Abstract
A partially purified secretory granule fraction, isolated from rat islets of Langerhans by differential centrifugation, was used for investigating the stability of the beta granules during incubation in various conditions. Effects of pH, temperature, and time were studied; the granules possessed optimal stability at 4 degrees and pH 6.0, and could be solubilized at pH 4.0 or 8.5, or in the presence of sodium deoxycholate, but not by phospholipase c, ouabain, or alloxan. Incubation with glucose or some of its metabolites, or with tolbutamide, ATP, or cyclic 3',5'-AMP did not alter the stability of the beta granules Exogenous insulin-(131)I was not bound by the isolated granules under the conditions used; no specific insulin-degrading activity could be detected in subcellular fractions of the islets. These findings indicate that intracellular solubilization of the granules with subsequent diffusion of the insulin into the extracellular space is not a likely mode of insulin secretion in vivo, and suggest that a crystalline zinc-insulin complex may exist in the matrix of the beta granules.
MeSH Terms
Animals
Chemical Phenomena
Chemistry
Crystallization
Cytoplasmic Granules/analysis
Insulin/analysis
Iodine Isotopes
Islets of Langerhans/cytology
Rats
Zinc/analysis
Chemicals
Insulin
Iodine Isotopes
Zinc
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Howell S L
Young D A
Lacy P E
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