Plum J, De Smedt M, Leclercq G, Taghon T, Kerre T, Vandekerckhove B
Department of Clinical Chemistry, Microbiology and Immunology, Ghent University Hospital, Ghent University, De Pintelaan 185, 4 Blok A, 9000, Ghent, Belgium.
Semin Immunopathol. 2008 Dec;30(4):411-23. doi: 10.1007/s00281-008-0135-2. Epub 2008 Oct 17.
Human T lymphocytes can be generated from CD34 progenitor cells from different sources. This can be obtained in an in vivo model wherein human thymic tissue and fetal liver is transplanted in an immunodeficient mouse. However, human T cells are also generated in immunodeficient mice without co-transplantation of human thymus or in in vitro hybrid human-mouse fetal thymus organ culture. This shows that xenogeneic mouse thymus tissue supports human T cell differentiation. Finally, human T cells are generated on co-culture with murine stromal cells that express the Delta-like1 ligand for the Notch receptor. How these different environments influence the human T cell repertoire is reviewed and discussed.
人T淋巴细胞可由不同来源的CD34祖细胞产生。这可以在一种体内模型中实现,即将人胸腺组织和胎儿肝脏移植到免疫缺陷小鼠体内。然而,在没有共同移植人胸腺的免疫缺陷小鼠中,或者在体外人-小鼠胎儿胸腺器官共培养中,也能产生人T细胞。这表明异种小鼠胸腺组织支持人T细胞分化。最后,在与表达Notch受体的Delta样1配体的鼠基质细胞共培养时,可产生人T细胞。本文对这些不同环境如何影响人T细胞库进行了综述和讨论。