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TRPC3 is required for the survival, pluripotency and neural differentiation of mouse embryonic stem cells(mESCs) 被引量:5
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作者 Helen Baixia Hao Sarah E. Webb +3 位作者 Jianbo Yue Marc Moreau Catherine Leclerc Andrew L. Miller 《Science China(Life Sciences)》 SCIE CAS CSCD 2018年第3期253-265,共13页
Transient receptor potential canonical subfamily member 3(TRPC3) is known to be important for neural development and the formation of neuronal networks. Here, we investigated the role of TRPC3 in undifferentiated mous... Transient receptor potential canonical subfamily member 3(TRPC3) is known to be important for neural development and the formation of neuronal networks. Here, we investigated the role of TRPC3 in undifferentiated mouse embryonic stem cells(mESCs) and during the differentiation of mESCs into neurons. CRISPR/Cas9-mediated knockout(KO) of TRPC3 induced apoptosis and the disruption of mitochondrial membrane potential both in undifferentiated mESCs and in those undergoing neural differentiation. In addition, TRPC3 KO impaired the pluripotency of mESCs. TRPC3 KO also dramatically repressed the neural differentiation of mESCs by inhibiting the expression of markers for neural progenitors, neurons, astrocytes and oligodendrocytes.Taken together, our new data demonstrate an important function of TRPC3 with regards to the survival, pluripotency and neural differentiation of mESCs. 展开更多
关键词 transient receptor potential canonical subfamily member 3 (TRPC3 mouse embryonic stem cells (mESCs) neurondifferentiation CRISPR/Cas9 PLURIPOTENCY APOPTOSIS mitochondrial membrane potential
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