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从体外分化的胚胎干细胞诱导T细胞发育并建立T细胞功能。

Induction of T cell development and establishment of T cell competence from embryonic stem cells differentiated in vitro.

作者信息

Schmitt Thomas M, de Pooter Renée F, Gronski Matthew A, Cho Sarah K, Ohashi Pamela S, Zúñiga-Pflücker Juan Carlos

机构信息

Department of Immunology, University of Toronto, Sunnybrook and Women's College Health Sciences Centre, 2075 Bayview Avenue, Toronto, Ontario, M4N 3M5 Canada.

出版信息

Nat Immunol. 2004 Apr;5(4):410-7. doi: 10.1038/ni1055. Epub 2004 Mar 21.

Abstract

Embryonic stem cells (ESCs) have the potential to serve as a renewable source of transplantable tissue-specific stem cells. However, the molecular cues necessary to direct the differentiation of ESCs toward specific cell lineages remain obscure. Here we report the successful induction of ESC differentiation into mature functional T lymphocytes with a simple in vitro coculture system. The directed differentiation of ESCs into T cells required the engagement of Notch receptors by Delta-like 1 ligand (DL1) expressed on the OP9-DL1 stromal cell line. We found a normal program of T cell differentiation in ESC-OP9-DL1 cell cocultures. ESC-derived T cell progenitors effectively reconstituted the T cell compartment of immunodeficient mice, enabling an effective response to a viral infection. These findings provide a powerful tool for the molecular analysis of T cell development and open new avenues for the development of immunotherapeutic approaches using defined sources of stem cells.

摘要

胚胎干细胞(ESCs)有潜力成为可移植的组织特异性干细胞的可再生来源。然而,指导胚胎干细胞向特定细胞谱系分化所需的分子信号仍不清楚。在此,我们报告了利用一种简单的体外共培养系统成功将胚胎干细胞诱导分化为成熟的功能性T淋巴细胞。胚胎干细胞向T细胞的定向分化需要OP9-DL1基质细胞系表达的Delta样1配体(DL1)与Notch受体结合。我们在胚胎干细胞-OP9-DL1细胞共培养物中发现了正常的T细胞分化程序。胚胎干细胞来源的T细胞祖细胞有效地重建了免疫缺陷小鼠的T细胞区室,使其能够对病毒感染产生有效反应。这些发现为T细胞发育的分子分析提供了一个强大的工具,并为利用特定来源的干细胞开发免疫治疗方法开辟了新途径。

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