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PMID: 8350062 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The regulated expression of B lineage associated genes during B cell differentiation in bone marrow and fetal liver.

The Journal of experimental medicine ·Vol. 178 ·No. 3 ·1993-09-01 ·Pages 951-60

Li YS, Hayakawa K, Hardy RR

Abstract

The expression of B lineage associated genes during early B cell differentiation stages is not firmly established. Using cell surface markers and multiparameter flow cytometry, bone marrow (BM) cells can be resolved into six fractions, representing sequential stages of development; i.e., pre-Pro-B, early Pro-B, late Pro-B/large Pre-B, small Pre-B, immature B, and mature B cells. Here we quantitate the levels of several B lineage associated genes in each of these fractions by RT-PCR, demonstrating different patterns of expression. We find that expression of terminal deoxynucleotidyl transferase (TdT), lambda 5, and VpreB is predominantly restricted to the Pro-B stages. Rag-1 and Rag-2 expression is also tightly regulated, and is found largely in the Pro-B through small Pre-B stages. Mb-1 is present from Pro-B throughout the pathway at high levels. Finally, Bcl-2 is expressed at high levels only at the pre-Pro-B and mature B stages, whereas it is low during all the intermediate stages. We also correlate this expression data with an analysis of the onset of Ig gene rearrangement as assessed by amplifying D-JH, VH-DJH, and VK-JK. Finally, we report differences in gene expression during B lymphopoiesis at two distinct ontogenic timings, in fetal liver and adult BM: both TdT and the precursor lymphocyte regulated myosin-like light chain are expressed at high levels in the Pro-B cell stage in bone marrow, but are absent from the corresponding fraction in fetal liver. In contrast, lambda 5, VpreB, Rag-1, and Rag-2 are expressed at comparable levels.

Related Genes
MeSH Terms
Animals Antigens, CD B-Lymphocytes/cytology,physiology Base Sequence Bone Marrow Cells CD79 Antigens Cell Differentiation DNA Nucleotidylexotransferase/genetics DNA-Binding Proteins Female Gene Expression Regulation Gene Rearrangement, B-Lymphocyte Genes, Immunoglobulin Hematopoiesis Homeodomain Proteins Liver/embryology Membrane Glycoproteins/genetics Mice Mice, Inbred BALB C Molecular Sequence Data Oligodeoxyribonucleotides/chemistry Proteins/genetics Proto-Oncogene Proteins/genetics Proto-Oncogene Proteins c-bcl-2 RNA, Messenger/genetics Receptors, Antigen, B-Cell/genetics
Chemicals
Antigens, CD CD79 Antigens Cd79a protein, mouse DNA-Binding Proteins Homeodomain Proteins Membrane Glycoproteins Oligodeoxyribonucleotides Proteins Proto-Oncogene Proteins Proto-Oncogene Proteins c-bcl-2 RNA, Messenger Rag2 protein, mouse Receptors, Antigen, B-Cell V(D)J recombination activating protein 2 RAG-1 protein DNA Nucleotidylexotransferase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Li Y S
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
Hayakawa K
Hardy R R
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50 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1993-09-01
Pages
951-60
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2191150
Subset
IM
Grants
NIAID NIH HHS · AI-26782 · United States
NCI NIH HHS · CA-06927 · United States
NCRR NIH HHS · RR-05539 · United States
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