CRHSP-28 Regulates Ca2+-stimulated Secretion in Permeabilized Acinar Cells
CRHSP-28 is a Ca 2+ -regulated heat-stable phosphoprotein, abundant in the apical cytoplasm of epithelial cells that are specialized in exocrine protein secretion. To define a functional role for the protein in pancreatic secretion, recombinant CRHSP-28 (rCRHSP-28) was introduced into streptolysin-O...
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Veröffentlicht in: | The Journal of biological chemistry 2001-08, Vol.276 (31), p.28866-28872 |
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Sprache: | eng |
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Zusammenfassung: | CRHSP-28 is a Ca 2+ -regulated heat-stable phosphoprotein, abundant in the apical cytoplasm of epithelial cells that are specialized in exocrine
protein secretion. To define a functional role for the protein in pancreatic secretion, recombinant CRHSP-28 (rCRHSP-28) was
introduced into streptolysin-O-permeabilized acinar cells, and amylase secretion in response to elevated Ca 2+ was determined. Secretion was enhanced markedly by rCRHSP-28 over a time course that closely corresponded with the loss of
the native protein from the intracellular compartment. No effects of rCRHSP-28 were detected until â¼50% of the native protein
was lost from the cytosol. Secretion was enhanced by rCRHSP-28 over a physiological range of Ca 2+ concentrations with 2â3-fold increases in amylase release occurring in response to low micromolar levels of free Ca 2+ . Further, rCRHSP-28 augmented secretion in a concentration-dependent manner with minimal and maximal effects occurring at
1 and 25 μg/ml, respectively. Covalent cross-linking experiments demonstrated that native CRHSP-28 was present in a 60-kDa
complex in cytosolic fractions and in a high molecular mass complex in particulate fractions, consistent with the slow leak
rate of the protein from streptolysin-O-permeabilized cells. Probing acinar lysates with rCRHSP-28 in a gel-overlay assay
identified two CRHSP-28-binding proteins of 35 (pp35) and 70 kDa (pp70). Interestingly, preparation of lysates in the presence
of 1 m m Ca 2+ resulted in a marked redistribution of both proteins from a cytosolic to a Triton X-100-insoluble fraction, suggesting a
Ca 2+ -sensitive interaction of these proteins with the acinar cell cytoskeleton. In agreement with our previous study immunohistochemically
localizing CRHSP-28 around secretory granules in acinar cells, gel-overlay analysis revealed pp70 copurified with acinar cell
secretory granule membranes. These findings demonstrate an important cell physiological function for CRHSP-28 in the Ca 2+ -regulated secretory pathway of acinar cells. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M102214200 |