact of Bi-Axial Shear on Atherogenic Gene Expression by Endothelial Cells.
Autorzy :
Chakraborty A; Department of Chemical Engineering, University of Louisville, Ernst Hall 106, Louisville, KY, 40292, USA.
Chakraborty S; Department of Bioinformatics and Biostatistics, University of Louisville, Louisville, KY, USA.
Jala VR; James Graham Brown Cancer Center and Department of Microbiology & Immunology, University of Louisville, CTRB, Room #324, Louisville, KY, 40202, USA.
Thomas JM; Department of Chemical Engineering, University of Louisville, Ernst Hall 106, Louisville, KY, 40292, USA.
Sharp MK; Department of Mechanical Engineering, University of Louisville, Louisville, KY, USA.
Berson RE; Department of Chemical Engineering, University of Louisville, Ernst Hall 106, Louisville, KY, 40292, USA. .
Haribabu B; James Graham Brown Cancer Center and Department of Microbiology & Immunology, University of Louisville, CTRB, Room #324, Louisville, KY, 40202, USA. .
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Źródło :
Annals of biomedical engineering [Ann Biomed Eng] 2016 Oct; Vol. 44 (10), pp. 3032-3045. Date of Electronic Publication: 2016 May 02.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Expression Regulation*
Models, Cardiovascular*
Shear Strength*
Atherosclerosis/*metabolism
Endothelial Cells/*metabolism
Atherosclerosis/pathology ; Atherosclerosis/physiopathology ; Cell Proliferation/drug effects ; E-Selectin/biosynthesis ; Endothelial Cells/pathology ; Humans ; Intercellular Adhesion Molecule-1/biosynthesis ; Interleukin-6/biosynthesis ; Leukotriene B4/pharmacology ; Lipopolysaccharides/toxicity
Czasopismo naukowe
Tytuł :
Chemoattractant Receptors BLT1 and CXCR3 Regulate Antitumor Immunity by Facilitating CD8+ T Cell Migration into Tumors.
Autorzy :
Chheda ZS; James Graham Brown Cancer Center, University of Louisville Health Sciences, Louisville, KY 40202; Department of Microbiology and Immunology, University of Louisville Health Sciences, Louisville, KY 40202;
Sharma RK; James Graham Brown Cancer Center, University of Louisville Health Sciences, Louisville, KY 40202; Division of Medical Oncology, Department of Medicine, University of Louisville Health Sciences, Louisville, KY 40202; and.
Jala VR; James Graham Brown Cancer Center, University of Louisville Health Sciences, Louisville, KY 40202; Department of Microbiology and Immunology, University of Louisville Health Sciences, Louisville, KY 40202;
Luster AD; Division of Rheumatology, Allergy and Immunology, Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02139.
Haribabu B; James Graham Brown Cancer Center, University of Louisville Health Sciences, Louisville, KY 40202; Department of Microbiology and Immunology, University of Louisville Health Sciences, Louisville, KY 40202; .
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Źródło :
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2016 Sep 01; Vol. 197 (5), pp. 2016-26. Date of Electronic Publication: 2016 Jul 27.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation*
CD8-Positive T-Lymphocytes/*physiology
Cell Movement/*immunology
Melanoma, Experimental/*immunology
Receptors, CXCR3/*metabolism
Receptors, Leukotriene B4/*metabolism
Adoptive Transfer ; Animals ; CD8-Positive T-Lymphocytes/immunology ; Chemotaxis, Leukocyte ; Immunotherapy ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Receptors, CXCR3/deficiency ; Receptors, CXCR3/genetics ; Receptors, CXCR3/immunology ; Receptors, Leukotriene B4/deficiency ; Receptors, Leukotriene B4/genetics
Czasopismo naukowe
Tytuł :
Gut Microbiota Conversion of Dietary Ellagic Acid into Bioactive Phytoceutical Urolithin A Inhibits Heme Peroxidases.
Autorzy :
Saha P; Department of Nutritional Sciences, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
Yeoh BS; Department of Nutritional Sciences, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
Singh R; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Chandrasekar B; Institute for Stem Cell Biology and Regenerative Medicine (inStem), UAS-GKVK Campus, Bellary Road, Bangalore, Karnataka, India.
Vemula PK; Institute for Stem Cell Biology and Regenerative Medicine (inStem), UAS-GKVK Campus, Bellary Road, Bangalore, Karnataka, India.; Ramalingaswami ReEntry Fellow, Dept. of Biotechnology, Govt. of India.
Haribabu B; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Vijay-Kumar M; Department of Nutritional Sciences, The Pennsylvania State University, University Park, Pennsylvania, United States of America.; Department of Medicine, The Pennsylvania State University Medical Center, Hershey, Pennsylvania, United States of America.
Jala VR; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
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Źródło :
PloS one [PLoS One] 2016 Jun 02; Vol. 11 (6), pp. e0156811. Date of Electronic Publication: 2016 Jun 02 (Print Publication: 2016).
Typ publikacji :
Journal Article
MeSH Terms :
Diet*
Gastrointestinal Microbiome*/drug effects
Coumarins/*pharmacology
Ellagic Acid/*metabolism
Heme/*metabolism
Peroxidase/*antagonists & inhibitors
Animals ; Biocatalysis/drug effects ; Bone Marrow Cells/cytology ; Coumarins/chemical synthesis ; Coumarins/metabolism ; Edema/pathology ; Humans ; Immunity, Innate/drug effects ; Iron/pharmacology ; Iron Chelating Agents/pharmacology ; Lactoperoxidase/antagonists & inhibitors ; Lactoperoxidase/metabolism ; Lipocalin-2/metabolism ; Mice, Inbred C57BL ; Neutrophils/drug effects ; Neutrophils/metabolism ; Peroxidase/metabolism ; Reactive Oxygen Species/metabolism ; Tetradecanoylphorbol Acetate/pharmacology ; Time Factors
Czasopismo naukowe

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