Hays Thomas, Ma'ayan Avi, Clark Neil R, Tan Christopher M, Teixeira Avelino, Teixeira Angela, Choi Jae W, Burdis Nora, Jung Sung Yun, Bajaj Amol O, O'Malley Bert W, He John C, Hyink Deborah P, Klotman Paul E
Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, United States of Americ.
Department of Pharmacology and Systems Therapeutics, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America.
PLoS One. 2014 Jun 20;9(6):e100660. doi: 10.1371/journal.pone.0100660. eCollection 2014.
MYH9 encodes non-muscle myosin heavy chain IIA (NMMHCIIA), the predominant force-generating ATPase in non-muscle cells. Several lines of evidence implicate a role for MYH9 in podocytopathies. However, NMMHCIIA's function in podocytes remains unknown. To better understand this function, we performed immuno-precipitation followed by mass-spectrometry proteomics to identify proteins interacting with the NMMHCIIA-enriched actin-myosin complexes. Computational analyses revealed that these proteins belong to functional networks including regulators of cytoskeletal organization, metabolism and networks regulated by the HIV-1 gene nef. We further characterized the subcellular localization of NMMHCIIA within podocytes in vivo, and found it to be present within the podocyte major foot processes. Finally, we tested the effect of loss of MYH9 expression in podocytes in vitro, and found that it was necessary for cytoskeletal organization. Our results provide the first survey of NMMHCIIA-enriched actin-myosin-interacting proteins within the podocyte, demonstrating the important role of NMMHCIIA in organizing the elaborate cytoskeleton structure of podocytes. Our characterization of NMMHCIIA's functions goes beyond the podocyte, providing important insights into its general molecular role.
MYH9编码非肌肉肌球蛋白重链IIA(NMMHCIIA),它是非肌肉细胞中主要的产生力的ATP酶。有几条证据表明MYH9在足细胞病变中起作用。然而,NMMHCIIA在足细胞中的功能仍然未知。为了更好地理解这一功能,我们进行了免疫沉淀,随后进行质谱蛋白质组学分析,以鉴定与富含NMMHCIIA的肌动蛋白-肌球蛋白复合物相互作用的蛋白质。计算分析表明,这些蛋白质属于功能网络,包括细胞骨架组织调节因子、代谢以及受HIV-1基因nef调节的网络。我们进一步在体内对足细胞中NMMHCIIA的亚细胞定位进行了表征,发现它存在于足细胞主要足突内。最后,我们在体外测试了足细胞中MYH9表达缺失的影响,发现它对细胞骨架组织是必需的。我们的结果首次对足细胞内富含NMMHCIIA的肌动蛋白-肌球蛋白相互作用蛋白进行了研究,证明了NMMHCIIA在组织足细胞精细的细胞骨架结构中的重要作用。我们对NMMHCIIA功能的表征超出了足细胞的范围,为其一般分子作用提供了重要见解。