Department of Nephrology, The Children Hospital of Zhejiang University School of Medicine, #57 Zhugan Lane, Hangzhou, 310003, Zhejiang Province, People's Republic of China.
Chronic Disease Research Institute, Department of Nutrition and Food Hygiene, Zhejiang University School of Public Health, Hangzhou, 310058, Zhejiang Province, People's Republic of China.
Cell Commun Signal. 2019 Aug 6;17(1):91. doi: 10.1186/s12964-019-0402-y.
Protein phosphorylation & dephosphorylation are ubiquitous cellular processes that allow for the nuanced and reversible regulation of protein activity. Protein phosphatase 2A (PP2A) is a multifunction phosphatase that is well expressed in all cell types of kidney during early renal development, though its functions in kidney remains to be elucidated.
PP2A conditional knock-out mice was generated with PP2A fl/fl mice that were crossed with Podocin-Cre mice. The phenotype of Pod-PP2A-KO mice (homozygous for the floxed PP2A allele with Podocin-Cre) and littermate PP2A fl/fl controls (homozygous for the PP2A allele but lacking Podocin-Cre) were further studied. Primary podocytes isolated from the Pod-PP2A-KO mice were cultured and they were then employed with sing label-free nano-LC - MS/MS technology on a Q-exactive followed by SIEVE processing to identify possible target molecular entities for the dephosphorylation effect of PP2A, in which Western blot and immunofluorescent staining were used to analyze further.
Pod-PP2A-KO mice were developed with weight loss, growth retardation, proteinuria, glomerulopathy and foot process effacement, together with reduced expression of some slit diaphragm molecules and cytoskeleton rearrangement of podocytes. Y box protein 1 (YB-1) was identified to be the target molecule for dephosphorylation effect of PP2A. Furthermore, YB-1 phosphorylation was up-regulated in the Pod-PP2A-KO mice in contrast to the wild type controls, while total and un-phosphorylated YB-1 both was moderately down-regulated in podocytes from the Pod-PP2A-KO mice.
Our study revealed the important role of PP2A in regulating the development of foot processes and fully differentiated podocytes whereas fine-tuning of YB-1 via a post-translational modification by PP2A regulating its activity might be crucial for the functional integrity of podocytes and glomerular filtration barrier.
蛋白质磷酸化和去磷酸化是普遍存在的细胞过程,允许对蛋白质活性进行细致和可逆的调节。蛋白磷酸酶 2A(PP2A)是一种多功能磷酸酶,在早期肾发育过程中,肾脏的所有细胞类型中均有良好表达,但其在肾脏中的功能尚待阐明。
利用 PP2A fl/fl 小鼠与 Podocin-Cre 小鼠杂交,生成 PP2A 条件性敲除小鼠。进一步研究 Pod-PP2A-KO 小鼠(杂合子 floxed PP2A 等位基因与 Podocin-Cre)和同窝对照 PP2A fl/fl 小鼠(杂合子 PP2A 等位基因但缺乏 Podocin-Cre)的表型。从 Pod-PP2A-KO 小鼠中分离出原代足细胞进行培养,然后采用单标记无标记纳升 LC-MS/MS 技术在 Q-exactive 上进行分析,随后进行 SIEVE 处理,以鉴定 PP2A 去磷酸化作用的可能靶分子实体,其中采用 Western blot 和免疫荧光染色进行进一步分析。
成功构建了 Pod-PP2A-KO 小鼠,表现为体重减轻、生长迟缓、蛋白尿、肾小球病变和足突融合,同时一些裂孔隔膜分子的表达减少和足细胞骨架重排。鉴定出 Y 盒蛋白 1(YB-1)是 PP2A 去磷酸化作用的靶分子。此外,与野生型对照相比,Pod-PP2A-KO 小鼠中的 YB-1 磷酸化水平上调,而 Pod-PP2A-KO 小鼠足细胞中的总 YB-1 和未磷酸化 YB-1 均适度下调。
本研究揭示了 PP2A 在调节足突发育和完全分化的足细胞中的重要作用,通过 PP2A 调节其活性的翻译后修饰精细调节 YB-1 可能对足细胞和肾小球滤过屏障的功能完整性至关重要。