Transitional B cell subsets in human bone marrow

Author:

Agrawal S123,Smith S A B C1,Tangye S G23,Sewell W A123

Affiliation:

1. Immunology Department, SydPath, St Vincent's Pathology, St Vincent's Hospital Sydney, NSW, Australia

2. St Vincent's Clinical School, University of NSW, NSW, Australia

3. Garvan Institute of Medical Research, Darlinghurst, NSW, Australia

Abstract

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 (T1) and stage 2 (T2) 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. T1 transitional B cells (CD45+CD19+CD10+IgM+IgDlo) and T2 transitional B cells (CD45+CD19+CD10+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 CD24hiCD38hi, the phenotype of blood transitional B cells. Consistent with recent peripheral blood data, T2 B cells had a significantly higher CD21 expression compared with T1 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 T1 to T2 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.

Funder

St Vincent's Clinical School and the Faculty of Medicine, University of New South Wales

Royal College of Pathologists of Australasia Scholarship for Medical Schools

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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