Cook D I, Dinudom A, Komwatana P, Young J A
Dept. Physiology, University of Sydney, NSW, Australia.
Eur J Morphol. 1998 Aug;36 Suppl:67-73.
The duct cells of the mandibular glands of mice (and many other mammalian salivary glands) absorb NaCl from an isotonic, Na+-rich primary saliva, formed by the gland's secretory endpieces, utilising an amiloride-sensitive Na+ channel in the apical (luminal) domain of the plasma membranes. The present study focuses on the mechanisms whereby the apical membrane Na+ conductance is controlled so that the rate of Na+ influx from lumen to cytosol via the Na+ channels is matched to the rate of Na+ extrusion from cytosol to interstitium via the basolateral Na+-K+-ATPase (so called homocellular regulation or epithelial cross-talk). Our results show that the apical membrane Na+ conductance is not controlled by a sensor of extracellular (luminal) Na+, as has been previously believed, but by sensors of cytosolic Na+ and Cl- which down-regulate the Na+ channels when the cytosolic concentration of either ion increases. These effects of cytosolic Na+ and Cl- are mediated, respectively, by G proteins of the Gi and Go subclasses.
小鼠下颌腺(以及许多其他哺乳动物唾液腺)的导管细胞从由腺体分泌末端形成的等渗、富含Na⁺的初级唾液中吸收NaCl,这一过程利用了质膜顶端(管腔)区域的一种对氨氯吡脒敏感的Na⁺通道。本研究聚焦于顶端膜Na⁺电导的调控机制,以便通过Na⁺通道从管腔到细胞质的Na⁺内流速率与通过基底外侧Na⁺-K⁺-ATP酶从细胞质到间质的Na⁺外排速率相匹配(即所谓的同细胞调节或上皮细胞间通讯)。我们的结果表明,顶端膜Na⁺电导并非如先前认为的那样受细胞外(管腔)Na⁺传感器控制,而是受细胞质Na⁺和Cl⁻传感器控制,当这两种离子中任何一种的细胞质浓度升高时,它们会下调Na⁺通道。细胞质Na⁺和Cl⁻的这些作用分别由Gi和Go亚类的G蛋白介导。