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溶血磷脂酸(LPA)通过抑制线粒体途径保护肠上皮细胞免于凋亡。

LPA protects intestinal epithelial cells from apoptosis by inhibiting the mitochondrial pathway.

作者信息

Deng Wenlin, Wang De-An, Gosmanova Elvira, Johnson Leonard R, Tigyi Gabor

机构信息

Department of Physiology, University of Tennessee Health Sciences Center, Memphis, Tennessee 38163, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2003 May;284(5):G821-9. doi: 10.1152/ajpgi.00406.2002.

Abstract

We previously showed (Gastroenterology 123: 206-216, 2002) that lysophosphatidic acid (LPA) protects and rescues rat intestinal epithelial cells (IEC-6) from apoptosis. Here, we provide evidence for the LPA-elicited inhibition of the mitochondrial apoptotic pathway leading to attenuation of caspase-3 activation. Pretreatment of IEC-6 cells with LPA inhibited campothecin-induced caspase-9 and caspase-3 activation and DNA fragmentation. A caspase-9 inhibitor peptide mimicked the LPA-elicited antiapoptotic activity. LPA elicited ERK1/ERK2 and PKB/Akt phosphorylation. The LPA-elicited antiapoptotic activity and inhibition of caspase-9 activity were abrogated by pertussis toxin, PD 98059, wortmannin, and LY 294002. LPA reduced cytochrome c release from mitochondria and prevented activation of caspase-9. LPA prevented translocation of Bax from cytosol to mitochondria and increased the expression of the antiapoptotic Bcl-2 mRNA and protein. LPA had no effect on Bcl-xl, Bad, and Bak mRNA or protein expression. These data indicate that LPA protects IEC-6 cells from camptothecin-induced apoptosis through G(i)-coupled inhibition of caspase-3 activation mediated by the attenuation of caspase-9 activation due to diminished cytochrome c release, involving upregulation of Bcl-2 protein expression and prevention of Bax translocation.

摘要

我们之前曾表明(《胃肠病学》123: 206 - 216, 2002)溶血磷脂酸(LPA)可保护大鼠肠上皮细胞(IEC - 6)并使其免于凋亡。在此,我们提供证据表明LPA可抑制线粒体凋亡途径,从而导致半胱天冬酶 - 3激活减弱。用LPA预处理IEC - 6细胞可抑制喜树碱诱导的半胱天冬酶 - 9和半胱天冬酶 - 3激活以及DNA片段化。一种半胱天冬酶 - 9抑制肽模拟了LPA引发的抗凋亡活性。LPA可引发细胞外信号调节激酶1/细胞外信号调节激酶2(ERK1/ERK2)和蛋白激酶B/蛋白激酶B(PKB/Akt)磷酸化。百日咳毒素、PD 98059、渥曼青霉素和LY 294002可消除LPA引发的抗凋亡活性和对半胱天冬酶 - 9活性的抑制。LPA减少了细胞色素c从线粒体的释放并阻止了半胱天冬酶 - 9的激活。LPA阻止了Bax从细胞质向线粒体的转位,并增加了抗凋亡蛋白Bcl - 2 mRNA和蛋白的表达。LPA对Bcl - xl、Bad和Bak的mRNA或蛋白表达没有影响。这些数据表明,LPA通过G(i)偶联抑制半胱天冬酶 - 3激活来保护IEC - 6细胞免受喜树碱诱导的凋亡,该抑制作用是由于细胞色素c释放减少导致半胱天冬酶 - 9激活减弱介导的,涉及Bcl - 2蛋白表达上调和Bax转位的阻止。

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