Shimizu Taiki, Uchida Chiyoko, Shimizu Ritsuko, Motohashi Hozumi, Uchida Takafumi
Molecular Enzymology, Department of Molecular Cell Science, Tohoku University, 468-1 Aoba, Aramaki, Aoba, Sendai, Miyagi 980-0845, Japan.
Department of Human Development and Culture, Fukushima University, 1 Kanayagawa, Fukushima, Fukushima 960-1296, Japan.
Biochem Biophys Res Commun. 2017 Nov 18;493(2):946-951. doi: 10.1016/j.bbrc.2017.09.115. Epub 2017 Sep 21.
Here we show that Pin1, a peptidyl-prolyl cis/trans isomerase which catalyzes the isomerization of phosphorylated Ser/Thr-Pro, is a regulatory molecule of thrombopoiesis. We found that mice lacking the Pin1 gene (Pin1 mice) formed more megakaryocytes (MKs) than wild type mice (WT mice), and that the proplatelet formation of MKs was poorer in Pin1 mice than WT mice. Treatment of Meg-01 cells, a megakaryoblastic floating cell line, with shRNA against Pin1 suppressed the proplatelet formation. Expression of tau, a microtubule associated protein was induced in MKs during proplatelet formation. Pin1 bound tau and promoted microtubule polymerization. Our results show that Pin1 serves as a positive regulatory molecule of proplatelet formation of MKs by enhancing the function of phosphorylated tau.
我们在此表明,Pin1是一种肽基脯氨酰顺/反异构酶,可催化磷酸化的丝氨酸/苏氨酸-脯氨酸的异构化,它是血小板生成的调节分子。我们发现,缺乏Pin1基因的小鼠(Pin1小鼠)比野生型小鼠(WT小鼠)形成更多的巨核细胞(MKs),并且Pin1小鼠中MKs的前血小板形成比WT小鼠差。用针对Pin1的短发夹RNA(shRNA)处理巨核母细胞漂浮细胞系Meg-01细胞可抑制前血小板形成。在血小板生成过程中,微管相关蛋白tau在MKs中被诱导表达。Pin1与tau结合并促进微管聚合。我们的结果表明,Pin1通过增强磷酸化tau的功能,作为MKs前血小板形成的正调节分子。