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Inhibition of Insulin Secretion by Betagranin, an N-terminal Chromogranin A Fragment
- Source :
- Journal of Biological Chemistry, Vol. 282, No 17 (2007) pp. 12717-24
- Publication Year :
- 2007
- Publisher :
- Elsevier BV, 2007.
-
Abstract
- Betagranin, an N-terminal fragment of chromogranin A, results from a proteolytic processing, and is co-secreted with insulin. While other chromogranin A-derived peptides negatively modulate hormone secretion, the role of betagranin in pancreatic beta-cells is so far unknown. We have recently shown that pancreatic islet betagranin levels are down-regulated in obese, leptin-deficient mice. In the present study, we have investigated the distribution of betagranin in primary mouse islets and cells of the MIN6 line and have evaluated its effects on insulin secretion. We showed that betagranin co-localizes with insulin within secretory granules and strongly inhibited insulin secretion in response to both glucose and potassium, by blocking the influx of calcium. The data demonstrated a hitherto unknown inhibitory effect of betagranin on insulin secretion.
- Subjects :
- endocrine system
medicine.medical_specialty
medicine.medical_treatment
Potassium
chemistry.chemical_element
Calcium
Biochemistry
Cell Line
Islets of Langerhans
Mice
Potassium/metabolism/pharmacology
Internal medicine
Insulin Secretion
Chromogranins
medicine
Animals
Insulin
Distribution (pharmacology)
Sweetening Agents/pharmacology
Secretion
Calcium Signaling
ddc:576
Molecular Biology
Insulin/secretion
Islets of Langerhans/metabolism/ultrastructure
geography
geography.geographical_feature_category
biology
Chromogranin A
Chromogranins/pharmacology
Cell Biology
Islet
Glucose
Endocrinology
chemistry
Sweetening Agents
Calcium Signaling/drug effects
biology.protein
Glucose/metabolism/pharmacology
Female
Hormone
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 282
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi.dedup.....bce15593c26062f90e2a91dc71f388d7