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首页> 外文期刊>Journal of cellular biochemistry. >Mice Deficient in CIZ/NMP4 Develop an Attenuated Form of K/BxN-Serum Induced Arthritis
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Mice Deficient in CIZ/NMP4 Develop an Attenuated Form of K/BxN-Serum Induced Arthritis

机译:缺乏CIZ / NMP4的小鼠产生衰减形式的K / BXN-血清诱导的关节炎

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摘要

CIZ/NMP4 (Cas interacting zinc finger protein, Nmp4, Zfp384) is a transcription factor that is known to regulate matrix related-proteins. To explore the possible pathophysiological role of CIZ/NMP4 in arthritis, we examined CIZ/NMP4 expression in articular cartilage in arthritis model. CIZ/NMP4 was expressed in the articular chondrocytes of mice at low levels while its expression was enhanced when arthritis was induced. Arthritis induction increased clinical score in wild type mice. In contrast, CIZ/NMP4 deficiency suppressed such rise in the levels of arthritis score and swelling of soft tissue. CIZ/NMP4 deficiency also reduced invasion of inflammatory cells in joint tissue. Quantitative PCR analyses of mRNA from joints revealed that arthritis-induced increase in expressions of IL-1 (3 was suppressed by CIZ/ NMP4 deficiency. CIZ/NMP4 bound to IL-1 (3 promoter and activated its transcription. The increase in CIZ/NMP4 in arthritis was also associated with enhancement in bone resorption and cartilage matrix degradation. In fact, RANKL, a signaling molecule prerequisite for osteoclastogenesis and, MMP-3, a clinical marker for arthritis were increased in joints upon arthritis induction. In contrast, CIZ/NMP4 deficiency suppressed the arthritis-induced increase in bone resorption, expression of RANKL and MMP-3 mRNA. Thus, CIZ/NMP4 plays a role in the development of arthritis at least in part through regulation of key molecules related to the arthritis. J. Cell. Biochem. 117: 970-977, 2016.
机译:CIZ / NMP4(CAS相互作用锌手指蛋白,NMP4,ZFP384)是已知调节基质相关蛋白的转录因子。为了探讨CIZ / NMP4在关节炎中可能的病理生理作用,我们在关节炎模型中检查了在关节软骨中的CIZ / NMP4表达。 Ciz / NMP4在低水平的小鼠的关节软骨细胞中表达,而当诱导关节炎时,其表达增强。关节炎诱导在野生型小鼠中增加临床评分。相比之下,CIZ / NMP4缺陷抑制了关节炎评分和软组织肿胀水平的升高。 CIZ / NMP4缺乏还降低了关节组织中炎性细胞的侵袭。来自关节的mRNA的定量PCR分析显示,IL-1(3的CIZ / NMP4缺乏抑制的关节炎诱导的升高(3次抑制CIZ / NMP4缺乏。与IL-1结合的CIZ / NMP4(3启动子并激活其转录。CIZ / CIZ的增加/关节炎中的NMP4也与骨吸收和软骨血管基质降解的增强相关。实际上,关节炎诱导关节的关节增加了对骨核细胞发生和MMP-3,关节炎的临床标志物的信号分子先决条件。相比之下,CIZ / NMP4缺乏抑制了骨吸收中的关节炎诱导的骨吸收增加,RANKL和MMP-3 mRNA的表达。因此,CIZ / NMP4至少通过调节与关节炎相关的关键分子的调节在关节炎的发展中起作用。J 。细胞。Biochem。117:970-977,2016。

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