Xie Jun, Guo Qing
Department of Physiology, The University of Oklahoma Health Sciences Center, 940 Stanton L. Young Boulevard, Oklahoma City, OK 73104, USA.
J Am Soc Nephrol. 2006 Dec;17(12):3336-46. doi: 10.1681/ASN.2006040311. Epub 2006 Oct 25.
Apoptosis antagonizing transcription factor (AATF) is a leucine zipper domain-containing protein that has antiapoptotic properties. AATF is expressed in several organs and tissues, including the kidney. AATF may participate in inhibition of proapoptotic pathways and/or activation of antiapoptotic pathways. Ischemia/reperfusion-induced renal injury (IRI) is clinically important because it typically damages renal tubular epithelial cells and glomerular cells and is the most common cause of acute renal failure. It now is reported that AATF is expressed in human kidney proximal tubule (HK-2) cells and in mouse primary renal tubule epithelial cells. Levels of AATF expression were altered significantly in these cells in a well-established in vitro model of renal IRI. In transfected HK-2 cells, RNA interference-mediated silencing of AATF exacerbated whereas overexpression of the full-length AATF ameliorated mitochondrial dysfunction, accumulation of superoxide and peroxynitrite, lipid peroxidation, caspase-3 activation, and apoptotic death that were induced by IRI. In primary renal tubule epithelial cells, overexpression of AATF mediated by recombinant adeno-associated virus (AAV) vectors resulted in significant antiapoptotic activity, whereas knockdown of AATF by small interference RNA led to exacerbated cell death after IRI. These results identify AATF as a novel cytoprotective factor against oxidative and apoptotic damage in renal tubular cells. AATF may represent a potential candidate for therapeutic application in IRI.
凋亡拮抗转录因子(AATF)是一种含有亮氨酸拉链结构域的蛋白质,具有抗凋亡特性。AATF在包括肾脏在内的多个器官和组织中表达。AATF可能参与抑制促凋亡途径和/或激活抗凋亡途径。缺血/再灌注诱导的肾损伤(IRI)在临床上很重要,因为它通常会损害肾小管上皮细胞和肾小球细胞,是急性肾衰竭最常见的原因。现在有报道称,AATF在人肾近端小管(HK-2)细胞和小鼠原代肾小管上皮细胞中表达。在一个成熟的肾IRI体外模型中,这些细胞中AATF的表达水平发生了显著变化。在转染的HK-2细胞中,RNA干扰介导的AATF沉默会加剧IRI诱导的线粒体功能障碍、超氧化物和过氧亚硝酸盐的积累、脂质过氧化、caspase-3激活以及凋亡死亡,而全长AATF的过表达则会改善这些情况。在原代肾小管上皮细胞中,重组腺相关病毒(AAV)载体介导的AATF过表达具有显著的抗凋亡活性,而小干扰RNA敲低AATF则会导致IRI后细胞死亡加剧。这些结果表明AATF是一种针对肾小管细胞氧化和凋亡损伤的新型细胞保护因子。AATF可能是IRI治疗应用的潜在候选物。