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PMID: 1827140 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Resolution and characterization of pro-B and pre-pro-B cell stages in normal mouse bone marrow.

The Journal of experimental medicine ·Vol. 173 ·No. 5 ·1991-05-01 ·Pages 1213-25

Hardy RR, Carmack CE, Shinton SA, Kemp JD, Hayakawa K

Abstract

We have resolved B220+ IgM- B-lineage cells in mouse bone marrow into four fractions based on differential cell surface expression of determinants recognized by S7 (leukosialin, CD43), BP-1, and 30F1 (heat stable antigen). Functional differences among these fractions can be correlated with Ig gene rearrangement status. The largest fraction, lacking S7, consists of pre-B cells whereas the others, expressing S7, include B lineage cells before pre-B. These S7+ fractions, provisionally termed Fr. A, Fr. B, and Fr. C, can differentiate in a stromal layer culture system. Phenotypic alteration during such culture suggests an ordering of these stages from Fr. A to Fr. B to Fr. C and thence to S7- pre-B cells. Using polymerase chain reaction amplification with pairs of oligonucleotide primers for regions 5' of JH1, DFL16.1, and Jk1, we find that the Ig genes of Fr. A are in germline configuration, whereas Fr. B and C are pro-B cell stages with increasing D-J rearrangement, but no V-D-J. Finally, functional analysis demonstrates that the proliferative response to IL-7, an early B lineage growth factor, is restricted to S7+ stages and, furthermore, that an additional, cell contact-mediated signal is essential for survival of Fr. A.

MeSH Terms
Animals Antigens, CD Antigens, Surface/genetics,immunology,metabolism B-Lymphocytes/cytology,immunology,metabolism Base Sequence Biotin/metabolism Bone Marrow/immunology,metabolism Bone Marrow Cells Cell Differentiation/physiology Cell Membrane/metabolism,ultrastructure Cells, Cultured DNA/analysis,genetics Female Gene Rearrangement, B-Lymphocyte, Heavy Chain/genetics,immunology Gene Rearrangement, B-Lymphocyte, Light Chain/genetics,immunology Hematopoietic Stem Cells/cytology,immunology,metabolism Immunoglobulin Heavy Chains/genetics,immunology,metabolism Leukosialin Mice Molecular Sequence Data Peptide Fragments/genetics,immunology,metabolism Phenotype Phycoerythrin/metabolism Polymerase Chain Reaction Sialoglycoproteins/metabolism
Chemicals
Antigens, CD Antigens, Surface Immunoglobulin Heavy Chains Leukosialin Peptide Fragments Sialoglycoproteins Spn protein, mouse Phycoerythrin Biotin DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hardy R R
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
Carmack C E
Shinton S A
Kemp J D
Hayakawa K
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1991-05-01
Pages
1213-25
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2118850
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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