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STCP-1(MDC)CC趋化因子特异性作用于慢性活化的Th2淋巴细胞,由单核细胞在受到Th2细胞因子IL-4和IL-13刺激时产生。

STCP-1 (MDC) CC chemokine acts specifically on chronically activated Th2 lymphocytes and is produced by monocytes on stimulation with Th2 cytokines IL-4 and IL-13.

作者信息

Andrew D P, Chang M S, McNinch J, Wathen S T, Rihanek M, Tseng J, Spellberg J P, Elias C G

机构信息

Amgen Inc., Boulder, CO 80301, USA.

出版信息

J Immunol. 1998 Nov 1;161(9):5027-38.

PMID:9794440
Abstract

STCP-1 stimulated T cell chemoattractant protein-1 (STCP-1) (macrophage-derived chemokine; MDC), a recently described CC chemokine for chronically activated T lymphocytes, was found to act specifically on a subset of memory CD4 lymphocytes that displayed a Th2 cytokine profile. Also, STCP-1, thymus and activation regulated chemokine (TARC), eotaxin, and eotaxin-2 acted specifically on in vitro derived Th2 lymphocytes, while IP-10 (IFN-gamma-inducible 10-kDa protein) showed some preference for Th1 lymphocytes. The corresponding receptors for eotaxin, TARC, and IP-10 are also differentially expressed on Th1 and Th2 lymphocytes. In desensitization Ca flux experiments, TARC and STCP-1 bound to a common receptor and therefore at least one chemokine receptor for STCP-1 is CCR4. STCP-1 expression is restricted to immune cells. Dendritic cells, B cells, and macrophages produce STCP-1 constitutively, while NK cells, monocytes, and CD4 lymphocytes produce STCP-1 upon appropriate stimulation. Production of STCP-1 is positively modulated by Th2 cytokines IL-4 and IL-13 but inhibited by IL-10.

摘要

STCP-1刺激T细胞趋化蛋白-1(STCP-1)(巨噬细胞衍生趋化因子;MDC),一种最近被描述的针对慢性活化T淋巴细胞的CC趋化因子,被发现特异性作用于显示Th2细胞因子谱的记忆性CD4淋巴细胞亚群。此外,STCP-1、胸腺和活化调节趋化因子(TARC)、嗜酸性粒细胞趋化因子和嗜酸性粒细胞趋化因子-2特异性作用于体外衍生的Th2淋巴细胞,而IP-10(γ干扰素诱导的10 kDa蛋白)对Th1淋巴细胞表现出一定偏好。嗜酸性粒细胞趋化因子、TARC和IP-10的相应受体在Th1和Th2淋巴细胞上也有差异表达。在脱敏钙流实验中,TARC和STCP-1与共同受体结合,因此STCP-1的至少一种趋化因子受体是CCR4。STCP-1的表达局限于免疫细胞。树突状细胞、B细胞和巨噬细胞组成性产生STCP-1,而NK细胞、单核细胞和CD4淋巴细胞在适当刺激后产生STCP-1。STCP-1的产生受到Th2细胞因子IL-4和IL-13的正向调节,但受到IL-10的抑制。

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