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首页> 外文期刊>Wound repair and regeneration: official publication of the Wound Healing Society [and] the European Tissue Repair Society >Preconditioning with cobalt protoporphyrin protects human gastric mucosal cells from deoxycholate-induced apoptosis.
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Preconditioning with cobalt protoporphyrin protects human gastric mucosal cells from deoxycholate-induced apoptosis.

机译:预处理与钴原卟啉保护人类的胃粘膜细胞deoxycholate-induced细胞凋亡。

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摘要

In this study, a known inducer of heme oxygenase-1 (HO-1) expression, cobalt protoporphyrin, and the introduction of a recombinant plasmid expressing HO-1 were examined for their ability to protect gastric epithelial cells from deoxycholate-induced injury. Physiologic levels of the secondary bile salt induce apoptosis in a human gastric adenocarcinoma mucosal cell line. Cobalt protoporphyrin induced expression of HO-1 protein with maximal levels attaining a plateau at 48 hours. Pretreatment with cobalt protoporphyrin before challenge with 200 muM deoxycholate inhibited cell death, DNA fragmentation, the appearance of cytosolic nucleosomes, and cleavage of caspase-3, caspase-9, and poly-(ADP-ribose) polymerase 1. Similarly, expression of HO-1 by introduction of a recombinant plasmid also showed a resistance to deoxycholate-induced apoptosis. These results implicate a possible role for HO-1 in modulating apoptosis in gastric epithelial cells.
机译:在这项研究中,一种已知的血红素oxygenase-1诱导物(HO-1)表达式,钴原卟啉,引入重组质粒表达HO-1检查保护的能力胃上皮细胞从deoxycholate-induced受伤。继发性胆汁盐诱导的细胞凋亡人类腺癌胃粘膜细胞线。钴HO-1的原卟啉诱导表达蛋白质与最大水平达到一个高原在48小时内。200年挑战前原卟啉妈妈脱氧胆酸盐抑制细胞死亡,DNA胞质分裂,出现核小体,caspase-3乳沟,(caspase-9,保利)- ADP-ribose聚合酶1。同样,HO-1表达式的引入重组质粒还显示阻力deoxycholate-induced细胞凋亡。暗示可能HO-1的调制作用在胃上皮细胞凋亡。

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