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Tytuł pozycji:

Vaccarin Regulates Diabetic Chronic Wound Healing through FOXP2/AGGF1 Pathways.

Tytuł:
Vaccarin Regulates Diabetic Chronic Wound Healing through FOXP2/AGGF1 Pathways.
Autorzy:
Liu Y; Department of Basic Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi 214122, China.
Sun J; Department of Basic Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi 214122, China.
Ma X; Department of Basic Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi 214122, China.
Li S; Department of Basic Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi 214122, China.
Ai M; Department of Basic Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi 214122, China.
Xu F; Department of Basic Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi 214122, China.
Qiu L; Department of Basic Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi 214122, China.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2020 Mar 13; Vol. 21 (6). Date of Electronic Publication: 2020 Mar 13.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Basel, Switzerland : MDPI, [2000-
MeSH Terms:
Wound Healing*
Angiogenic Proteins/*metabolism
Diabetes Mellitus, Experimental/*complications
Flavonoids/*therapeutic use
Forkhead Transcription Factors/*metabolism
Glycosides/*therapeutic use
Pressure Ulcer/*drug therapy
Repressor Proteins/*metabolism
Angiogenic Proteins/genetics ; Animals ; Cell Movement ; Cell Proliferation ; Cells, Cultured ; Endothelial Cells/drug effects ; Endothelial Cells/metabolism ; Endothelial Cells/physiology ; Endothelium, Vascular/cytology ; Flavonoids/pharmacology ; Forkhead Transcription Factors/genetics ; Glycosides/pharmacology ; Humans ; MAP Kinase Signaling System ; Male ; Mice ; Mice, Inbred C57BL ; Pressure Ulcer/etiology ; Pressure Ulcer/metabolism ; Repressor Proteins/genetics
References:
Mater Sci Eng C Mater Biol Appl. 2016 Feb;59:303-309. (PMID: 26652377)
Int J Mol Med. 2015 Jan;35(1):135-42. (PMID: 25352009)
J Cancer. 2017 Aug 2;8(13):2501-2510. (PMID: 28900488)
Mol Ther Nucleic Acids. 2018 Mar 2;10:331-348. (PMID: 29499945)
Arch Biochem Biophys. 2007 Sep 1;465(1):164-71. (PMID: 17597576)
Nature. 2004 Feb 12;427(6975):640-5. (PMID: 14961121)
Diabetologia. 2008 May;51(5):747-55. (PMID: 18297261)
PLoS One. 2017 Jan 3;12(1):e0168937. (PMID: 28045948)
Med Arch. 2018 Dec;72(6):444-448. (PMID: 30814778)
Hum Mol Genet. 2016 Dec 1;25(23):5094-5110. (PMID: 27522498)
Int J Mol Sci. 2019 Sep 17;20(18):. (PMID: 31533227)
Cell Signal. 2013 May;25(5):1126-35. (PMID: 23403124)
J Pharmacol Exp Ther. 2016 Feb;356(2):324-32. (PMID: 26567319)
Biomed Pharmacother. 2017 Nov;95:144-152. (PMID: 28841454)
J Invest Dermatol. 2011 Nov;131(11):2316-22. (PMID: 21833012)
Diabetes. 2019 Aug;68(8):1635-1648. (PMID: 31092480)
Eur J Pharmacol. 2019 May 15;851:13-24. (PMID: 30779918)
Exp Cell Res. 2016 Jul 1;345(1):25-36. (PMID: 27208585)
Curr Cancer Drug Targets. 2018;18(4):382-389. (PMID: 29484998)
Eur J Pharmacol. 2018 Jan 5;818:371-380. (PMID: 29128366)
Biomed Chromatogr. 2014 Dec;28(12):1789-94. (PMID: 24802257)
Handb Clin Neurol. 2014;126:97-107. (PMID: 25410217)
Hum Mol Genet. 2013 Mar 1;22(5):963-76. (PMID: 23197652)
J Pharmacol Toxicol Methods. 2018 Mar - Apr;90:13-18. (PMID: 29100964)
Cell Signal. 2013 Aug;25(8):1645-53. (PMID: 23628701)
World J Diabetes. 2015 Feb 15;6(1):37-53. (PMID: 25685277)
J Biol Chem. 2009 Aug 28;284(35):23331-43. (PMID: 19556247)
Mol Neurobiol. 2018 Dec;55(12):9089-9099. (PMID: 29637443)
Skelet Muscle. 2017 Oct 10;7(1):20. (PMID: 29017538)
Cardiovasc Diabetol. 2015 Feb 18;14:26. (PMID: 25888905)
Curr Pharm Des. 2005;11(18):2301-9. (PMID: 16022669)
Mol Med Rep. 2016 Mar;13(3):2143-50. (PMID: 26795539)
Angiogenesis. 2018 Aug;21(3):425-532. (PMID: 29766399)
Diabetologia. 2015 Aug;58(8):1836-44. (PMID: 26021489)
Exp Cell Res. 2015 Oct 1;337(2):146-59. (PMID: 25882498)
J Wound Care. 2001 Jul;10(7):281-7. (PMID: 12964349)
BMC Pharmacol Toxicol. 2017 Aug 30;18(1):62. (PMID: 28854981)
Int J Mol Med. 2014 Apr;33(4):833-9. (PMID: 24452195)
Oncol Rep. 2018 Feb;39(2):731-738. (PMID: 29207173)
Grant Information:
K2050205 Jiangnan University Youth Fund 2018; WX18IIAN010 Wuxi Municipal Bureau on Science and Technology; BK20190597 Natural Science Foundation of Jiangsu Province; 2019M661729 Chinese Postdoctoral Science Fund; JUFSTR20180101 national first-class discipline program of Food Science and Technology; JUSRP11754 Fundamental Research Funds for the Central Universities
Contributed Indexing:
Keywords: AGGF1; FOXP2; T1DM; diabetic chronic wounds; vaccarin
Substance Nomenclature:
0 (Aggf1 protein, mouse)
0 (Angiogenic Proteins)
0 (Flavonoids)
0 (Forkhead Transcription Factors)
0 (Foxp2 protein, mouse)
0 (Glycosides)
0 (Repressor Proteins)
0 (vaccarin H)
Entry Date(s):
Date Created: 20200319 Date Completed: 20201201 Latest Revision: 20201201
Update Code:
20240105
PubMed Central ID:
PMC7139532
DOI:
10.3390/ijms21061966
PMID:
32183046
Czasopismo naukowe
Background: Diabetes mellitus is a growing global health issue nearly across the world. Diabetic patients who are prone to develop diabetes-related complications often exhibit progressive neuropathy (painless and sensory loss). It is usual for small wounds to progress to ulceration, which especially worsens with peripheral arterial disease and in the presence of anaerobic bacteria, culminating into gangrene. In our study, vaccarin (VAC), the main active monomer extracted from Chinese herb vaccariae semen , is proven to have a role in promoting diabetic chronic wound healing through a cytoprotective role under high glucose conditions.
Materials and Methods: We constructed a pressure ulcer on both VAC-treated and control mice based on a type 1 diabetes (T1DM) model. The wound healing index was evaluated by an experimental wound assessment tool (EWAT). We also determined the effect of VAC on the proliferation and cell migration of human microvascular endothelial cells (HMEC-1) by a cell counting kit (CCK-8), a scratch and transwell assay.
Results: The results demonstrated that VAC could promote the proliferation and migration of high glucose-stimulated HMEC-1 cells, which depend on the activation of FOXP2/AGGF1. Activation of the angiogenic factor with G patch and FHA domains 1 (AGGF1) caused enhanced phosphorylation of serine/threonine kinase (Akt) and extracellular regulated protein kinases (Erk1/2). By silencing the expression of forkhead box p2 (FOXP2) protein by siRNA, both mRNA and protein expression of AGGF1 were downregulated, leading to a decreased proliferation and migration of HMEC-1 cells. In addition, a diabetic chronic wound model in vivo unveiled that VAC had a positive effect on chronic wound healing, which involved the activation of the above-mentioned pathways.
Conclusions: In summary, our study found that VAC promoted chronic wound healing in T1DM mice by activating the FOXP2/AGGF1 pathway, indicating that VAC may be a promising candidate for the treatment of the chronic wounds of diabetic patients.
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