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信号转导子和转录激活子(STAT)家族成员在寄生虫感染中的作用。

Signal Transducers and Activators of Transcription (STAT) family members in helminth infections.

机构信息

Unidad de Biomedicina, Facultad de Estudios Superiores-Iztacala, Universidad Nacional Autónoma de México-UNAM, México.

出版信息

Int J Biol Sci. 2011;7(9):1371-81. doi: 10.7150/ijbs.7.1371. Epub 2011 Nov 1.

Abstract

Helminth parasites are a diverse group of multicellular organisms. Despite their heterogeneity, helminths share many common characteristics, such as the modulation of the immune system of their hosts towards a permissive state that favors their development. They induce strong Th2-like responses with high levels of IL-4, IL-5 and IL-13 cytokines, and decreased production of proinflammatory cytokines such as IFN-γ. IL-4, IFN-γ and other cytokines bind with their specific cytokine receptors to trigger an immediate signaling pathway in which different tyrosine kinases (e.g. Janus kinases) are involved. Furthermore, a seven-member family of transcription factors named Signal Transducers and Activators of Transcription (STAT) that initiate the transcriptional activation of different genes are also involved and regulate downstream the JAK/STAT signaling pathway. However, how helminths avoid and modulate immune responses remains unclear; moreover, information concerning STAT-mediated immune regulation during helminth infections is scarce. Here, we review the research on mice deficient in STAT molecules, highlighting the importance of the JAK/STAT signaling pathway in regulating susceptibility and/or resistance in these infections.

摘要

寄生虫是一类多样化的多细胞生物。尽管它们具有异质性,但寄生虫有许多共同的特征,例如调节宿主的免疫系统使其处于有利于寄生虫发育的许可状态。它们诱导强烈的 Th2 样反应,产生高水平的白细胞介素-4(IL-4)、白细胞介素-5(IL-5)和白细胞介素-13(IL-13)细胞因子,同时减少促炎细胞因子如干扰素-γ(IFN-γ)的产生。IL-4、IFN-γ 和其他细胞因子与它们特定的细胞因子受体结合,触发一个即时信号通路,其中涉及不同的酪氨酸激酶(如 Janus 激酶)。此外,还涉及一个名为信号转导子和转录激活子(STAT)的七成员转录因子家族,它启动不同基因的转录激活,并调节 JAK/STAT 信号通路的下游。然而,寄生虫如何避免和调节免疫反应仍不清楚;此外,关于 STAT 介导的寄生虫感染期间免疫调节的信息也很缺乏。在这里,我们综述了 STAT 分子缺陷小鼠的研究,强调了 JAK/STAT 信号通路在调节这些感染中的易感性和/或抗性方面的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/126e/3221944/1670077d5ab8/ijbsv07p1371g01.jpg

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