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来自水通道蛋白5缺陷小鼠的唾液腺泡细胞的膜水通透性降低,且细胞体积调节发生改变。

Salivary acinar cells from aquaporin 5-deficient mice have decreased membrane water permeability and altered cell volume regulation.

作者信息

Krane C M, Melvin J E, Nguyen H V, Richardson L, Towne J E, Doetschman T, Menon A G

机构信息

Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267-0524, USA.

出版信息

J Biol Chem. 2001 Jun 29;276(26):23413-20. doi: 10.1074/jbc.M008760200. Epub 2001 Apr 4.

DOI:10.1074/jbc.M008760200
PMID:11290736
Abstract

Aquaporins (AQPs) are channel proteins that regulate the movement of water through the plasma membrane of secretory and absorptive cells in response to osmotic gradients. In the salivary gland, AQP5 is the major aquaporin expressed on the apical membrane of acinar cells. Previous studies have shown that the volume of saliva secreted by AQP5-deficient mice is decreased, indicating a role for AQP5 in saliva secretion; however, the mechanism by which AQP5 regulates water transport in salivary acinar cells remains to be determined. Here we show that the decreased salivary flow rate and increased tonicity of the saliva secreted by Aqp5(-)/- mice in response to pilocarpine stimulation are not caused by changes in whole body fluid homeostasis, indicated by similar blood gas and electrolyte concentrations in urine and blood in wild-type and AQP5-deficient mice. In contrast, the water permeability in parotid and sublingual acinar cells isolated from Aqp5(-)/- mice is decreased significantly. Water permeability decreased by 65% in parotid and 77% in sublingual acinar cells from Aqp5(-)/- mice in response to hypertonicity-induced cell shrinkage and hypotonicity-induced cell swelling. These data show that AQP5 is the major pathway for regulating the water permeability in acinar cells, a critical property of the plasma membrane which determines the flow rate and ionic composition of secreted saliva.

摘要

水通道蛋白(AQPs)是一种通道蛋白,可响应渗透梯度调节水通过分泌细胞和吸收细胞的质膜的运动。在唾液腺中,AQP5是在腺泡细胞顶端膜上表达的主要水通道蛋白。先前的研究表明,AQP5缺陷型小鼠分泌的唾液量减少,这表明AQP5在唾液分泌中起作用;然而,AQP5调节唾液腺泡细胞中水运输的机制仍有待确定。在这里,我们表明,Aqp5(-)/-小鼠在毛果芸香碱刺激下唾液流速降低和唾液渗透压升高,并非由全身液体稳态的变化引起,野生型和AQP5缺陷型小鼠尿液和血液中的血气和电解质浓度相似表明了这一点。相反,从Aqp5(-)/-小鼠分离的腮腺和舌下腺泡细胞的水通透性显著降低。响应高渗诱导的细胞收缩和低渗诱导的细胞肿胀,Aqp5(-)/-小鼠腮腺腺泡细胞的水通透性降低了65%,舌下腺泡细胞降低了77%。这些数据表明,AQP5是调节腺泡细胞水通透性的主要途径,这是质膜的一个关键特性,决定了分泌唾液的流速和离子组成。

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Salivary acinar cells from aquaporin 5-deficient mice have decreased membrane water permeability and altered cell volume regulation.来自水通道蛋白5缺陷小鼠的唾液腺泡细胞的膜水通透性降低,且细胞体积调节发生改变。
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