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Involvement of RAGE, MAPK and NF‐κB pathways in AGEs‐induced MMP‐9 activation in HaCaT keratinocytes
Author(s) -
Zhu Ping,
Ren Meng,
Yang Chuan,
Hu YongXuan,
Ran JianMin,
Yan Li
Publication year - 2012
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.1600-0625.2011.01408.x
Subject(s) - hacat , rage (emotion) , mapk/erk pathway , glycation , p38 mitogen activated protein kinases , kinase , matrix metalloproteinase , signal transduction , protein kinase a , chemistry , microbiology and biotechnology , cancer research , biology , receptor , biochemistry , in vitro , neuroscience
Advanced glycation end products (AGEs) exert divergent effects on the pathogenesis of diabetes complications. Excessive expression of matrix metalloproteinases‐9 (MMP‐9) is deleterious to the cutaneous wound‐healing process in the context of diabetes. However, the effect of AGEs on MMP‐9 induction in skin cells and the exact molecular mechanisms involved are still poorly understood. In this study, we investigated the effect of AGEs on the production of MMP‐9 in HaCaT keratinocytes and characterized the signal transduction pathways activated by AGEs that are involved in MMP‐9 regulation. We showed that AGE–BSA increased MMP‐9 expression in HaCaT cells at both the protein and mRNA levels. The stimulatory effect of AGE–BSA on MMP‐9 was attenuated by inhibitors of extracellular‐signal‐regulated kinase (ERK1/2, U0126), p38 mitogen‐activated protein kinase (MAPK, SB203580) and NF‐κB, but not c‐Jun N‐terminal kinase. Furthermore, receptor for advanced glycation end products (RAGE) was expressed in keratinocytes, and incubation with AGE–BSA resulted in a significant upregulation of RAGE expression in a dose‐dependent manner. Silencing of the RAGE gene prevented AGE–BSA‐induced MMP‐9 activation and the phosphorylation of ERK1/2 and p38 MAPK. We also observed the involvement of NF‐κB in AGE–BSA‐induced MMP‐9 activation, which was not blocked by U0126 and SB203580. These results suggest that AGEs may play an important role in the impairment of diabetic wound healing by upregulating MMP‐9 expression in keratinocytes via the RAGE, ERK1/2 and p38 MAPK pathways; activation of NF‐κB is also involved in this process. These pathways may represent potential targets for drug interventions to improve diabetic wound healing, a process in which MMP‐9 plays a critical role.