磷酸烯醇丙酮酸羧激酶
糖原
葡萄糖稳态
内分泌学
内科学
生物
能量稳态
褐色脂肪组织
平衡
突变体
脂肪组织
基因剔除小鼠
基因表达
产热
基因敲除
糖原合酶
基因
生物化学
医学
糖尿病
肥胖
胰岛素抵抗
作者
Nai-dy Wang,Milton J. Finegold,Allan Bradley,Ching N. Ou,Sandy V. Abdelsayed,Margaret Wilde,Lorna Taylor,Debra Rose Wilson,Gretchen J. Darlington
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1995-08-25
卷期号:269 (5227): 1108-1112
被引量:937
标识
DOI:10.1126/science.7652557
摘要
Mice homozygous for the targeted deletion of the c/ebp α gene, which expresses the CCAAT/enhancer-binding protein α (C/EBPα), did not store hepatic glycogen and died from hypoglycemia within 8 hours after birth. In these mutant mice, the amounts of glycogen synthase messenger RNA were 50 to 70 percent of normal and the transcriptional induction of the genes for two gluconeogenic enzymes, phosphoenolpyruvate carboxykinase and glucose-6-phosphatase, was delayed. The hepatocytes and adipocytes of the mutant mice failed to accumulate lipid and the expression of the gene for uncoupling protein, the defining marker of brown adipose tissue, was reduced. This study demonstrates that C/EBPα is critical for the establishment and maintenance of energy homeostasis in neonates.
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