The glucose-6-phosphatase system of the glucose sensitive insulin secreting rat insulinoma cells (INS-1) was investigated. INS-1 cells contain easily detectable levels of glucose-6-phosphatase enzyme protein (assessed by Western blotting) and have a very significant enzymatic activity. The features of the enzyme (Km and Vmax values, sensitivity to acidic pH, partial latency, and double immunoreactive band) are similar to those of the hepatic form. On the other hand, hardly detectable levels of glucose-6-phosphatase activity and protein were present in the parent glucose insensitive RINm5F cell line. The mRNA of the glucose-6-phosphate transporter was also more abundant in the INS-1 cells. The results support the view that the glucose-6-phosphatase system of the beta-cell is associated with the regulation of insulin secretion.
Fulceri, R., Kardon, T., Banhegyi, G., Pralong, W.F., Gamberucci, A., Marcolongo, P., et al. (2000). Glucose-6-phosphatase in the insulin secreting cell line INS-1. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 275(1), 103-107 [10.1006/bbrc.2000.3228].
Glucose-6-phosphatase in the insulin secreting cell line INS-1
FULCERI, R.;GAMBERUCCI, A.;MARCOLONGO, P.;BENEDETTI, A.
2000-01-01
Abstract
The glucose-6-phosphatase system of the glucose sensitive insulin secreting rat insulinoma cells (INS-1) was investigated. INS-1 cells contain easily detectable levels of glucose-6-phosphatase enzyme protein (assessed by Western blotting) and have a very significant enzymatic activity. The features of the enzyme (Km and Vmax values, sensitivity to acidic pH, partial latency, and double immunoreactive band) are similar to those of the hepatic form. On the other hand, hardly detectable levels of glucose-6-phosphatase activity and protein were present in the parent glucose insensitive RINm5F cell line. The mRNA of the glucose-6-phosphate transporter was also more abundant in the INS-1 cells. The results support the view that the glucose-6-phosphatase system of the beta-cell is associated with the regulation of insulin secretion.File | Dimensione | Formato | |
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https://hdl.handle.net/11365/30885
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