Department of Pathology and Laboratory Medicine, The David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
Immunity. 2012 Jan 27;36(1):13-21. doi: 10.1016/j.immuni.2011.11.017.
Models of hematopoiesis often depict lymphocyte production as a uniform process in which a homogenous population of hematopoietic stem cells (HSCs) generates progenitors from which all types of lymphocytes are derived. However, it is increasingly evident that these schemes are too simplistic and that the lymphoid potential of HSCs and precursors arising in the embryo, fetus, neonate, and adult is remarkably distinct. We review recent findings regarding the development of B lymphocytes, and the B-1 B cell lineage in particular, as a case in point. These studies show that B-1 and B-2 B cells involved in innate and adaptive immune responses, respectively, arise in staggered waves of development from distinct progenitors. We discuss the implications of this layered model of B cell development for understanding normal and dysregulated B lymphopoiesis.
造血模型通常将淋巴细胞的产生描述为一个均匀的过程,其中一个同质的造血干细胞 (HSC) 群体产生祖细胞,所有类型的淋巴细胞均由这些祖细胞衍生而来。然而,越来越明显的是,这些方案过于简单化,胚胎、胎儿、新生儿和成人中 HSCs 和前体的淋巴样潜能明显不同。我们回顾了最近关于 B 淋巴细胞发育的发现,特别是 B-1 B 细胞谱系,作为一个典型例子。这些研究表明,分别参与固有和适应性免疫反应的 B-1 和 B-2 B 细胞分别来自不同的祖细胞,以交错的发育波出现。我们讨论了这种分层的 B 细胞发育模型对理解正常和失调的 B 淋巴样发生的意义。