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DNA合成和有丝分裂克隆扩增并非3T3-L1前脂肪细胞分化为脂肪细胞的必要步骤。

DNA synthesis and mitotic clonal expansion is not a required step for 3T3-L1 preadipocyte differentiation into adipocytes.

作者信息

Qiu Z, Wei Y, Chen N, Jiang M, Wu J, Liao K

机构信息

State Laboratory of Molecular Biology, Institute of Biochemistry and Cell Biology and Shanghai Research Center of Life Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China 200031.

出版信息

J Biol Chem. 2001 Apr 13;276(15):11988-95. doi: 10.1074/jbc.M011729200. Epub 2001 Jan 16.

Abstract

Upon differentiation induction of 3T3-L1 preadipocytes by a hormone mixture containing 1-isobutyl-3-methylxanthine, dexamethasone, and insulin, the preadipocytes undergo approximately 2 rounds of mitotic clonal expansion, which just precedes the adipogenic gene expression program and has been thought to be an essential early step for differentiation initiation. By inducing 3T3-L1 preadipocytes with each individual hormone, it was determined that the mitotic clonal expansion was induced only by insulin and not by 1-isobutyl-3-methylxanthine or dexamethasone. Cell number counting and fluorescence-activated cell-sorting analysis indicated that a significant fraction of 3T3-L1 preadipocytes differentiated into adipocytes without mitotic clonal expansion when induced with the combination of 1-isobutyl-3-methylxanthine and dexamethasone. Furthermore, when normally induced 3T3-L1 preadipocytes were treated with PD98059 (an inhibitor of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1) to block the activation of extracellular signal-regulated kinase (Erk) 1 and Erk2, the mitotic clonal expansion was blocked, but adipocyte differentiation was not affected. These observations were confirmed by bromodeoxyuridine labeling. The differentiated adipocytes induced with 1-isobutyl-3-methylxanthine and dexamethasone or standard hormone mixture plus PD98059 were not labeled by bromodeoxyuridine. Thus, it is evident that 3T3-L1 preadipocytes could differentiate into adipocytes without DNA synthesis and mitotic clonal expansion. Our results also suggested that activation of Erk1 and Erk2 is essential to but not sufficient for induction of mitotic clonal expansion.

摘要

在用含有1-异丁基-3-甲基黄嘌呤、地塞米松和胰岛素的激素混合物诱导3T3-L1前脂肪细胞分化时,前脂肪细胞会经历约2轮有丝分裂克隆扩增,这一过程恰好在脂肪生成基因表达程序之前发生,并且一直被认为是分化起始的一个重要早期步骤。通过用每种单独的激素诱导3T3-L1前脂肪细胞,确定有丝分裂克隆扩增仅由胰岛素诱导,而不是由1-异丁基-3-甲基黄嘌呤或地塞米松诱导。细胞计数和荧光激活细胞分选分析表明,当用1-异丁基-3-甲基黄嘌呤和地塞米松联合诱导时,相当一部分3T3-L1前脂肪细胞在没有有丝分裂克隆扩增的情况下分化为脂肪细胞。此外,当用PD98059(一种丝裂原活化蛋白激酶/细胞外信号调节激酶激酶1的抑制剂)处理正常诱导的3T3-L1前脂肪细胞以阻断细胞外信号调节激酶(Erk)1和Erk2的激活时,有丝分裂克隆扩增被阻断,但脂肪细胞分化未受影响。这些观察结果通过溴脱氧尿苷标记得到证实。用1-异丁基-3-甲基黄嘌呤和地塞米松或标准激素混合物加PD98059诱导的分化脂肪细胞未被溴脱氧尿苷标记。因此,很明显3T3-L1前脂肪细胞可以在没有DNA合成和有丝分裂克隆扩增的情况下分化为脂肪细胞。我们的结果还表明,Erk1和Erk2的激活对于诱导有丝分裂克隆扩增是必不可少的,但并不充分。

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