Nucleosome Assembly Protein 1-Like 1 (Nap1l1) Regulates the Proliferation of Murine Induced Pluripotent Stem Cells

被引:19
|
作者
Yan, Yuan [1 ,2 ,3 ]
Yin, Peipei [1 ,2 ]
Gong, Hui [1 ,2 ]
Xue, Yuanyuan [1 ,2 ]
Zhang, Guoping [1 ,2 ]
Fang, Bo [1 ,2 ]
Chen, Zhidan [1 ,2 ]
Li, Yang [1 ,2 ]
Yang, Chunjie [1 ,2 ]
Huang, Zheyong [1 ,2 ]
Yang, Xiangdong [1 ,2 ]
Ge, Junbo [1 ,2 ]
Zou, Yunzeng [1 ,2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Shanghai Inst Cardiovasc Dis, 180 Feng Lin Rd, Shanghai 200032, Peoples R China
[2] Fudan Univ, Inst Biomed Sci, 180 Feng Lin Rd, Shanghai 200032, Peoples R China
[3] Southern Med Univ, Coll Basic Med, Dept Histol & Embryol, Guangzhou, Guangdong, Peoples R China
关键词
Nap1l1; iPS; Proliferation; Apoptosis; Cell cycle; HISTONE CHAPERONES; DIFFERENTIATION; APOPTOSIS; KINASE; GROWTH; INHIBITOR; CYCLINS; GENE; P21; P53;
D O I
10.1159/000438634
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: To investigate whether nucleosome assembly protein 1-like 1 (Nap1l1) regulates the proliferation of induced pluripotent stem cells (iPSC) and the potential mechanisms. Methods: Nap1l1-knockdown-iPSC and Nap1l1-overexpression-iPSC were constructed by transfection of lentiviral particles. The proliferation of iPSC was detected by MTT analysis, and cell cycle was analyzed by flow cytometry. Results: Nap1l1 overexpression promoted iPSC proliferation and induced G2/M transition compared to their control iPSC while Nap1l1-knockdown-iPSC dramatically displayed the reduced proliferation and accumulated G2/M phase cells. Further analysis showed that Nap1l1 overexpression in iPSC increased the expression of cyclin B1, downregulated the expression of p21 and p27, while knockdown of Nap1l1 showed the opposite effects. In addition, overexpression of Nap1l1 promoted the phosphorylation of AKT and ERK in iPSC, while knockdown of Nap1l1 inhibited the effects. However, these effects displayed in Nap1l1-overexpression-iPSC were greatly suppressed by the inhibition of AKT or ERK signaling. Conclusions: The results indicate that Nap1l1 promotes the proliferation of iPSC attributable to G2/M transition caused by downregulation of p27 and p21, and upregulation of cyclin B1, the activation of AKT or ERK is involved in the process. The present study has revealed a novel molecular mechanism involved in the proliferation of iPSC. (C) 2016 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:340 / 350
页数:11
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