MORPHOLOGICAL AND FUNCTIONAL-CHARACTERIZATION OF BETA-TC-6 CELLS - AN INSULIN-SECRETING CELL-LINE DERIVED FROM TRANSGENIC MICE
MORPHOLOGICAL AND FUNCTIONAL-CHARACTERIZATION OF BETA-TC-6 CELLS - AN INSULIN-SECRETING CELL-LINE DERIVED FROM TRANSGENIC MICE
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DOI：
10.2337/diabetes.44.3.306
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发表时间：
1995-03-01
期刊：
影响因子：
7.7
通讯作者：
ROBERTSON, RP
中科院分区：
文献类型：
--
作者：
POITOUT, V;STOUT, LE;ROBERTSON, RP
Morphological analysis of hormone content and functional assessment of hormone secretion were conducted in beta TC-6 cells, an insulin-secreting cell. line derived from transgenic mice expressing the large T-antigen of simian virus 40 (SV40) in pancreatic beta-cells. We observed by immunohistochemistry and confocal microscopy that beta TC-6 cells contain abundant insulin and small amounts of glucagon and somatostatin (SRIF), Glucagon usually co-localized with insulin, whereas cells containing SRIF did not contain insulin or glucagon, Static incubation and perifusion experiments demonstrated that beta TC-6 cells at passage 30-45 secrete insulin in response to glucose, In static incubations, maximal stimulation was achieved for glucose concentrations > 2.8 mmol/l glucose, and the half-maximal effect was observed at 0.5 mmol/l, Maximal stimulation was four times greater than HIT-T15 cells at passage 72-81, although HIT cells had a greater response over their basal levels, The magnitude of the insulin response to glucose in perifusion was 1,734 +/- 384 pmol . l(-1). min acid was 4.6-fold greater in the presence of 3-isobutyl-1-methylxanthine. Low amounts of glucagon were released in response to amino acids. Epinephrine (EPI), and to a lesser extent SRIF, inhibited phasic glucose-induced insulin secretion, A major portion of these inhibitory effects was mediated by pertussis toxin-sensitive substrates. Immunoblots detected the presence of the G-proteins Gi alpha 2, Gi alpha 3, and Go alpha 2. These results indicate that beta TC-6 cells are a glucose-responsive cell line in which insulin exocytosis is physiologically regulated by EPI and SRIF through Gi/Go-mediated mechanisms.
