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温暖的温度会激活小鼠308角质形成细胞中的TRPV4。

Warm temperatures activate TRPV4 in mouse 308 keratinocytes.

作者信息

Chung Man-Kyo, Lee Hyosang, Caterina Michael J

机构信息

Department of Biological Chemistry, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

J Biol Chem. 2003 Aug 22;278(34):32037-46. doi: 10.1074/jbc.M303251200. Epub 2003 Jun 3.

Abstract

Mammalian survival requires constant monitoring of environmental and body temperature. Recently, several members of the transient receptor potential vanilloid (TRPV) subfamily of ion channels have been identified that can be gated by increases in temperature into the warm (TRPV3 and TRPV4) or painfully hot (TRPV1 and TRPV2) range. In rodents, TRPV3 and TRPV4 proteins have not been detected in sensory neurons but are highly expressed in skin epidermal keratinocytes. Here, we show that in response to warm temperatures (>32 degrees C), the mouse 308 keratinocyte cell line exhibits nonselective transmembrane cationic currents and Ca2+ influx. Both TRPV3 and TRPV4 are expressed in 308 cells. However, the warmth-evoked responses we observe most closely resemble those mediated by recombinant TRPV4 on the basis of their electrophysiological properties and sensitivity to osmolarity and the phorbol ester, 4alpha-phorbol-12,13-didecanoate. Together, these data support the notion that keratinocytes are capable of detecting modest temperature elevations, strongly suggest that TRPV4 participates in these responses, and define a system for the cell biological analysis of warmth transduction.

摘要

哺乳动物的生存需要持续监测环境温度和体温。最近,已鉴定出离子通道瞬时受体电位香草酸亚家族(TRPV)的几个成员,它们可被温度升高激活,进入温暖(TRPV3和TRPV4)或疼痛的高温(TRPV1和TRPV2)范围。在啮齿动物中,尚未在感觉神经元中检测到TRPV3和TRPV4蛋白,但它们在皮肤表皮角质形成细胞中高度表达。在这里,我们表明,在温暖温度(>32摄氏度)刺激下,小鼠308角质形成细胞系表现出非选择性跨膜阳离子电流和Ca2+内流。TRPV3和TRPV4均在308细胞中表达。然而,基于其电生理特性以及对渗透压和佛波酯4α-佛波醇-12,13-十二烷酸酯的敏感性,我们观察到的温热诱发反应与重组TRPV4介导的反应最为相似。这些数据共同支持角质形成细胞能够检测适度温度升高的观点,强烈表明TRPV4参与了这些反应,并定义了一个用于温热转导细胞生物学分析的系统。

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