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Generation of functionally distinct B lymphocytes from common myeloid progenitors.
- Source :
-
Clinical and experimental immunology [Clin Exp Immunol] 2007 Nov; Vol. 150 (2), pp. 349-57. Date of Electronic Publication: 2007 Sep 05. - Publication Year :
- 2007
-
Abstract
- Current models of adult haematopoiesis propose that haematopoietic stem cells (HSCs) differentiate into common lymphoid (CLP) and common myeloid (CMP) progenitors and establish an early separation between myeloid and lymphoid lineages. Nevertheless, the developmental potential of CMP-associated B cells suggests the existence of alternate pathways for B lymphopoesis. The aim of this study was to compare the developmental and functional properties of CMP- and CLP-derived B cells. While both populations matured through pro-B cell and transitional B cell intermediates in the bone marrow and spleen, respectively, following transfer into irradiated mice, mature CMP- and CLP-derived B cells exhibit distinct functional responses. Specifically, CMP-derived B cells did not respond to mitogenic stimulation to the same degree as their CLP-derived counterparts and secrete lower levels of IgM and the inflammatory cytokines such as interleukin (IL)-6 and IL-10. Together, these data suggest the existence of multiple pathways for generating functionally distinct B cells from bone marrow precursors.
- Subjects :
- Adoptive Transfer
Animals
Antigens, CD19 analysis
Bone Marrow Cells immunology
Cell Differentiation immunology
Cells, Cultured
Cytokines biosynthesis
Immunoglobulin M biosynthesis
Lymph Nodes immunology
Mice
Mice, Inbred C57BL
Peritoneal Cavity cytology
B-Lymphocyte Subsets immunology
Lymphopoiesis immunology
Myeloid Progenitor Cells cytology
Precursor Cells, B-Lymphoid cytology
Subjects
Details
- Language :
- English
- ISSN :
- 1365-2249
- Volume :
- 150
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Clinical and experimental immunology
- Publication Type :
- Academic Journal
- Accession number :
- 17822442
- Full Text :
- https://doi.org/10.1111/j.1365-2249.2007.03493.x