Rondinone C M, Rodbard D, Baker M E
Laboratory of Theoretical and Physical Biology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Endocrinology. 1993 Jun;132(6):2421-6. doi: 10.1210/endo.132.6.8504747.
We find that 1-10 nM aldosterone can induce differentiation of 3T3-L1 cells into adipose cells as evaluated by microscopic accumulation of fat droplets and quantitative measurement of triglycerides and of glycerol-3-phosphate dehydrogenase, an enzyme specific for adipocyte differentiation. Moreover, the aldosterone antagonist ZK91587 inhibits aldosterone-but not glucocorticoid-mediated differentiation of 3T3-L1 cells. Steroid binding assays with 3T3-L1 cells indicate the presence of specific binding sites for aldosterone. We conclude that there is an aldosterone receptor-mediated pathway for terminal differentiation of 3T3-L1 cells into adipose cells. Receptors for aldosterone have also been found in a variety of cells that do not function to regulate sodium and potassium transport. The aldosterone receptor may have a role in regulation expression of genes involved in differentiation of these cells.
我们发现,通过显微镜观察脂肪滴的积累以及对甘油三酯和甘油-3-磷酸脱氢酶(一种脂肪细胞分化特异性酶)进行定量测量来评估,1-10 nM的醛固酮可诱导3T3-L1细胞分化为脂肪细胞。此外,醛固酮拮抗剂ZK91587可抑制醛固酮介导的3T3-L1细胞分化,但不抑制糖皮质激素介导的分化。对3T3-L1细胞进行的类固醇结合试验表明存在醛固酮的特异性结合位点。我们得出结论,存在一条醛固酮受体介导的途径,可使3T3-L1细胞终末分化为脂肪细胞。在多种不参与调节钠钾转运的细胞中也发现了醛固酮受体。醛固酮受体可能在调控这些细胞分化相关基因的表达中发挥作用。