Kawamoto H, Ohmura K, Katsura Y
Department of Immunology, Institute for Frontier Medical Sciences, Kyoto University, Japan.
J Immunol. 1998 Oct 15;161(8):3799-802.
The most immature population of fetal thymus (FT) cells has been shown to generate not only T but also B and myeloid cells. The present study was undertaken to clarify whether such a multipotent activity of the earliest population of FT cells is attributed to multipotent hemopoietic progenitors or to a mixture of lineage-restricted progenitors. Examination of individual FT progenitors by a recently established clonal assay system, which is able to determine the developmental potential of each progenitor toward T, B, and myeloid lineages, elucidated that a large majority of progenitors in FT were restricted to the T cell lineage. Presence of a small number of B or myeloid lineage-restricted progenitors was also disclosed. No multipotent progenitors, however, were detected in FT. These results are consistent with our recent finding that restriction of hemopoietic stem cells to T, B, and myeloid lineages takes place in the fetal liver.
已证明胎儿胸腺(FT)中最不成熟的细胞群不仅能产生T细胞,还能产生B细胞和髓系细胞。本研究旨在阐明FT细胞最早期群体的这种多能活性是归因于多能造血祖细胞还是谱系受限祖细胞的混合物。通过最近建立的克隆分析系统对单个FT祖细胞进行检测,该系统能够确定每个祖细胞向T、B和髓系谱系的发育潜能,结果表明FT中的大多数祖细胞仅限于T细胞谱系。还发现了少数B或髓系谱系受限的祖细胞。然而,在FT中未检测到多能祖细胞。这些结果与我们最近的发现一致,即造血干细胞在胎儿肝脏中向T、B和髓系谱系的分化发生。