共 45 条
RETRACTED: Nicotinamide nucleotide transhydrogenase: A key role in insulin secretion (Retracted article. See vol. 19, pg. 344, 2014)
被引:126
作者:

Freeman, H
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机构: MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England

Shimomura, K
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h-index: 0
机构: MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England

Horner, E
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h-index: 0
机构: MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England

Cox, RD
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h-index: 0
机构:
MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England

Ashcroft, FM
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机构: MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England
机构:
[1] MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England
[2] Univ Oxford, Physiol Lab, Oxford OX1 3PT, England
基金:
英国医学研究理事会;
英国惠康基金;
关键词:
D O I:
10.1016/j.cmet.2005.10.008
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The C57BL/6J mouse displays glucose intolerance and reduced insulin secretion. QTL mapping identified Nicotinamide Nucleotide Transhydrogenase (Nnt), a nuclear-encoded mitochondrial protein thought to be involved in free radical detoxification, as a candidate gene. To investigate its functional role, we used siRNA to knockdown Nnt in insulin-secreting MIN6 cells. This produced a dramatic reduction in insulin secretion and the rise in [Ca2+](i) evoked by glucose, but not tolbutamide. We identified two ENU-induced point mutations in Nnt (N68K, G745D). Nnt mutant mice were glucose intolerant and secreted less insulin during a glucose tolerance test. Isolated islets showed impaired insulin secretion in response to glucose, but not to tolbutamide, and glucose failed to enhance ATP levels. Glucose utilization and production of reactive oxygen species were increased in Nnt 0 cells. We hypothesize that Nnt mutations/deletion uncouple p cell mitochondrial metabolism leading to less ATP production, enhanced K-ATP channel activity, and consequently impaired insulin secretion.
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页码:35 / 45
页数:11
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