Suppr超能文献

丁酸钠与胰岛素或地塞米松联合使用可使活跃增殖的瑞士3T3细胞终末分化为脂肪细胞。

Sodium butyrate in combination with insulin or dexamethasone can terminally differentiate actively proliferating Swiss 3T3 cells into adipocytes.

作者信息

Toscani A, Soprano D R, Soprano K J

机构信息

Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.

出版信息

J Biol Chem. 1990 Apr 5;265(10):5722-30.

PMID:2180933
Abstract

Sodium butyrate arrests the growth of actively proliferating Swiss 3T3 cells. A previous report from our laboratory describes the pattern of expression of a representative group of growth-associated genes following treatment of Swiss 3T3 cells with sodium butyrate. The results of this study suggest that sodium butyrate-induced growth arrest involves events which lead to adipocyte differentiation (Toscani, A., Soprano, D.R., and Soprano, K.J. (1988) Oncogene Res. 3, 233-238). However, while sodium butyrate by itself could apparently initiate adipogenesis, it alone was not sufficient to maintain this differentiation state. We now wish to further characterize the role of sodium butyrate in adipocyte differentiation. Subconfluent cultures of Swiss 3T3 cells were treated with sodium butyrate in combination with other agents known to induce Swiss 3T3 cell adipogenesis (e.g. 1-methyl-3-isobutylxanthine, insulin, and dexamethasone) and then analyzed at various times thereafter for: (a) the presence of high concentrations of intracellular lipid as detected by microscopic examination of treated cells following staining with lipid-specific dyes and (b) the expression of four genes known to be modulated during the differentiation of preadipocytes into mature adipocytes (actin, adipsin, lipoprotein lipase, and adipocyte P2). Our results show that sodium butyrate in combination with either insulin or dexamethasone can fully differentiate Swiss 3T3 cells into adipocytes, at least as determined by accumulation of high levels of intracellular lipid. Moreover, the sodium butyrate-mediated process of differentiation can occur in subconfluent, actively proliferating cells. Thus, these experiments describe a new, previously unidentified activity of sodium butyrate and also suggest that this model system may be a useful one to study the relationship between growth arrest and differentiation.

摘要

丁酸钠可抑制活跃增殖的瑞士3T3细胞的生长。我们实验室之前的一份报告描述了用丁酸钠处理瑞士3T3细胞后,一组代表性生长相关基因的表达模式。这项研究的结果表明,丁酸钠诱导的生长停滞涉及导致脂肪细胞分化的事件(托斯卡尼,A.,索普拉诺,D.R.,和索普拉诺,K.J.(1988年)《癌基因研究》3,233 - 238)。然而,虽然丁酸钠本身显然可以启动脂肪生成,但仅靠它不足以维持这种分化状态。我们现在希望进一步阐明丁酸钠在脂肪细胞分化中的作用。用丁酸钠与其他已知可诱导瑞士3T3细胞脂肪生成的试剂(如1 - 甲基 - 3 - 异丁基黄嘌呤、胰岛素和地塞米松)联合处理亚汇合的瑞士3T3细胞培养物,然后在之后的不同时间分析:(a)用脂质特异性染料染色后,通过显微镜检查处理过的细胞检测到的高浓度细胞内脂质的存在情况,以及(b)已知在前脂肪细胞分化为成熟脂肪细胞过程中被调节的四个基因(肌动蛋白、脂肪酶、脂蛋白脂肪酶和脂肪细胞P2)的表达情况。我们的结果表明,丁酸钠与胰岛素或地塞米松联合使用可以使瑞士3T3细胞完全分化为脂肪细胞,至少通过高水平细胞内脂质的积累来确定。此外,丁酸钠介导的分化过程可以在亚汇合的、活跃增殖的细胞中发生。因此,这些实验描述了丁酸钠一种新的、以前未被识别的活性,也表明这个模型系统可能是研究生长停滞与分化之间关系的有用系统。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验