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肿瘤坏死因子杀伤细胞的两种机制的证据。

Evidence for two mechanisms by which tumor necrosis factor kills cells.

作者信息

Reid T R, Torti F M, Ringold G M

机构信息

Department of Cancer, Syntex Research, Palo Alto, California 94303.

出版信息

J Biol Chem. 1989 Mar 15;264(8):4583-9.

PMID:2925656
Abstract

Tumor necrosis factor (TNF) can inhibit the differentiation of preadipocytes to adipocytes and will revert differentiated adipocytes to the preadipocyte state. TNF is not toxic to either adipocytes or preadipocytes when used alone but is highly toxic to these cells when used in conjunction with cycloheximide, yielding virtually 100% killing within 4-6 h of treatment. A cell line (TA1 R-6) was isolated which is resistant to the combined toxic effects of TNF and cycloheximide. This cell line is stable and, unlike the parental cell line, does not morphologically differentiate to adipocytes or express adipocyte-specific mRNAs. It has a more transformed appearance and growth pattern and, while resistant to the toxic effects of TNF and cycloheximide in a 6-h assay, has become sensitive to cytotoxicity induced by TNF used alone in a 3-day assay. The adipocyte differentiation-inducing agents, dexamethasone and indomethacin, block the cytotoxicity induced by TNF alone in the TA1 R-6 line but do not block the rapid cytotoxicity of TNF and cycloheximide in the parental line. These results provide both genetic and pharmacologic evidence that there are at least two distinct or overlapping pathways by which TNF mediates its effects.

摘要

肿瘤坏死因子(TNF)可抑制前脂肪细胞向脂肪细胞的分化,并使已分化的脂肪细胞恢复到前脂肪细胞状态。TNF单独使用时对脂肪细胞或前脂肪细胞均无毒性,但与环己酰亚胺联合使用时对这些细胞具有高度毒性,在处理4 - 6小时内几乎可导致100%的细胞死亡。分离出了一种细胞系(TA1 R - 6),它对TNF和环己酰亚胺的联合毒性作用具有抗性。该细胞系稳定,与亲代细胞系不同,它在形态上不会分化为脂肪细胞,也不表达脂肪细胞特异性mRNA。它具有更具转化性的外观和生长模式,虽然在6小时的实验中对TNF和环己酰亚胺的毒性作用具有抗性,但在3天的实验中对单独使用TNF诱导的细胞毒性变得敏感。脂肪细胞分化诱导剂地塞米松和吲哚美辛可阻断TA1 R - 6细胞系中单独由TNF诱导的细胞毒性,但不能阻断亲代细胞系中TNF和环己酰亚胺的快速细胞毒性。这些结果提供了遗传学和药理学证据,表明TNF介导其作用至少有两条不同或重叠的途径。

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