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SCL基因产物在髓系白血病细胞分化过程中受细胞因子反应调控,并对其产生差异性调节。

The SCL gene product is regulated by and differentially regulates cytokine responses during myeloid leukemic cell differentiation.

作者信息

Tanigawa T, Elwood N, Metcalf D, Cary D, DeLuca E, Nicola N A, Begley C G

机构信息

Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.

出版信息

Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7864-8. doi: 10.1073/pnas.90.16.7864.

Abstract

Differentiation induction in murine M1 leukemia cells by interleukin 6 (IL-6), leukemia inhibitory factor (LIF), and oncostatin M (OSM) is postulated to occur via a common receptor chain, gp130. In this study, growth factor-induced differentiation of M1 cells was accompanied by a late and persistent decrease in levels of mRNA and protein for a helix-loop-helix transcription factor, the SCL gene product. To evaluate whether reduced SCL expression was instrumental in monocyte differentiation, an SCL cDNA expression vector was introduced into M1 cells to obtain cell lines in which overexpression of SCL mRNA and protein was enforced. This resulted in a reduction in cells differentiating in response to LIF and OSM but not in response to IL-6. Scatchard analysis indicated that both parental and SCL-transfected cell lines exhibited similar receptor numbers and receptor affinities for LIF, OSM, and IL-6, suggesting that the differential responsiveness was not due to selective receptor down-modulation. Thus, these data implicate SCL in monocytic differentiation and provide evidence for differential receptor signaling pathways despite utilization of a common gp130 subunit by all three receptors.

摘要

白细胞介素6(IL-6)、白血病抑制因子(LIF)和制瘤素M(OSM)对小鼠M1白血病细胞的分化诱导被认为是通过一条共同的受体链gp130发生的。在本研究中,生长因子诱导的M1细胞分化伴随着一种螺旋-环-螺旋转录因子(SCL基因产物)的mRNA和蛋白质水平的晚期持续性降低。为了评估SCL表达降低是否对单核细胞分化起作用,将一个SCL cDNA表达载体导入M1细胞以获得SCL mRNA和蛋白质过表达的细胞系。这导致对LIF和OSM有反应而分化的细胞减少,但对IL-6有反应而分化的细胞没有减少。Scatchard分析表明,亲代细胞系和SCL转染细胞系对LIF、OSM和IL-6均表现出相似的受体数量和受体亲和力,提示差异反应性并非由于选择性受体下调所致。因此,这些数据表明SCL参与单核细胞分化,并为尽管三种受体都利用共同的gp130亚基但存在差异的受体信号通路提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/735f/47243/2a7c1bf8a07e/pnas01473-0450-a.jpg

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