Cell-specific processing of chromogranin A in endocrine cells of the rat stomach

被引:31
作者
Norlén, P
Curry, WJ
Björkqvist, M
Maule, A
Cunningham, RT
Hogg, RB
Harriott, P
Johnston, CF
Hutton, JC
Håkanson, R
机构
[1] Lund Univ, Dept Pharmacol, Inst Physiol Sci, S-22362 Lund, Sweden
[2] Queens Univ Belfast, Dept Med, Belfast, Antrim, North Ireland
[3] Queens Univ Belfast, Sch Biol & Biochem, Belfast, Antrim, North Ireland
[4] Univ Colorado, Hlth Sci Ctr, Barbara Davis Ctr Childhood Diabet, Boulder, CO USA
关键词
chromogranin A; ECL cell; D cell; A-like cell; EC cell; G cell; processing;
D O I
10.1177/002215540104900102
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The rat stomach is rich in endocrine cells. The acid-producing (oxyntic) mucosa contains ECL cells, A-like cells, and somatostatin (D) cells, and the antrum harbours gastrin (G) cells, enterochromaffin (EC) cells and D cells. Although chromogranin A (CgA) occurs in all these cells, its processing appears to differ from one cell type to another. Eleven antisera generated to different regions of rat CgA, two antisera generated to a human (h) CgA sequences, and one to a bovine Ib) CgA sequence, respectively, were employed together with antisera directed towards cell-specific markers such as gastrin (G cells), serotonin (EC cells), histidine decarboxylsae (ECL cells) and somatostatin (D cells) to characterize the expression of CgA and CgA-derived peptides in the various endocrine cell populations of the rat stomach. In the oxyntic mucosa, antisera raised against CgA(291-319) and CGA(316-321) immunostained D cells exclusively, whereas antisera raised against bCgA(82-91) and CgA(121-128) immunostained A-like cells and D cells. Antisera raised against CgA(318-349) and CgA(437-448) immunostained ECL cells and A-like cells, but not D cells. In the antrum, antisera against CgA(291-319) immunostained D cells, and antisera against CgA(351-356) immunostained G cells. Our observations suggest that each individual endocrine cell type in the rat stomach generates a unique mixture of CgA-derived peptides, probably reflecting cell-specific differences in the post-translational processing of CgA and its peptide products. A panel of antisera that recognize specific domains of CgA may help to identify individual endocrine cell populations.
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页码:9 / 18
页数:10
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