Choi E Y, Bae Y, Lee D S, Park S H
Department of Pathology, Institute of Allergy and Clinical Immunology, Seoul, Korea.
Cell Mol Biol (Noisy-le-grand). 2001 Feb;47(1):135-43.
During thymic development, immature thymocytes are selected through the interaction with self peptides loaded on self MHC molecules. Although there is a great deal of debates on how specifically thymocytes recognize self peptides during thymic selection, recent data suggest an important role of peptide diversity in selecting an adequate T-cell repertoire in the thymus. The findings that human T-cells, unlike mouse T-cells, express MHC class II molecules on their surfaces and can play as antigen presenting cells suggesting possible peripheral T-T interaction network has not been intensively studied so far. However, the facts that human thymocytes have surface expression of MHC class II molecules and thymocytes can be selected by thymocytes in in vitro re-aggregation culture system led us to propose a novel hypothesis - "T-T interaction during thymic selection". Our proposition is that peripheral T-T interaction through TCR-derived peptides might reflect the selection process in the thymus and that T-T interaction also plays an important role in thymic selection. This review deals with our thymic T-T interaction hypothesis and its implications on human T-cell development.
在胸腺发育过程中,未成熟胸腺细胞通过与加载在自身MHC分子上的自身肽相互作用而被选择。尽管关于胸腺细胞在胸腺选择过程中如何特异性识别自身肽存在大量争论,但最近的数据表明肽多样性在胸腺中选择合适的T细胞库方面具有重要作用。与小鼠T细胞不同,人类T细胞在其表面表达MHC II类分子并可作为抗原呈递细胞,这一发现提示可能存在外周T-T相互作用网络,但迄今为止尚未对此进行深入研究。然而,人类胸腺细胞具有MHC II类分子的表面表达,并且在体外重聚集培养系统中胸腺细胞可被胸腺细胞选择,这些事实促使我们提出一个新的假说——“胸腺选择过程中的T-T相互作用”。我们的观点是,通过TCR衍生肽的外周T-T相互作用可能反映胸腺中的选择过程,并且T-T相互作用在胸腺选择中也起着重要作用。本综述探讨了我们的胸腺T-T相互作用假说及其对人类T细胞发育的影响。