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The Life Cycle of the Gastrin Granule

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Journal Cell Tissue Res
Date 1982 Jan 1
PMID 7037192
Citations 13
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Abstract

The ultrastructure of gastrin cells in the rat antrum was analyzed with standardized and quantitative planimetric methods. Resting and active cells were compared. The gastrin cells were activated by removal of the acid-producing part of the stomach (fundectomy). As a result of the serum gastrin concentrations were greatly elevated. Compared with gastrin cells in fasted control rats the gastrin cells in fundectomized rats were increased in number, contained fewer cytoplasmic granules, increased amount of endoplasmic reticulum, and an enlarged Golgi area. Generally, the secretory granules of the gastrin cell displayed a wide range of electron density from highly electron-dense to electron-lucent. They exhibited certain characteristic features: 1) Electron-dense granules made up a greater proportion of the total granule population in active gastrin cells than in resting cells. 2) Electron-dense granules were more frequent near the Golgi stacks than in the periphery of the cell. 3) Electron-dense granules were smaller in size than the electron-lucent granules; hence, small electron-dense granules probably represent young granules (progranules), while large, electron-lucent granules represent mature (old) granules. 4) Electron-dense granules invariably displayed a more intense immunoreactivity than electron-lucent granules. The gastrins are generated from a large precursor molecule. The post-translational processing of this precursor is reflected in the gastrin-component pattern. The gastrin-component pattern in antral extracts of fundectomized and normal fasting rats differed in that the proportion of the gastrin-4-like component was reduced, whereas the gastrin-34-like component was increased in the fundectomized rats. The results suggest a greater proportion of small gastrin components in the mature granules than in the newly formed ones, presumably due to more extensive conversion of larger forms into smaller forms with a longer granule half-life. As a result gastrin-17- and gastrin-34-like components make up a larger proportion of total gastrin in active gastrin cells than in resting gastrin cells.

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References
1.
Larsson L . Gastrin and ACTH-like immunoreactivity occurs in two ultrastructurally distinct cell types of rat antropyloric mucosa. Evidence for a non-parallel processing of the peptides during feeding and fasting. Histochemistry. 1978; 58(1-2):33-48. DOI: 10.1007/BF00489947. View

2.
Rehfeld J, Stadil F, Rubin B . Production and evaluation of antibodies for the radioimmunoassay of gastrin. Scand J Clin Lab Invest. 1972; 30(2):221-32. DOI: 10.3109/00365517209081114. View

3.
Rehfield J, Uvnas-Wallensten K . Gastrins in cat and dog: evidence for a biosynthetic relationship between the large molecular forms of gastrin and heptadecapeptide gastrin. J Physiol. 1978; 283:379-96. PMC: 1282784. DOI: 10.1113/jphysiol.1978.sp012507. View

4.
Rehfeld J . Four basic characteristics of the gastrin-cholecystokinin system. Am J Physiol. 1981; 240(4):G255-66. DOI: 10.1152/ajpgi.1981.240.4.G255. View

5.
Mortensen N, Morris J, Owens C . Gastrin and the ultrastructure of G cells after stimulation with acetylcholine. Cell Tissue Res. 1978; 192(3):513-25. DOI: 10.1007/BF00212330. View