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Am J Physiol Gastrointest Liver Physiol 287: G253-G263, 2004. First published February 19, 2004; doi:10.1152/ajpgi.00033.2004
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HORMONES AND SIGNALING

Secretagogue-induced translocation of CRHSP-28 within an early apical endosomal compartment in acinar cells

Diana D. H. Thomas, Ning Weng, and Guy E. Groblewski

Department of Nutritional Sciences, University of Wisconsin, Madison, Wisconsin 53706

Submitted 20 January 2004 ; accepted in final form 19 February 2004

Ca2+-regulated heat-stable protein (CRHSP-28) is a member of the TPD52 protein family that has been shown to regulate Ca2+-dependent secretory activity in pancreatic acinar cells. Immunofluorescence microscopy of isolated lobules demonstrated that CRHSP-28 is localized to a supranuclear apical compartment in acini and accumulates immediately below the apical membrane within 2 min of CCK octapeptide (CCK-8) stimulation. Dual-immunofluorescence microscopy demonstrated an endosomal localization of CRHSP-28 that strongly overlapped with early endosomal antigen-1 (EEA-1) on vesicular structures throughout the apical cytoplasm but showed only minimal overlap with the transferrin receptor, which is present in basolaterally derived endosomes. Significant overlapping of CRHSP-28 with the trans-Golgi network marker-38 was also noted in supranuclear regions of acini. Interestingly, treatment of lobules with brefeldin A reversibly disrupted the vesicular localization of CRHSP-28 and EEA-1 within the apical cytoplasm. The CCK-8-induced accumulation of CRHSP-28 in subapical regions of acini was not altered by inhibition of apical endocytosis with the actin filament-disrupting agent latrunculin B. Immunoelectron microscopy confirmed that CRHSP-28 is associated with the limiting membrane of irregularly shaped vesicular structures of low electron density in the apical cytoplasm that are positive for EEA-1 staining. Sparse, but significant, CRHSP-28 immunoreactivity was also observed along the limiting membrane of zymogen granules. Consistent with immunofluorescence data, CRHSP-28 was found to accumulate in clusters on endosomes and positioned between zymogen granules below the cell apex on CCK-8 stimulation. These data indicate that CRHSP-28 is present within endocytic and exocytic compartments of acinar cells and is acutely regulated by secretagogue stimulation.

calcium signaling; membrane trafficking; early endosome; secretion; calcium/calmodulin-dependent protein kinase II



Address for reprint requests and other correspondence: G. E. Groblewski, Dept. of Nutritional Sciences, Univ. of Wisconsin, 1415 Linden Dr., Madison, WI 53706 (E-mail: groby{at}nutrisci.wisc.edu).




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