Department of Physiology & Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
J Cell Mol Med. 2011 May;15(5):1044-53. doi: 10.1111/j.1582-4934.2010.01221.x.
Apoptosis repressor with caspase recruitment domain (ARC) is a highly potent and multifunctional inhibitor of apoptosis that is physiologically expressed predominantly in post-mitotic cells such as cardiomyocytes, skeletal muscle cells and neurons. ARC was also found to be up-regulated in many forms of malignant tumours. ARC impairs the cellular apoptotic responsiveness to a wide range of stresses and insults, including extrinsic apoptosis initiation via death receptor ligands, dysregulation of cellular Ca(2+) homeostasis and endoplasmatic reticulum (ER) stress, genotoxic drugs, ionizing radiation, oxidative stress and hypoxia. ARC is subject to both transcriptional and post-translational regulation and exhibits its function through a multitude of molecular interactions with upstream transducers of apoptosis signals. This review summarizes, structures and comments on the published knowledge regarding ARC and its roles in modulating apoptotic cell death responsiveness in physiological and pathophysiological contexts.
凋亡抑制因子 with caspase recruitment domain (ARC) 是一种高效且多功能的凋亡抑制剂,主要在有丝分裂后细胞(如心肌细胞、骨骼肌细胞和神经元)中生理性表达。ARC 还在许多形式的恶性肿瘤中被发现上调。ARC 损害细胞对多种应激和损伤的凋亡反应性,包括通过死亡受体配体引发的外在凋亡起始、细胞内 Ca(2+) 稳态和内质网 (ER) 应激、遗传毒性药物、电离辐射、氧化应激和缺氧。ARC 受到转录和翻译后调控,并通过与凋亡信号的上游转导子的多种分子相互作用来发挥其功能。本综述总结、结构和评论了关于 ARC 的已发表知识及其在调节生理和病理生理环境中凋亡细胞死亡反应性中的作用。