AUTOCRINE REGULATION OF PARATHYROID SECRETION - INHIBITION OF SECRETION BY CHROMOGRANIN-A (SECRETORY PROTEIN-I) AND POTENTIATION OF SECRETION BY CHROMOGRANIN-A AND PANCREASTATIN ANTIBODIES

被引:58
|
作者
FASCIOTTO, BH
GORR, SU
BOURDEAU, AM
COHN, DV
机构
[1] UNIV LOUISVILLE,HLTH SCI CTR,SCH DENT,DEPT ORAL HLTH,LOUISVILLE,KY 40292
[2] UNIV LOUISVILLE,HLTH SCI CTR,SCH MED,DEPT BIOCHEM,LOUISVILLE,KY 40292
[3] HOP NECKER ENFANTS MALAD,CNRS,UA 583,F-75730 PARIS 15,FRANCE
关键词
D O I
10.1210/endo-127-3-1329
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chromogranin-A, also referred to as secretory protein-I, is a 50-kDa protein present in and secreted by most endocrine cells together with the native hormone. Porcine chromogranin- A contains a sequence identical to pancreastatin, suggesting that it is the precursor of pancreastatin. Pancreastatin is a potent inhibitor of parathyroid gland secretion, and it and chromogranin-A inhibit glucose-stimulated insulin release by the pancreas. It is possible that chromogranin-A, pancreastatin, or a related peptide is a physiological inhibitor of secretion by the parathyroid as well as other endocrine glands. As a test of this hypothesis, parathyroid cells in culture were incubated with purified porcine chromogranin-A or antisera to chromogranin- A and pancreastatin. In the absence of exogenous chromogranin- A or antisera, secretion of chromogranin-A and PTH at 0.5 mM Ca2+was about twice that at 3.0 mM Ca2+. When intact chromogranin- A was added to the incubation medium at 0.5 mM Ca2+, secretion was reduced to the basal level obtained at 3.0 mM Ca2+. Chromogranin-A did not affect the secretion of cells incubated at 3.0 mM Ca2+. At 1 h of incubation, 100 nM chromogranin- A was equivalent in potency to 1 nM pancreastatin, but after 3 h the two agents were equipotent. This suggests that chromogranin-A was processed into biologically active peptide(s) during incubation. Antisera directed against chromogranin-A or pancreastatin potentiated the secretion of both chromogranin- A and PTH at 0.5 mM, but not 3.0 mM, Ca2+. This stimulatory action of the antisera was dose dependent from 1:3200 to 1:400 final dilution, was effective within 2 h, and did not shift the Ca2+set-point for glandular secretion. These results are consonant with chromogranin-A-derived peptides serving as an autocrine inhibitor of parathyroid gland secretion. © 1990 by The Endocrine Society.
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页码:1329 / 1335
页数:7
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