Turner J T, Weisman G A, Landon L A, Park M, Camden J M
Dept. Pharmacology, School of Medicine, University of Missouri-Columbia, 65212, USA.
Eur J Morphol. 1998 Aug;36 Suppl:170-5.
A growing body of information now supports the suggestion that P2 receptors for extracellular nucleotides (primarily ATP) have a role in regulating salivary gland function. There is solid pharmacological and molecular evidence for the presence of P2X ligand-gated ion channel nucleotide receptors (P2X4 and P2X7/P2Z). More recently, our group and others have obtained evidence that multiple P2Y G protein-coupled nucleotide receptors (P2Y1 and P2Y2) are also expressed. Our studies have focused on defining the conditions under which P2Y receptors are expressed, the functional consequences of their activation, and the importance of co-expression of P2X and P2Y receptors. Functional and molecular approaches have been used to identify the P2 subtypes in salivary glands and in salivary cell lines. Assays include measurement of changes in [Ca2+]i, changes in transcellular short circuit current in monolayers, and RT-PCR to assess changes in receptor mRNA levels. The main observations are: (1) P2Y1 receptor activity is present in the submandibular gland (SMG) of immature rats but decreases over the first four weeks following birth, although mRNA levels remain relatively constant; (2) P2Y2 receptors are present in the cell lines and are up-regulated during short-term culture of normal parotid, sublingual, and SMG cells and following ligation of the main excretory duct of SMG; and (3) the P2X subtypes, P2X4 and P2X7, and the P2Y subtypes, P2Y1 and P2Y2, are co-expressed in salivary glands and salivary cell lines, and exhibit distinct basolateral versus apical localization in polarized cell monolayers as well as discrete patterns of intracellular signaling.
越来越多的信息支持这样一种观点,即细胞外核苷酸(主要是ATP)的P2受体在调节唾液腺功能中起作用。有确凿的药理学和分子证据表明存在P2X配体门控离子通道核苷酸受体(P2X4和P2X7/P2Z)。最近,我们小组和其他研究小组已获得证据,表明还表达了多种P2Y G蛋白偶联核苷酸受体(P2Y1和P2Y2)。我们的研究集中在确定P2Y受体表达的条件、其激活的功能后果以及P2X和P2Y受体共表达的重要性。已使用功能和分子方法来鉴定唾液腺和唾液细胞系中的P2亚型。检测方法包括测量[Ca2+]i的变化、单层细胞跨细胞短路电流的变化以及用于评估受体mRNA水平变化的RT-PCR。主要观察结果如下:(1)P2Y1受体活性存在于未成熟大鼠的下颌下腺(SMG)中,但在出生后的头四周内降低,尽管mRNA水平保持相对恒定;(2)P2Y2受体存在于细胞系中,并且在正常腮腺、舌下腺和SMG细胞的短期培养期间以及SMG主排泄管结扎后上调;(3)P2X亚型P2X4和P2X7以及P2Y亚型P2Y1和P2Y2在唾液腺和唾液细胞系中共表达,并且在极化细胞单层中表现出不同的基底外侧与顶端定位以及离散的细胞内信号传导模式。