B-1 B Cell Development in the Fetus and Adult

被引:257
|
作者
Montecino-Rodriguez, Encarnacion [1 ]
Dorshkind, Kenneth [1 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
关键词
HEMATOPOIETIC STEM-CELLS; ACUTE LYMPHOBLASTIC-LEUKEMIA; COMMON LYMPHOID PROGENITORS; MOUSE BONE-MARROW; YOLK-SAC; DEVELOPMENT PATHWAYS; BLOOD PROGENITORS; HUMAN EQUIVALENT; PRO-B; FETAL;
D O I
10.1016/j.immuni.2011.11.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:13 / 21
页数:9
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