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Am J Physiol Cell Physiol 274: C1017-C1029, 1998;
0363-6143/98 $5.00
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Vol. 274, Issue 4, C1017-C1029, April 1998

Identification of clathrin and clathrin adaptors on tubulovesicles of gastric acid secretory (oxyntic) cells

Curtis T. Okamoto1, Sherif M. Karam2, Young Y. Jeng1, John G. Forte2, and James R. Goldenring3

1 Department of Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles 90033; 2 Department of Molecular and Cell Biology, University of California, Berkeley, California 94720; and 3 Institute for Molecular Medicine and Genetics, Medical College of Georgia, Augusta, Georgia 30912-3175

gamma -Adaptin and clathrin heavy chain were identified on tubulovesicles of gastric oxyntic cells with the anti-gamma -adaptin monoclonal antibody (MAb) 100/3 and an anti-clathrin heavy chain MAb (MAb 23), respectively. In Western blots, crude gastric microsomes from rabbit and rat and density gradient-purified, H-K-ATPase-rich microsomes from these same species were immunoreactive for gamma -adaptin and clathrin. In immunofluorescent labeling of isolated rabbit gastric glands, anti-gamma -adaptin and anti-clathrin heavy chain immunoreactivity appeared to be concentrated in oxyntic cells. In primary cultures of rabbit oxyntic cells, the immunocytochemical distribution of gamma -adaptin immunoreactivity was similar to that of the tubulovesicular membrane marker in oxyntic cells, the H-K-ATPase. Further biochemical characterization of the tubulovesicular gamma -adaptin-containing complex suggested that it has a subunit composition that is typical of that for a clathrin adaptor: in addition to the gamma -adaptin subunit, it contains a beta -adaptin subunit and other subunits of apparent molecular masses of 50 kDa and 19 kDa. From solubilized gastric microsomes from rabbit, gamma -adaptin could be copurified with the major cargo protein of tubulovesicles, the H-K-ATPase. Thus this tubulovesicular coat may bind directly to the H-K-ATPase and may thereby mediate the regulated trafficking of the H-K-ATPase at the apical membrane of the oxyntic cell during the gastric acid secretory cycle. Given the similarities of the regulated trafficking of the H-K-ATPase with recycling of cargo through the apical recycling endosome of many epithelial cells, we propose that tubulovesicular clathrin and adaptors may regulate some part of an apical recycling pathway in other epithelial cells.

hydrogen-potassium-adenosine 5'-triphosphatase trafficking; apical membrane recycling; internalization motif


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