{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T17:31:28Z","timestamp":1792171888590,"version":"4.4.0"},"reference-count":56,"publisher":"American Physiological Society","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American Journal of Physiology-Gastrointestinal and Liver Physiology"],"published-print":{"date-parts":[[2004,2]]},"abstract":"<jats:p>Large volumes of saliva are generated by transepithelial Cl<jats:sup>-<\/jats:sup>movement during parasympathetic muscarinic receptor stimulation. To gain further insight into a major Cl<jats:sup>-<\/jats:sup>uptake mechanism involved in this process, we have characterized the anion exchanger (AE) activity in mouse serous parotid and mucous sublingual salivary gland acinar cells. The AE activity in acinar cells was Na<jats:sup>+<\/jats:sup>independent, electroneutral, and sensitive to the anion exchange inhibitor DIDS, properties consistent with the AE members of the SLC4A gene family. Localization studies using a specific antibody to the ubiquitously expressed AE2 isoform labeled acini in both parotid and sublingual glands. Western blot analysis detected an \u223c170-kDa protein that was more highly expressed in the plasma membranes of sublingual than in parotid glands. Correspondingly, the DIDS-sensitive [Formula: see text] exchanger activity was significantly greater in sublingual acinar cells. The carbonic anhydrase antagonist acetazolamide markedly inhibited, whereas muscarinic receptor stimulation enhanced, the [Formula: see text] exchanger activity in acinar cells from both glands. Intracellular Ca<jats:sup>2+<\/jats:sup>chelation prevented muscarinic receptor-induced upregulation of the AE, whereas raising the intracellular Ca<jats:sup>2+<\/jats:sup>concentration with the Ca<jats:sup>2+<\/jats:sup>-ATPase inhibitor thapsigargin mimicked the effects of muscarinic receptor stimulation. In summary, carbonic anhydrase activity was essential for regulating [Formula: see text] exchange in salivary gland acinar cells. Moreover, muscarinic receptor stimulation enhanced AE activity through a Ca<jats:sup>2+<\/jats:sup>-dependent mechanism. Such forms of regulation may play important roles in modulating fluid and electrolyte secretion by salivary gland acinar cells.<\/jats:p>","DOI":"10.1152\/ajpgi.00158.2003","type":"journal-article","created":{"date-parts":[[2004,1,31]],"date-time":"2004-01-31T01:09:44Z","timestamp":1075511384000},"page":"G312-G320","source":"Crossref","is-referenced-by-count":45,"title":["Cl<sup>-<\/sup>\/HCO<sub>3<\/sub><sup>-<\/sup>exchange is acetazolamide sensitive and activated by a muscarinic receptor-induced [Ca<sup>2+<\/sup>]<sub>i<\/sub>increase in salivary acinar cells"],"prefix":"10.1152","volume":"286","author":[{"given":"Ha-Van","family":"Nguyen","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alan","family":"Stuart-Tilley","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Seth 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