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免疫谱系中共同γ链细胞因子的交织特征。

The interweaved signatures of common-gamma-chain cytokines across immunologic lineages.

机构信息

Department of Immunology, Harvard Medical School , Boston, MA, USA.

Broad Institute of MIT and Harvard , Cambridge, MA, USA.

出版信息

J Exp Med. 2023 Jul 3;220(7). doi: 10.1084/jem.20222052. Epub 2023 Mar 28.

Abstract

"γc" cytokines are a family whose receptors share a "common-gamma-chain" signaling moiety, and play central roles in differentiation, homeostasis, and communications of all immunocyte lineages. As a resource to better understand their range and specificity of action, we profiled by RNAseq the immediate-early responses to the main γc cytokines across all immunocyte lineages. The results reveal an unprecedented landscape: broader, with extensive overlap between cytokines (one cytokine doing in one cell what another does elsewhere) and essentially no effects unique to any one cytokine. Responses include a major downregulation component and a broad Myc-controlled resetting of biosynthetic and metabolic pathways. Various mechanisms appear involved: fast transcriptional activation, chromatin remodeling, and mRNA destabilization. Other surprises were uncovered: IL2 effects in mast cells, shifts between follicular and marginal zone B cells, paradoxical and cell-specific cross-talk between interferon and γc signatures, or an NKT-like program induced by IL21 in CD8+ T cells.

摘要

"γc"细胞因子家族的受体共享一个"共同γ链"信号部分,在所有免疫细胞谱系的分化、稳态和通讯中发挥核心作用。为了更好地了解它们的作用范围和特异性,我们通过 RNAseq 对所有免疫细胞谱系中主要的 γc 细胞因子的即刻早期反应进行了分析。结果揭示了一个前所未有的景观:更广泛,细胞因子之间有广泛的重叠(一种细胞因子在一种细胞中所做的与另一种细胞在其他地方所做的相同),基本上没有任何一种细胞因子具有独特的作用。反应包括一个主要的下调成分和一个广泛的 Myc 控制的生物合成和代谢途径的重置。涉及到各种机制:快速转录激活、染色质重塑和 mRNA 不稳定性。还发现了其他惊喜:IL2 在肥大细胞中的作用、滤泡和边缘区 B 细胞之间的转变、干扰素和 γc 特征之间的反常和细胞特异性交叉对话,或者 IL21 在 CD8+T 细胞中诱导的类似 NKT 的程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee57/10067526/64b8c48aa5b8/JEM_20222052_Fig1.jpg

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