Depletion of SK1 channel subunits leads to constitutive insulin secretion

被引:13
作者
Andres, Marilou A. [1 ]
Baptista, Nicholas C. [1 ]
Efird, Jimmy T. [1 ,2 ,4 ]
Ogata, Kathleen K. [2 ,3 ]
Bellinger, Frederick P. [2 ]
Zeyda, Thomas [2 ]
机构
[1] Univ Hawaii, Pacific Biomed Res Ctr, Honolulu, HI 96822 USA
[2] Univ Hawaii, John A Burns Sch Med, Honolulu, HI 96813 USA
[3] Univ Hawaii, Kapiolani Community Coll, Honolulu, HI 96816 USA
[4] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA
关键词
Afterhyperpolarization; Beta cell; Insulin secretion; SK potassium channel; Heteromeric channel; Diabetic; CA2+-ACTIVATED K+ CHANNELS; PANCREATIC BETA-CELLS; ACTIVATED POTASSIUM CHANNEL; SMALL-CONDUCTANCE; ACTION-POTENTIALS; FUNCTIONAL EXPRESSION; ELECTRICAL-ACTIVITY; CYTOPLASMIC CA2+; HEK-293; CELLS; RAT-BRAIN;
D O I
10.1016/j.febslet.2008.12.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the pancreas, the role of the small-conductance, calcium-activated SK channels remains controversial. Here, we show that three SK subtypes are expressed in the rat insulinoma cells. Our findings demonstrate that rat SK1 (rSK1) channels ensure appropriate insulin secretion by establishing the cell's negative resting membrane potential and shortening the duration of the action potential. We also found that the depletion of rSK1 transcripts generated a condition in which beta cells constitutively secrete insulin, even in the absence of a stimulating molecule (such as glucose). Together, these results implicate SK1 subunits as key regulators of excitability and endocrine function in beta cells. Published by Elsevier B. V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:369 / 376
页数:8
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