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Jak/STAT 信号通路在视网膜变性中的差异作用。

The differential role of Jak/STAT signaling in retinal degeneration.

机构信息

Department of Ophthalmology, University of Zurich, Zurich, Switzerland.

出版信息

Adv Exp Med Biol. 2010;664:601-7. doi: 10.1007/978-1-4419-1399-9_69.

Abstract

Retinal degenerative diseases are a major cause of severe visual impairment or blindness in humans. To develop therapeutic strategies it is of particular importance to understand the molecular mechanisms taking place during the progression of the disease. Genes and proteins of the Janus kinase/Signal Transducer and Activator of Transcription (Jak/STAT) signaling pathway have been shown to play an important role in models of retinal degeneration (RD). Here we investigated the expression of additional genes involved in the Jak/STAT pathway in an induced (light exposure) and an inherited (rd1 mouse) model of RD. We show that STAT mRNAs as well as the Jak2/shp-1 pathway are differentially regulated in the two models. In contrast, we show that Jak3 mRNA is upregulated in both, the light damaged and the degenerative retina of the rd1 mouse. This common answer to probably different apoptotic stimuli suggests a prominent role for Jak3 in the damaged retina and could therefore be interesting for further investigations.

摘要

视网膜退行性疾病是人类严重视力损害或失明的主要原因。为了开发治疗策略,了解疾病进展过程中发生的分子机制尤为重要。Janus 激酶/信号转导和转录激活因子(Jak/STAT)信号通路的基因和蛋白已被证明在视网膜变性(RD)模型中发挥重要作用。在这里,我们研究了 Jak/STAT 通路中参与的其他基因在诱导(光照)和遗传性(rd1 小鼠)RD 模型中的表达。我们表明,STAT mRNAs 以及 Jak2/shp-1 通路在两种模型中存在差异调节。相比之下,我们表明 Jak3 mRNA 在光损伤和 rd1 小鼠变性视网膜中均上调。这种对可能不同凋亡刺激的共同反应表明 Jak3 在受损视网膜中具有重要作用,因此可能是进一步研究的有趣目标。

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