Development of membrane ion channels during neural differentiation from human embryonic stem cells

被引:19
作者
Mirsadeghi, Sara [1 ]
Shahbazi, Ebrahim [1 ]
Hemmesi, Katayoun [1 ]
Nemati, Shiva [1 ]
Baharvand, Hossein [1 ,2 ]
Mirnajafi-Zadeh, Javad [3 ]
Kiani, Sahar [1 ]
机构
[1] ACECR, Royan Inst Stem Cell Biol & Technol, Cell Sci Res Ctr, Dept Stem Cells & Dev Biol, Tehran, Iran
[2] Univ Sci & Culture, Dept Dev Biol, Tehran, Iran
[3] Tarbiat Modares Univ, Fac Med Sci, Dept Physiol, POB 14115-331, Tehran, Iran
关键词
Human embryonic stem cell; Neural differentiation; Ion channel; Patch clamp; ELECTROPHYSIOLOGICAL PROPERTIES; IN-VITRO;
D O I
10.1016/j.bbrc.2017.07.068
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Objective: For human embryonic stem cells (hESCs) to differentiate into neurons, enormous changes has to occur leading to trigger action potential and neurotransmitter release. We attempt to determine the changes in expression of voltage gated channels (VGCs) and their electrophysiological properties during neural differentiation. Materials and methods: The relative expressions of alpha-subunit of voltage gated potassium, sodium and calcium channels were characterized by qRT-PCR technique. Patch clamp recording was performed to characterize the electrophysiological properties of hESCs during their differentiation into neuron-like cells. Results: Relative expression of a -subunit of channels changed significantly. 4-AP and TEA sensitive outward currents were observed in all stages, although TEA sensitive currents were recorded once in rosette structure. Nifedipine and QX314 sensitive inward currents were recorded only in neuron-like cells. Conclusion: K+ currents were recorded in hESCs and rosette structure cells. Inward currents, sensitive to Nifedipine and QX314, were recorded in neuron-like cells. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:166 / 172
页数:7
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