SALIVARY-GLAND NUCLEOTIDE RECEPTORS - EVIDENCE FOR FUNCTIONAL EXPRESSION OF BOTH P2X AND P2Y SUBTYPES

Citation
Jt. Turner et al., SALIVARY-GLAND NUCLEOTIDE RECEPTORS - EVIDENCE FOR FUNCTIONAL EXPRESSION OF BOTH P2X AND P2Y SUBTYPES, European journal of morphology, 36, 1998, pp. 170-175
Citations number
23
Categorie Soggetti
Anatomy & Morphology
ISSN journal
09243860
Volume
36
Year of publication
1998
Supplement
S
Pages
170 - 175
Database
ISI
SICI code
0924-3860(1998)36:<170:SNR-EF>2.0.ZU;2-2
Abstract
A growing body of information now supports the suggestion that P2 rece ptors for extracellular nucleotides (primarily ATP) have a role in reg ulating salivary gland function. There is solid pharmacological and mo lecular evidence for the presence of P2X ligand-gated ion channel nucl eotide receptors (P2X(4) and P2X(7)/P-2Z). More recently, our group an d others have obtained evidence that multiple P2Y G protein-coupled nu cleotide receptors (P2Y(1) and P2Y(2)) 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 i mportance of co-expression of P2X and P2Y receptors. Functional and mo lecular approaches have been used to identify the P2 subtypes in saliv ary glands and in salivary cell lines. Assays include measurement of c hanges 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) P2Y(1) receptor activity is present in the submandibular gland (SMG) of immature rats but decreases over the fir st four weeks following birth, although mRNA levels remain relatively constant, (2) P2Y(2) receptors are present in the cell lines and are u pregulated during short-term culture of normal parotid, sublingual, an d SMG cells and following ligation of the main excretory duct of SMG; and (3) the P2X subtypes, P2X(4) and P2X(7), and the P2Y subtypes, P2Y (1) and P2Y(2), are coexpressed in salivary glands and salivary cell l ines, and exhibit distinct basolateral versus apical localization in p olarized cell monolayers as well as discrete patterns of intracellular signaling.