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ClC-3表达下调通过抑制容积激活氯电流减少表皮干细胞迁移。

Down-Regulation of ClC-3 Expression Reduces Epidermal Stem Cell Migration by Inhibiting Volume-Activated Chloride Currents.

作者信息

Guo Rui, Pan Fuqiang, Tian Yanping, Li Hongli, Li Shirong, Cao Chuan

机构信息

Department of Plastic and Reconstructive Surgery, Southwestern Hospital, Third Military Medical University, Chongqing, 400038, China.

Department of Histology and Embryology, Third Military Medical University, Chongqing, 400038, China.

出版信息

J Membr Biol. 2016 Jun;249(3):281-92. doi: 10.1007/s00232-015-9867-9. Epub 2016 Jan 14.

Abstract

ClC-3, a member of the ClC chloride (Cl(-)) channel family, has recently been proposed as the primary Cl(-) channel involved in cell volume regulation. Changes in cell volume influence excitability, contraction, migration, pathogen-host interactions, cell proliferation, and cell death processes. In this study, expression and function of ClC-3 channels were investigated during epidermal stem cell (ESC) migration. We observed differential expression of CLC-3 regulates migration of ESCs. Further, whole-cell patch-clamp recordings and image analysis demonstrated ClC-3 expression affected volume-activated Cl(-) current (I Cl,Vol) within ESCs. Live cell imaging systems, designed to observe cellular responses to overexpression and suppression of ClC-3 in real time, indicated ClC-3 may regulate ESC migratory dynamics. We employed IMARIS software to analyze the velocity and distance of ESC migration in vitro to demonstrate the function of ClC-3 channel in ESCs. As our data suggest volume-activated Cl(-) channels play a vital role in migration of ESCs, which contribute to skin repair by migrating from neighboring unwounded epidermis infundibulum, hair follicle or sebaceous glands, ClC-3 may represent a new and valuable target for stem cell therapies.

摘要

ClC-3是ClC氯化物(Cl⁻)通道家族的成员,最近被认为是参与细胞体积调节的主要Cl⁻通道。细胞体积的变化会影响兴奋性、收缩、迁移、病原体与宿主的相互作用、细胞增殖和细胞死亡过程。在本研究中,我们研究了表皮干细胞(ESC)迁移过程中ClC-3通道的表达和功能。我们观察到CLC-3的差异表达调节了ESC的迁移。此外,全细胞膜片钳记录和图像分析表明,ClC-3的表达影响了ESC内的体积激活Cl⁻电流(I Cl,Vol)。旨在实时观察细胞对ClC-3过表达和抑制反应的活细胞成像系统表明,ClC-3可能调节ESC的迁移动力学。我们使用IMARIS软件分析了体外ESC迁移的速度和距离,以证明ClC-3通道在ESC中的功能。由于我们的数据表明体积激活的Cl⁻通道在ESC迁移中起着至关重要的作用,ESC通过从邻近未受伤的表皮漏斗、毛囊或皮脂腺迁移来促进皮肤修复,因此ClC-3可能代表了干细胞治疗的一个新的有价值的靶点。

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