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Publication : IP3 receptor types 2 and 3 mediate exocrine secretion underlying energy metabolism.

First Author  Futatsugi A Year  2005
Journal  Science Volume  309
Issue  5744 Pages  2232-4
PubMed ID  16195467 Mgi Jnum  J:101380
Mgi Id  MGI:3603902 Doi  10.1126/science.1114110
Citation  Futatsugi A, et al. (2005) IP3 receptor types 2 and 3 mediate exocrine secretion underlying energy metabolism. Science 309(5744):2232-4
abstractText  Type 2 and type 3 inositol 1,4,5-trisphosphate receptors (IP3R2 and IP3R3) are intracellular calcium-release channels whose physiological roles are unknown. We show exocrine dysfunction in IP3R2 and IP3R3 double knock-out mice, which caused difficulties in nutrient digestion. Severely impaired calcium signaling in acinar cells of the salivary glands and the pancreas in the double mutants ascribed the secretion deficits to a lack of intracellular calcium release. Despite a normal caloric intake, the double mutants were hypoglycemic and lean. These results reveal IP3R2 and IP3R3 as key molecules in exocrine physiology underlying energy metabolism and animal growth.
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