Back to Search
Start Over
High glucose activates ERK1/2 to stabilize AP1 and increase MMP9 expression in diabetic foot ulcers.
- 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.)
- Subjects :
- Animals
Diabetes Mellitus drug therapy
Diabetic Foot metabolism
Humans
JNK Mitogen-Activated Protein Kinases drug effects
JNK Mitogen-Activated Protein Kinases metabolism
MAP Kinase Signaling System drug effects
Mitogen-Activated Protein Kinases drug effects
Mitogen-Activated Protein Kinases metabolism
Rats, Sprague-Dawley
Signal Transduction drug effects
Transcription Factor AP-1 drug effects
Up-Regulation drug effects
Rats
Diabetic Foot drug therapy
Glucose pharmacology
Matrix Metalloproteinase 9 metabolism
Transcription Factor AP-1 metabolism
Subjects
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