B cells are generated from hematopoietic stem cells (HSCs) in the liver during the fetal life, and in the bone marrow in the adult. The differentiation pathway from HSC to mature B cell can be divided into several stages, based on the phenotype and on functional properties that cells of the B lineage progressively acquire. Progenitor B (pro-B) cells can be identified by cell surface expression of B220, CD43, and c-kit. Differential expression of heat-stable antigen (HSA) and of the maturation marker BP-1 discriminates four fractions of pro-B cells (fractions A, B, C, and C′ 1). At this stage of development, DNA rearrangement begins in the Ig H chain locus. Most pro-B cells of fraction A carry Ig genes in germline configuration. DH→JH rearrangements are found in almost all cells of fraction B. VH...
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3 January 2000
Commentary|
January 03 2000
The Development of B Cells in the Bone Marrow Is Controlled by the Balance between Cell-Autonomous Mechanisms and Signals from the Microenvironment
Rita Carsetti
Rita Carsetti
aMax-Planck-Institut für Immunbiologie, Department of Developmental Immunology, D-79108 Freiberg, Germany
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Rita Carsetti
aMax-Planck-Institut für Immunbiologie, Department of Developmental Immunology, D-79108 Freiberg, Germany
Received:
November 23 1999
Accepted:
November 29 1999
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2000 The Rockefeller University Press
2000
The Rockefeller University Press
J Exp Med (2000) 191 (1): 5–8.
Article history
Received:
November 23 1999
Accepted:
November 29 1999
Citation
Rita Carsetti; The Development of B Cells in the Bone Marrow Is Controlled by the Balance between Cell-Autonomous Mechanisms and Signals from the Microenvironment. J Exp Med 3 January 2000; 191 (1): 5–8. doi: https://doi.org/10.1084/jem.191.1.5
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