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Advanced glycation endproducts stimulate the MAP‐kinase pathway in tubulus cell line LLC‐PK 1
Author(s) -
Simm Andreas,
Münch Gerald,
Seif Farshid,
Schenk Oliver,
Heidland August,
Richter Hedwig,
Vamvakas Spiridou,
Schinzel Reinhard
Publication year - 1997
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(97)00644-3
Subject(s) - signal transduction , phosphorylation , chemistry , microbiology and biotechnology , kinase , dephosphorylation , glycation , biochemistry , biology , receptor , phosphatase
Advanced glycation endproducts (AGEs) are suggested to play an important role in diabetic nephropathy. They induce specific cellular responses such as the release of cytokines in different cell lines. The effect of AGEs on signal transduction pathways was investigated in the renal tubulus cell line LLC‐PK 1 . Using a serine‐phosphate‐specific antibody AGE‐induced cellular responses associated with phosphorylation/dephosphorylation events were demonstrated. In particular, the p42 MAP kinase and its downstream target, the AP‐1 complex, are shown to be activated by AGE‐BSA but not by BSA. In contrast, only partial phosphorylation is observed for the p70 S6 ‐kinase. Thus, AGEs appear to induce specific signal transduction pathways.