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High glucose activates ERK1/2 to stabilize AP1 and increase MMP9 expression in diabetic foot ulcers.

Authors :
Lang J
Yang C
Liu L
Li L
Wu L
Liu Y
Luo H
Yan L
Chen S
Ning J
Yang C
Source :
Experimental cell research [Exp Cell Res] 2021 Jun 01; Vol. 403 (1), pp. 112550. Date of Electronic Publication: 2021 Mar 03.
Publication Year :
2021

Abstract

Increased matrix metalloproteinase 9 (MMP9) expression is involved in delayed wound healing in diabetic foot ulcers. We created skin wounds in normal SD rats and STZ-induced diabetic SD rats, then we found protein levels of activator protein-1 (AP1), a crucial transcription factor to increase MMP9 transcription, as well as MMP9 was up-regulated in epithelium of diabetic skin tissues. Then, we evaluated the mRNA and protein stability of AP1 subunits C-FOS/C-Jun in HaCaT cells after high glucose treatment. Results showed that high glucose could increase protein stability of C-FOS and C-Jun. Additionally, high glucose also activated extracellular signaling-related kinase 1/2 (ERK1/2). ERK1/2 inhibitor could rescue phosphorylation of C-FOS and C-Jun, increased protein stability of C-Jun, and increased MMP9 expressions. Thus, our study demonstrated that high glucose could activate ERK1/2 to stabilize AP1 and increase MMP9 expression in diabetic skin and HaCaT cells.<br /> (Copyright © 2021. Published by Elsevier Inc.)

Details

Language :
English
ISSN :
1090-2422
Volume :
403
Issue :
1
Database :
MEDLINE
Journal :
Experimental cell research
Publication Type :
Academic Journal
Accession number :
33675806
Full Text :
https://doi.org/10.1016/j.yexcr.2021.112550