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体内 T 淋巴细胞和 T 细胞前体运输、扩增和激活的同时可视化。

Concurrent visualization of trafficking, expansion, and activation of T lymphocytes and T-cell precursors in vivo.

机构信息

Department of Immunology, Memorial Sloan-Kettering Cancer Center, New York, NY;

出版信息

Blood. 2010 Sep 16;116(11):e18-25. doi: 10.1182/blood-2009-12-259432. Epub 2010 May 28.

Abstract

We have developed a dual bioluminescent reporter system allowing noninvasive, concomitant imaging of T-cell trafficking, expansion, and activation of nuclear factor of activated T cells (NFAT) in vivo. NFAT activation plays an important role in T-cell activation and T-cell development. Therefore we used this system to determine spatial-temporal activation patterns of (1) proliferating T lymphocytes during graft-versus-host disease (GVHD) and (2) T-cell precursors during T-cell development after allogeneic hematopoietic stem cell transplantation (HSCT). In the first days after HSCT, donor T cells migrated to the peripheral lymph nodes and the intestines, whereas the NFAT activation was dominant in the intestines, suggesting an important role for the intestines in the early stages of alloactivation during development of GVHD. After adoptive transfer of in vitro-derived T-cell receptor (TCR) H-Y transgenic T-cell precursors into B6 (H-2(b)) hosts of both sexes, NFAT signaling and development into CD4(+) or CD8(+) single-positive cells could only be detected in the thymus of female recipients indicating either absence of positive selection or prompt depletion of double-positive thymocytes in the male recipients. Because NFAT plays an important role in a wide range of cell types, our system could provide new insights into a variety of biologic processes.

摘要

我们开发了一种双发光报告系统,允许非侵入性地同时对体内 T 细胞的迁移、增殖和 T 细胞激活因子(NFAT)的激活进行成像。NFAT 的激活在 T 细胞的激活和发育中起着重要作用。因此,我们使用该系统来确定(1)移植物抗宿主病(GVHD)期间增殖的 T 淋巴细胞和(2)异基因造血干细胞移植(HSCT)后 T 细胞发育期间 T 细胞前体的时空激活模式。在 HSCT 后的最初几天,供体 T 细胞迁移到外周淋巴结和肠道,而 NFAT 的激活在肠道中占主导地位,这表明肠道在 GVHD 发展过程中的同种异体激活的早期阶段发挥着重要作用。在将体外衍生的 TCR H-Y 转基因 T 细胞前体过继转移到 B6(H-2(b))的雄性和雌性宿主后,仅在雌性受体的胸腺中可以检测到 NFAT 信号和向 CD4(+)或 CD8(+)单阳性细胞的发育,这表明在雄性受体中不存在阳性选择或双阳性胸腺细胞的迅速耗竭。由于 NFAT 在广泛的细胞类型中发挥着重要作用,我们的系统可以为多种生物学过程提供新的见解。

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