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辅助性T细胞分化:反复无常。

T helper cell differentiation: on again, off again.

作者信息

Grogan Jane L, Locksley Richard M

机构信息

Howard Hughes Medical Institute, University of California San Francisco, 521 Parnassus Avenue, C-443, San Francisco, CA 94143-0654, USA.

出版信息

Curr Opin Immunol. 2002 Jun;14(3):366-72. doi: 10.1016/s0952-7915(02)00340-0.

Abstract

Recent studies raise the possibility that T helper (Th) polarization may be attributable to generalized activation and regulated silencing rather than regulated activation of target cytokine genes. The binding of transcription factors GATA-3 or T-bet to specific enhancers does recruit transcription factors such as NFAT-1 to IL-4 or IFNgamma promoters, respectively; however, GATA-3 also intrinsically suppresses T-bet and vice versa. Silencing of GATA-3/T-bet, which is influenced by factors such as cytokines, is associated with irreversible Th polarization. For the first few divisions (perhaps reflecting the situation in lymph nodes), naive Th cells retain pluripotency; after further cell divisions (perhaps under the influence of an inflammatory cytokine milieu) they may become polarized appropriately to respond to the specific environment.

摘要

最近的研究提出了一种可能性,即辅助性T细胞(Th)极化可能归因于普遍激活和调控性沉默,而非靶细胞因子基因的调控性激活。转录因子GATA-3或T-bet与特定增强子的结合确实分别将诸如NFAT-1等转录因子募集至IL-4或IFNγ启动子;然而,GATA-3也内在地抑制T-bet,反之亦然。受细胞因子等因素影响的GATA-3/T-bet沉默与不可逆的Th极化相关。在最初的几次分裂中(可能反映淋巴结中的情况),初始Th细胞保持多能性;在进一步的细胞分裂后(可能受炎性细胞因子环境的影响),它们可能会适当地极化以响应特定环境。

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