AP-1转录因子
MMP9公司
生物
哈卡特
c-jun公司
激活剂(遗传学)
激酶
分子生物学
内分泌学
内科学
转录因子
细胞生物学
受体
下调和上调
生物化学
医学
基因
体外
作者
Jiangli Lang,Chen Yang,Lixuan Liu,Li Li,Liangyan Wu,Yanyan Liu,Hengli Luo,Li Yan,Sifan Chen,Jie Ning,Chuan Yang
标识
DOI:10.1016/j.yexcr.2021.112550
摘要
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.
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