Changing partners at the dance: Variations in STAT concentrations for shaping cytokine function and immune responses to viral infections.

JAK-STAT Pub Date : 2013-01-01 DOI:10.4161/jkst.23504
Lara E Kallal, Christine A Biron
{"title":"Changing partners at the dance: Variations in STAT concentrations for shaping cytokine function and immune responses to viral infections.","authors":"Lara E Kallal,&nbsp;Christine A Biron","doi":"10.4161/jkst.23504","DOIUrl":null,"url":null,"abstract":"<p><p>Differential use of cellular and molecular components shapes immune responses, but understanding of how these are regulated to promote defense and health during infections is still incomplete. Examples include signaling from members of the Janus activated kinase-signal transducer and activator of transcription (JAK-STAT) cytokine family. Following receptor stimulation, individual JAK-STAT cytokines have preferences for particular key STAT molecules to lead to specific cellular responses. Certain of these cytokines, however, can conditionally activate alternative STATs as well as elicit pleiotropic and paradoxical effects. Studies examining basal and infection conditions are revealing intrinsic and induced cellular differences in various intracellular STAT concentrations to control the biological consequences of cytokine exposure. The system can be likened to changing partners at a dance based on competition and relative availability, and sets a framework for understanding the particular conditions promoting subset biological functions of cytokines as needed during evolving immune responses to infections. </p>","PeriodicalId":89791,"journal":{"name":"JAK-STAT","volume":"2 1","pages":"e23504"},"PeriodicalIF":0.0000,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4161/jkst.23504","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JAK-STAT","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4161/jkst.23504","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9

Abstract

Differential use of cellular and molecular components shapes immune responses, but understanding of how these are regulated to promote defense and health during infections is still incomplete. Examples include signaling from members of the Janus activated kinase-signal transducer and activator of transcription (JAK-STAT) cytokine family. Following receptor stimulation, individual JAK-STAT cytokines have preferences for particular key STAT molecules to lead to specific cellular responses. Certain of these cytokines, however, can conditionally activate alternative STATs as well as elicit pleiotropic and paradoxical effects. Studies examining basal and infection conditions are revealing intrinsic and induced cellular differences in various intracellular STAT concentrations to control the biological consequences of cytokine exposure. The system can be likened to changing partners at a dance based on competition and relative availability, and sets a framework for understanding the particular conditions promoting subset biological functions of cytokines as needed during evolving immune responses to infections.

Abstract Image

Abstract Image

Abstract Image

跳舞时改变舞伴:STAT浓度的变化对细胞因子功能的影响和对病毒感染的免疫反应。
细胞和分子成分的不同使用形成了免疫反应,但对这些成分如何在感染期间被调节以促进防御和健康的理解仍然不完整。例子包括Janus活化激酶-信号转换器和转录激活因子(JAK-STAT)细胞因子家族成员的信号传导。在受体刺激后,个体JAK-STAT细胞因子对特定关键STAT分子有偏好,从而导致特定的细胞反应。然而,这些细胞因子中的某些可以有条件地激活替代stat,并引发多效性和矛盾效应。检查基础和感染条件的研究揭示了各种细胞内STAT浓度的内在和诱导细胞差异,以控制细胞因子暴露的生物学后果。该系统可以被比作在竞争和相对可用性的基础上改变舞伴,并为理解在进化免疫反应感染过程中促进细胞因子亚群生物学功能的特定条件设置了框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书