TY - JOUR
T1 - Glucose dependence of the regulated secretory pathway in αTC1-6 cells
AU - McGirr, Rebecca
AU - Ejbick, Christina E.
AU - Carter, David E.
AU - Andrews, Joseph D.
AU - Nie, Ying
AU - Friedman, Theodore C.
AU - Dhanvantari, Savita
N1 - Endocrinology. 2005 Oct;146(10):4514-23. Epub 2005 Jun 30. Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
PY - 2005/10
Y1 - 2005/10
N2 - We have investigated the effects of chronically elevated glucose concentrations on the pancreatic α-cell line αTC1-6. We show that basal glucagon secretion and proglucagon gene expression were increased in response to high glucose levels. The extent of acute stimulated secretion of glucagon was also increased in response to high glucose, as was the transcription of the prohormone processing enzymes PC1/3 and PC2. The secretion of GLP-1, a proglucagon-derived peptide produced by cleavage of proglucagon by PC1/3, was also increased in response to high glucose. Gene expression profiling experiments showed that a number of components of the regulated secretory pathway were up-regulated at high glucose concentrations, including processing enzymes and exocytotic proteins. Immunoblot analysis showed that the expression of the exocytotic SNARE proteins, as well as that of PC1/3, chromogranin A, and 7B2, were all increased after chronic exposure to high glucose levels. Immunocytochemistry showed no changes in the expression of the mature α-cell markers glucagon and brn-4 and no induction of the immature α-cell marker pdx-1. We conclude that chronically elevated glucose concentrations up-regulate the regulated secretory response of the α-cell. Copyright © 2005 by The Endocrine Society.
AB - We have investigated the effects of chronically elevated glucose concentrations on the pancreatic α-cell line αTC1-6. We show that basal glucagon secretion and proglucagon gene expression were increased in response to high glucose levels. The extent of acute stimulated secretion of glucagon was also increased in response to high glucose, as was the transcription of the prohormone processing enzymes PC1/3 and PC2. The secretion of GLP-1, a proglucagon-derived peptide produced by cleavage of proglucagon by PC1/3, was also increased in response to high glucose. Gene expression profiling experiments showed that a number of components of the regulated secretory pathway were up-regulated at high glucose concentrations, including processing enzymes and exocytotic proteins. Immunoblot analysis showed that the expression of the exocytotic SNARE proteins, as well as that of PC1/3, chromogranin A, and 7B2, were all increased after chronic exposure to high glucose levels. Immunocytochemistry showed no changes in the expression of the mature α-cell markers glucagon and brn-4 and no induction of the immature α-cell marker pdx-1. We conclude that chronically elevated glucose concentrations up-regulate the regulated secretory response of the α-cell. Copyright © 2005 by The Endocrine Society.
KW - Cell Line
KW - Glucagon-Like Peptide 1
KW - Rats
KW - Glucagon/metabolism
KW - Reverse Transcriptase Polymerase Chain Reaction
KW - Cell Division/drug effects
KW - Protein Precursors/metabolism
KW - Islets of Langerhans/drug effects
KW - Animals
KW - Glucose/pharmacology
KW - Peptide Fragments/metabolism
KW - Kinetics
KW - Proglucagon
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UR - http://www.scopus.com/inward/citedby.url?scp=24944438228&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/4de12a3c-4d8c-3929-aa1b-b779e0915a56/
U2 - 10.1210/en.2005-0402
DO - 10.1210/en.2005-0402
M3 - Article
C2 - 15994347
SN - 0013-7227
VL - 146
SP - 4514
EP - 4523
JO - Endocrinology
JF - Endocrinology
IS - 10
ER -