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Tytuł pozycji:

Wharton's Jelly Mesenchymal Stem Cell-Derived Extracellular Vesicles Reduce SARS-CoV2-Induced Inflammatory Cytokines Under High Glucose and Uremic Toxin Conditions.

Tytuł:
Wharton's Jelly Mesenchymal Stem Cell-Derived Extracellular Vesicles Reduce SARS-CoV2-Induced Inflammatory Cytokines Under High Glucose and Uremic Toxin Conditions.
Autorzy:
Khanh VC; Laboratory of Regenerative Medicine and Stem Cell Biology, Departments of University of Tsukuba, Tsukuba, Japan.
Fukushige M; Laboratory of Regenerative Medicine and Stem Cell Biology, Departments of University of Tsukuba, Tsukuba, Japan.
Chang YH; Laboratory of Regenerative Medicine and Stem Cell Biology, Departments of University of Tsukuba, Tsukuba, Japan.
Hoang NN; Laboratory of Regenerative Medicine and Stem Cell Biology, Departments of University of Tsukuba, Tsukuba, Japan.
Yamashita T; Laboratory of Regenerative Medicine and Stem Cell Biology, Departments of University of Tsukuba, Tsukuba, Japan.
Obata-Yasuoka M; Obstetrics and Gynecology, University of Tsukuba, Tsukuba, Japan.
Hamada H; Obstetrics and Gynecology, University of Tsukuba, Tsukuba, Japan.
Osaka M; Cardiovascular Surgery, University of Tsukuba, Tsukuba, Japan.
Hiramatsu Y; Cardiovascular Surgery, University of Tsukuba, Tsukuba, Japan.
Ohneda O; Laboratory of Regenerative Medicine and Stem Cell Biology, Departments of University of Tsukuba, Tsukuba, Japan.
Źródło:
Stem cells and development [Stem Cells Dev] 2021 Aug 01; Vol. 30 (15), pp. 758-772. Date of Electronic Publication: 2021 Jul 05.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't; Systematic Review
Język:
English
Imprint Name(s):
Original Publication: Larchmont, NY : Mary Ann Liebert, Inc., c2004-
MeSH Terms:
Cytokine Release Syndrome/*prevention & control
Extracellular Vesicles/*physiology
Mesenchymal Stem Cells/*cytology
SARS-CoV-2/*physiology
Wharton Jelly/*cytology
Adult ; Aged ; COVID-19/blood ; COVID-19/complications ; COVID-19/metabolism ; COVID-19/therapy ; Cells, Cultured ; Coculture Techniques ; Cytokine Release Syndrome/genetics ; Cytokine Release Syndrome/metabolism ; Cytokine Release Syndrome/virology ; Cytokines/genetics ; Cytokines/metabolism ; Diabetes Complications/blood ; Diabetes Complications/metabolism ; Diabetes Complications/therapy ; Diabetes Complications/virology ; Diabetes Mellitus/blood ; Diabetes Mellitus/metabolism ; Diabetes Mellitus/therapy ; Diabetes Mellitus/virology ; Dose-Response Relationship, Drug ; Female ; Gene Expression Regulation/drug effects ; Glucose/metabolism ; Glucose/pharmacology ; Humans ; Inflammation Mediators/metabolism ; Male ; Mesenchymal Stem Cell Transplantation ; Mesenchymal Stem Cells/physiology ; Pregnancy ; Toxins, Biological/metabolism ; Toxins, Biological/pharmacology ; Umbilical Cord/cytology ; Uremia/blood ; Uremia/complications ; Uremia/metabolism ; Uremia/therapy
References:
Stem Cells Int. 2019 Mar 6;2019:7012692. (PMID: 30956673)
Nat Rev Immunol. 2020 Jul;20(7):397-398. (PMID: 32457522)
Stem Cells Transl Med. 2019 Sep;8(9):880-886. (PMID: 31045328)
Sci Transl Med. 2020 Apr 29;12(541):. (PMID: 32253226)
Aging Dis. 2020 Mar 9;11(2):216-228. (PMID: 32257537)
Int J Mol Med. 2013 Oct;32(4):795-804. (PMID: 23942780)
Stem Cells Int. 2019 Feb 26;2019:5126156. (PMID: 30936922)
Front Immunol. 2020 Sep 24;11:558898. (PMID: 33072097)
Int J Stem Cells. 2016 May 30;9(1):124-36. (PMID: 27426094)
Cell Mol Immunol. 2016 Jan;13(1):3-10. (PMID: 26189369)
PLoS One. 2020 Nov 18;15(11):e0241541. (PMID: 33206661)
Circulation. 2002 Oct 15;106(16):2067-72. (PMID: 12379575)
Circ Res. 2007 Aug 31;101(5):455-64. (PMID: 17626897)
Stem Cell Res Ther. 2018 Jan 29;9(1):17. (PMID: 29378639)
Front Cell Dev Biol. 2020 Mar 12;8:149. (PMID: 32226787)
Cell Rep. 2021 Apr 6;35(1):108959. (PMID: 33811811)
Commun Biol. 2022 Jan 12;5(1):45. (PMID: 35022513)
Trends Pharmacol Sci. 2020 Sep;41(9):653-664. (PMID: 32709406)
Clin J Am Soc Nephrol. 2020 Aug 7;15(8):1087-1089. (PMID: 32636199)
Stem Cells Dev. 2020 Jun 15;29(12):747-754. (PMID: 32380908)
Stem Cells Dev. 2014 Mar 1;23(5):488-501. (PMID: 24171667)
Rev Invest Clin. 2020;72(3):151-158. (PMID: 32584330)
Diabetes Metab Syndr. 2020 Jul - Aug;14(4):395-403. (PMID: 32334395)
Clin J Am Soc Nephrol. 2020 Aug 7;15(8):1139-1145. (PMID: 32444393)
Nat Rev Immunol. 2020 Jun;20(6):355-362. (PMID: 32376901)
Proc Natl Acad Sci U S A. 2020 May 26;117(21):11727-11734. (PMID: 32376634)
PLoS One. 2020 Dec 7;15(12):e0243191. (PMID: 33284825)
Clin J Am Soc Nephrol. 2020 Aug 7;15(8):1174-1178. (PMID: 32423908)
Stem Cell Reports. 2021 Mar 9;16(3):419-427. (PMID: 32950067)
Lancet Diabetes Endocrinol. 2020 Sep;8(9):782-792. (PMID: 32687793)
J Immunol Res. 2018 Sep 6;2018:2180373. (PMID: 30271792)
J Infect. 2020 Jun;80(6):607-613. (PMID: 32283152)
Proc Natl Acad Sci U S A. 2020 May 19;117(20):10970-10975. (PMID: 32350134)
Inflammopharmacology. 2021 Feb;29(1):91-100. (PMID: 33159646)
Toxins (Basel). 2017 Mar 23;9(4):. (PMID: 28333114)
Lancet Diabetes Endocrinol. 2020 Oct;8(10):813-822. (PMID: 32798472)
Clin Exp Nephrol. 2019 Feb;23(2):151-157. (PMID: 29869756)
Stem Cells Transl Med. 2016 Sep;5(9):1190-203. (PMID: 27496568)
Stem Cell Res Ther. 2018 Mar 9;9(1):63. (PMID: 29523213)
J Virol Methods. 2011 Jun;174(1-2):144-9. (PMID: 21458491)
J Diabetes Sci Technol. 2020 Jul;14(4):813-821. (PMID: 32389027)
Diabetes. 2020 Dec;69(12):2691-2699. (PMID: 33024003)
Diabetes Care. 2009 Nov;32 Suppl 2:S194-8. (PMID: 19875551)
Cell. 2020 Apr 16;181(2):271-280.e8. (PMID: 32142651)
Nat Methods. 2012 Jul;9(7):671-5. (PMID: 22930834)
Signal Transduct Target Ther. 2017;2:. (PMID: 29158945)
Nat Med. 2020 Oct;26(10):1636-1643. (PMID: 32839624)
Front Immunol. 2020 Jul 10;11:1648. (PMID: 32754159)
Diabetes. 2005 Jun;54(6):1615-25. (PMID: 15919781)
Nat Rev Nephrol. 2020 Dec;16(12):705-706. (PMID: 32848205)
Contributed Indexing:
Keywords: Calu-3 cells; DM; RD; SARS-CoV-2; cytokine storm; extracellular vesicles
Substance Nomenclature:
0 (Cytokines)
0 (Inflammation Mediators)
0 (Toxins, Biological)
0 (uremia middle molecule toxins)
IY9XDZ35W2 (Glucose)
Entry Date(s):
Date Created: 20210602 Date Completed: 20210811 Latest Revision: 20240403
Update Code:
20240403
PubMed Central ID:
PMC8356045
DOI:
10.1089/scd.2021.0065
PMID:
34074129
Czasopismo naukowe
Cytokine storm is recognized as one of the factors contributing to organ failures and mortality in patients with COVID-19. Due to chronic inflammation, COVID-19 patients with diabetes mellitus (DM) or renal disease (RD) have more severe symptoms and higher mortality. However, the factors that contribute to severe outcomes of COVID-19 patients with DM and RD have received little attention. In an effort to investigate potential treatments for COVID-19, recent research has focused on the immunomodulation functions of mesenchymal stem cells (MSCs). In this study, the correlation between DM and RD and the severity of COVID-19 was examined by a combined approach with a meta-analysis and experimental research. The results of a systematic review and meta-analysis suggested that the odd of mortality in patients with both DM and RD was increased in comparison to those with a single comorbidity. In addition, in the experimental research, the data showed that high glucose and uremic toxins contributed to the induction of cytokine storm in human lung adenocarcinoma epithelial cells (Calu-3 cells) in response to SARS-CoV Peptide Pools. Of note, the incorporation of Wharton's jelly MSC-derived extracellular vesicles (WJ-EVs) into SARS-CoV peptide-induced Calu-3 resulted in a significant decrease in nuclear NF-κB p65 and the downregulation of the cytokine storm under high concentrations of glucose and uremic toxins. This clearly suggests the potential for WJ-EVs to reduce cytokine storm reactions in patients with both chronic inflammation diseases and viral infection.

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