Jenkinson Eric J, Jenkinson William E, Rossi Simona W, Anderson Graham
MRC Centre for Immune Regulation, Division of Immunity and Infection, Institute for Biomedical Research, Medical School, University of Birmingham, Birmingham B15 2TT, UK.
Nat Rev Immunol. 2006 Jul;6(7):551-5. doi: 10.1038/nri1883.
The current dogma is that the thymus is colonized by progenitors that retain the capacity to generate both T cells and B cells, and that intrathymic Notch signalling determines lineage choice so that T cells, rather than B cells, develop in the thymus. However, evidence is now accumulating to indicate that, at least during fetal life, this is not the case. Rather, it now seems that the fetal thymus is colonized by progenitors that have already made the T-cell versus B-cell lineage choice. We propose an alternative role for Notch signalling in the thymus, which is not to mediate this choice but instead to reveal it by supporting further T-cell differentiation in the thymic microenvironment.
目前的主流观点认为,胸腺由祖细胞定植,这些祖细胞保留了产生T细胞和B细胞的能力,并且胸腺内的Notch信号决定谱系选择,从而使T细胞而非B细胞在胸腺中发育。然而,现在越来越多的证据表明,至少在胎儿期并非如此。相反,现在看来胎儿胸腺是由已经做出T细胞与B细胞谱系选择的祖细胞定植的。我们提出了Notch信号在胸腺中的另一种作用,即它不是介导这种选择,而是通过支持胸腺微环境中T细胞的进一步分化来揭示这种选择。