Tracz Michal J, Alam Jawed, Nath Karl A
Mayo Clinic, 200 First Street, SW, Guggenheim 542, Rochester, MN 55905, USA.
J Am Soc Nephrol. 2007 Feb;18(2):414-20. doi: 10.1681/ASN.2006080894. Epub 2007 Jan 17.
An iron-containing, tetrapyrrole ring, heme is an essential prosthetic group in an array of proteins that comprehensively affect cellular function and metabolism; yet "free" heme in sufficient amounts can be damaging to the kidney and other organs because of its bioreactivity and pro-oxidant effects. This review discusses the cellular metabolism of heme in health and disease and covers such areas as the synthesis of heme and its utilization in heme proteins; mechanisms underlying the toxicity of heme; and the extent to which pathophysiologic processes, such as renal incorporation of heme proteins or destabilization of intracellular heme proteins, increase intracellular levels of heme and provoke renal injury. The main catabolic process that degrades heme, the heme oxygenase (HO) system, is reviewed, and evidence for the protective effects of HO-1 against acute and chronic heme/heme protein-induced renal injury is summarized. Finally, current views regarding the molecular basis for heme-induced upregulation of HO-1 are discussed.
血红素是一种含铁的四吡咯环,是一系列蛋白质中必不可少的辅基,这些蛋白质全面影响细胞功能和代谢;然而,大量“游离”血红素因其生物反应性和促氧化作用,可能对肾脏和其他器官造成损害。本文综述了健康和疾病状态下血红素的细胞代谢,涵盖血红素的合成及其在血红素蛋白中的利用等领域;血红素毒性的潜在机制;以及病理生理过程(如血红素蛋白的肾脏摄取或细胞内血红素蛋白的不稳定)在多大程度上增加细胞内血红素水平并引发肾损伤。本文回顾了降解血红素的主要分解代谢过程——血红素加氧酶(HO)系统,并总结了HO-1对急性和慢性血红素/血红素蛋白诱导的肾损伤的保护作用的证据。最后,讨论了目前关于血红素诱导HO-1上调的分子基础的观点。