信号转导
蛋白激酶B
细胞生物学
化学
MAPK/ERK通路
配体(生物化学)
受体
细胞信号
生物
生物化学
作者
Stine Louise Jeppe Knudsen,Anni Sieu Wai Mac,Lasse Henriksen,Bo van Deurs,Lene Melsæther Grøvdal
标识
DOI:10.3109/08977194.2014.952410
摘要
EGF receptor (EGFR) and its signaling have been investigated for many years, but how its different ligands regulate signaling has not been thoroughly explored. When investigating EGFR activation and downstream signaling in HeLa cells using a panel of ligands, we found a ligand-dependent differential activation of EGFR and the signaling pathways Akt, PLCγ and STAT with HB-EGF and BTC being the most potent ligands. All the tested ligands induced full activation of Erk signaling at 1 nM, whereas only HB-EGF and partly BTC and EGF induced strong activation of Akt, STAT3 and PLCγ at this concentration. Interestingly, we also found that the high activation potencies of HB-EGF and BTC could only partially be explained by their binding affinities, and are therefore likely to be regulated by other mechanisms. We thus suggest that the signaling pathways initiated from the EGFR vary depending on the ligands bound in a cell specific manner.
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