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首页> 外文期刊>Immunobiology: Zeitschrift fur Immunitatsforschung >Activating transcription factor 3 (ATF3) promotes sublytic C5b-9-induced glomerular mesangial cells apoptosis through up-regulation of Gadd45alpha and KLF6 gene expression.
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Activating transcription factor 3 (ATF3) promotes sublytic C5b-9-induced glomerular mesangial cells apoptosis through up-regulation of Gadd45alpha and KLF6 gene expression.

机译:激活转录因子3(ATF3)通过上调Gadd45alpha和KLF6基因表达来促进C5b-9诱导的肾小球系膜细胞凋亡。

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摘要

The sublytic C5b-9 complexes can result in glomerular mesangial cells (GMCs) apoptosis, which involved in the initiation and development of rat Thy-1 nephritis. Activating transcription factor 3 (ATF3) is an immediate early gene for cells to cope with a variety of stress signals, and our previous study revealed that ATF3 could promote GMCs apoptosis attacked by sublytic C5b-9. But the mechanism of ATF3 promoting GMCs apoptosis triggered by sublytic C5b-9 attack has not been elucidated. In this study, the data showed that the expression of ATF3, growth arrest and DNA damage-45 alpha (Gadd45alpha), Kruppel-like factor 6 (KLF6) and proliferating cell nuclear antigen (PCNA) in the GMCs in response to sublytic C5b-9 stimulation for the indicated time was significantly increased, and ATF3 expression could lead to GMCs apoptosis through up-regulation of Gadd45alpha and KLF6, but not up-regulation of PCNA. Furthermore, Gadd45alpha was identified as a downstream target gene regulated by ATF3 directly, and KLF6 might be regulated by ATF3 in an indirect manner.
机译:分解型C5b-9复合物可导致肾小球系膜细胞(GMC)凋亡,这与大鼠Thy-1肾炎的发生和发展有关。激活转录因子3(ATF3)是细胞应对各种应激信号的直接早期基因,而我们先前的研究表明ATF3可以促进C5b-9裂解攻击GMCs的细胞凋亡。但是尚不清楚ATF3促进C5b-9裂解攻击引发GMCs凋亡的机制。在这项研究中,数据显示AMC3对C5b-分解酶的反应是AMC3,生长停滞和DNA损伤-45 alpha(Gadd45alpha),Kruppel样因子6(KLF6)和增殖细胞核抗原(PCNA)的表达。在指定时间内9刺激显着增加,并且ATF3表达可能通过上调Gadd45alpha和KLF6而不是PCNA上调导致GMCs凋亡。此外,Gadd45alpha被鉴定为直接由ATF3调控的下游靶基因,而KLF6可能由ATF3间接调控。

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