Wang Yinna, Vodovotz Yoram, Kim Peter K M, Zamora Ruben, Billiar Timothy R
Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Ann N Y Acad Sci. 2002 May;962:415-22. doi: 10.1111/j.1749-6632.2002.tb04085.x.
Nitric oxide (NO) exerts numerous antiapoptotic effects on hepatocytes in settings of inflammation and tissue damage. These actions of NO are modulated by a variety of mechanisms under both physiologic and pathologic conditions. Nitric oxide inhibits cell death or apoptosis by modulation of heat shock proteins, S-nitrosylation of caspases at their catalytic site cysteine residue, triggering of the cGMP pathway, and prevention of mitochondrial dysfunction. Our preliminary studies also suggest that NO can modulate apoptosis-related genes in a manner consistent with an antiapoptotic effect. This review focuses on these molecular mechanisms of cytoprotection by NO.
一氧化氮(NO)在炎症和组织损伤情况下对肝细胞发挥多种抗凋亡作用。在生理和病理条件下,NO的这些作用通过多种机制进行调节。一氧化氮通过调节热休克蛋白、在半胱天冬酶催化位点的半胱氨酸残基上进行S-亚硝基化、触发cGMP途径以及预防线粒体功能障碍来抑制细胞死亡或凋亡。我们的初步研究还表明,NO可以以与抗凋亡作用一致的方式调节凋亡相关基因。本综述重点关注NO细胞保护作用的这些分子机制。