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视黄酸对3T3-L2细胞脂肪转化的抑制作用。

Inhibition of adipose conversion in 3T3-L2 cells by retinoic acid.

作者信息

Murray T, Russell T R

出版信息

J Supramol Struct. 1980;14(2):255-66. doi: 10.1002/jss.400140214.

Abstract

The role of retinoic acid in modulating the differentiation of 3T3-L2 fibroblasts into adipocytes has been examined. Results indicate that the retinoid is capable of effectively inhibiting the degree of adipose conversion which is brought about by treatment of preadipocytes with 1-methyl-3-isobutylxanthine plus dexamethasone. MOrphological and enzymatic (fatty acid synthetase activity) expression of the adipose phenotype are both inhibited more than 90% by 10(-6) M retinoic acid. The inhibition is concentration dependent with retinoic acid must be administered simultaneously with the triggering agents to be effective. Exposure of nongrowing preadipocytes to retinoic acid does not alter the ability o the cells to differentiate in response to a subsequent treatment with methylisobutylxanthine plus dexamethasone. Further, the inhibition is reversible. Cultures i which methylisobutylxanthine plus dexamethasone triggered differentiation has been blocked by addition of retinoic acid (10(-6) M) will readily undergo adipose conversion in response to a second treatment with methylisobutylxanthine plus dexamethasone in the absence of the retinoid. Similar inhibition of differentiation was found when cultures were treated with drugs in medium supplemented with either newborn calf serum or fetal calf serum. However, the extent to which methylisobutylxanthine plus dexamethasone are able to promote differentiation in these cells is considerably greater in medium containing fetal calf serum.

摘要

视黄酸在调节3T3-L2成纤维细胞向脂肪细胞分化中的作用已得到研究。结果表明,该类视黄醇能够有效抑制脂肪转化程度,这种转化是由用1-甲基-3-异丁基黄嘌呤加地塞米松处理前脂肪细胞所引起的。脂肪表型的形态学和酶学(脂肪酸合成酶活性)表达均被10^(-6) M视黄酸抑制超过90%。这种抑制作用具有浓度依赖性,视黄酸必须与触发剂同时给药才有效。将非生长状态的前脂肪细胞暴露于视黄酸不会改变细胞对随后用甲基异丁基黄嘌呤加地塞米松处理的分化能力。此外,这种抑制是可逆的。在用甲基异丁基黄嘌呤加地塞米松触发分化的培养物中,加入视黄酸(10^(-6) M)会阻止分化,在没有视黄醇的情况下,再次用甲基异丁基黄嘌呤加地塞米松处理时,这些培养物将很容易发生脂肪转化。当培养物在补充有新生牛血清或胎牛血清的培养基中用药物处理时,也发现了类似的分化抑制。然而,在含有胎牛血清的培养基中,甲基异丁基黄嘌呤加地塞米松促进这些细胞分化的程度要大得多。

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