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首页> 外文期刊>American Journal of Physiology >Increased in vitro activation of EGFR by membrane-bound TGF-alpha from gastric and colonic mucosa of aged rats.
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Increased in vitro activation of EGFR by membrane-bound TGF-alpha from gastric and colonic mucosa of aged rats.

机译:膜结合的TGF-α对衰老大鼠胃和结肠黏膜的EGFR体外活化作用增强。

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Although aging is associated with increased epidermal growth factor receptor (EGFR) tyrosine kinase activity in Fischer 344 rat gastric and colonic mucosa, the regulatory mechanisms for the age-related rise in EGFR tyrosine kinase are poorly understood. Transmembrane transforming growth factor-alpha (TGF-alpha) may modulate EGFR function through an autocrine/juxtacrine mechanism. The present study aimed to determine the contribution of membrane-bound precursors of TGF-alpha in enhancing EGFR activation in the gastric and colonic mucosa during aging. The extent of EGFR tyrosine phosphorylation, a measure of EGFR activation, was substantially higher (300--350%) in the gastric and colonic mucosa of 23- (aged) vs. 4-mo-old (young) Fischer 344 rats. This was accompanied by an increase (200--1,000%) in the relative concentration of 18- to 20-kDa membrane-bound precursor forms of TGF-alpha. The amount of TGF-alpha bound to EGFR was also higher (150-250%) in the gastric and colonic mucosa of aged vs. young rats. In vitro studies revealed that exposure of HCT 116 cells (a colon cancer cell line) to TGF-alpha from gastric and colonic mucosal membranes of aged rats caused a 200--250% higher activation of EGFR and extracellular signal-related kinases (p42/44) compared with young rats. Our data suggest that the membrane-bound precursor form(s) of TGF-alpha may partly be responsible for enhancing EGFR activation in the gastric and colonic mucosa of aged rats, probably though an autocrine/juxtacrine mechanism(s).
机译:尽管衰老与Fischer 344大鼠胃和结肠粘膜中表皮生长因子受体(EGFR)酪氨酸激酶活性增加有关,但对与年龄相关的EGFR酪氨酸激酶升高的调节机制了解甚少。跨膜转化生长因子-α(TGF-α)可能通过自分泌/邻分泌机制调节EGFR功能。本研究旨在确定TGF-α的膜结合前体在衰老过程中增强胃和结肠粘膜中EGFR活化的作用。 23岁(年龄)的胃和结肠黏膜中的EGFR酪氨酸磷酸化程度显着更高(300--350%),而4个月大(年轻)的Fischer 344大鼠则更高。这伴随着TGF-α的18至20 kDa膜结合前体形式的相对浓度增加(200--1,000%)。与年轻大鼠相比,老年大鼠的胃和结肠粘膜中与EGFR结合的TGF-α的含量也更高(150-250%)。体外研究表明,HCT 116细胞(结肠癌细胞系)暴露于老年大鼠胃和结肠粘膜的TGF-α会导致EGFR和细胞外信号相关激酶的激活率提高200--250%(p42 / 44)与幼鼠相比。我们的数据表明,TGF-α的膜结合前体形式可能部分负责增强衰老大鼠的胃和结肠粘膜中的EGFR活化,可能是通过自分泌/邻分泌机制引起的。

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