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Transitional B cell subsets in human bone marrow
Author(s) -
Agrawal S.,
Smith S. A. B. C.,
Tangye S. G.,
Sewell W. A.
Publication year - 2013
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/cei.12149
Subject(s) - bone marrow , immunoglobulin d , cd19 , cd38 , b cell , transitional cell , immunology , biology , b 1 cell , flow cytometry , pathology , microbiology and biotechnology , medicine , antibody , t cell , stem cell , antigen presenting cell , cd34 , immune system , transitional cell carcinoma , bladder cancer , cancer
Summary B cells originate from precursors in the bone marrow, and the first cells which migrate to the peripheral blood have been classified as ‘transitional B cells’. Transitional B cells have been characterized in human blood with stage 1 ( T 1) and stage 2 ( T 2) subsets being proposed. In the present study, 27 normal human bone marrow samples were analysed for transitional B cell markers by eight‐colour flow cytometry. T 1 transitional B cells ( CD 45 + CD 19 + CD 10 + IgM + IgD lo ) and T 2 transitional B cells ( CD 45 + CD 19 + CD 10 + IgM + IgD + ) were identified in normal bone marrow samples at a mean frequency of 3·2 and 3·1% of total B lineage cells, respectively. A majority of the bone marrow transitional B cells were CD 24 hi CD 38 hi , the phenotype of blood transitional B cells. Consistent with recent peripheral blood data, T 2 B cells had a significantly higher CD 21 expression compared with T 1 B cells (72·4 versus 40·9%) in the bone marrow. These data raise the possibility that transitional B cells are capable of differentiating from T 1 to T 2 B cells within the bone marrow. Furthermore, transitional cells at either stages 1 or 2 might be capable of migrating out of the bone marrow.

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