文献类型：期刊文献

英文题名：DSTYK knockout affects the architecture of F-actin cytoskeleton in mouse renal proximal convoluted tubules

作者：Liu, Ji-Wei[1];Mao, Lin[2];Zhu, Zhi-Chuan[1];Li, Kui[1];Liao, Lu-Jian[2];Xiong, Zhi-Qi[1];Hu, Ze-Lan[1];Zheng, Jing[1]

机构：[1]East China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab New Drug Design, Shanghai 200237, Peoples R China;[2]East China Normal Univ, Sch Life Sci, Shanghai 200062, Peoples R China

年份：2017

卷号：10

期号：5

起止页码：6157

外文期刊名：INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY

收录：;WOS:【SCI-EXPANDED(收录号:WOS:000402279600139)】；

基金：Financial supports from the National Natural Science Foundation of China (Grant number 31300904) and the International Postdoctoral Exchange Fellowship Program (No. 20130018) are acknowledged. We also thank professor Hui Yang for providing us with PX330-GFP plasmid.

语种：英文

外文关键词：DSTYK; CAKUT; F-actin; proximal convoluted tubules; Profilin 1; Profilin 2

摘要：Mutations of dual serine/threonine and tyrosine protein kinase (DSTYK) are linked to congenital anomalies of the kidney and urinary tract (CAKUT). However, the function of DSTYK in the normal kidney and its role in the pathogenesis of CAKUT remain largely unknown. In this study, we investigated the role of DSTYK in the kidney by analyzing the consequences of Dstyk ablation in mice. We found that DSTYK deficiency resulted in swelling and diffuse distribution of F-actin cytoskeleton in proximal convoluted tubules. However, the architecture of F-actin cytoskeleton in the descending thin limb of Henel's loop, the thick ascending limb of Henel's loop, distal convoluted tubules, connecting tubules, collecting ducts and glomeruli was not affected following DSTYK deletion. The appearance of the urogenital system and the gross kidney anatomy of Dstyk(-/-) mice were normal. Also, no significant difference in the renal corpuscle's diameter and the density of glomeruli was found between Dstyk(+/+) and Dstyk(-/-) mice. To identify DSTYK binding partners, we generated a Flag-DSTYK knockin HEK 293T cell line with Flag tag sequence inserted to the N-terminus of endogenous DSTYK gene using CRISPR/Cas9 system. A total list of 67 proteins were identified by Co-immunoprecipitation (Co-IP)/mass spectrometry (MS) that potentially interact with DSTYK, mostly enzymes (39.0%), nucleic acid binding proteins (36.6%) and cytoskeletal proteins (14.6%). Profilin 1 and Profilin 2 were validated as bona fide DSTYK binding partners by Co-IP assay. These results uncover a role of DSTYK in the regulation of F-actin cytoskeleton in the mouse renal proximal convoluted tubules.