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Publication : B-cell deficiency and reduced B-cell reconstitution in hemoglobin-deficit mice.

First Author  Lipovsky K Year  2003
Journal  Exp Hematol Volume  31
Issue  12 Pages  1230-6
PubMed ID  14662329 Mgi Jnum  J:115668
Mgi Id  MGI:3692055 Doi  10.1016/j.exphem.2003.08.007
Citation  Lipovsky K, et al. (2003) B-cell deficiency and reduced B-cell reconstitution in hemoglobin-deficit mice. Exp Hematol 31(12):1230-6
abstractText  OBJECTIVE: To study the effect of persistent hemoglobin-deficit mutation (hbd/hbd) on hematopoiesis and the function of hematopoietic stem cells (HSCs). METHODS: Young and old mice homozygous for the spontaneous hbd/hbd mutation were compared to young and old wild-type control mice, all on the C57BL/6 background, over cellular composition in blood and bone marrow (BM) using cell counting, complete blood counts, and flow cytometry. BM cells from hbd/hbd mutants and normal controls were also tested for HSC engraftment in vivo using the competitive repopulation assay. RESULTS: Both young and old hbd/hbd mutants exhibited a microcytic anemia with significantly (p<0.01) lower levels of hemoglobin and mean corpuscular volume. There were significant declines in CD45R+ B cells in both blood (p<0.01) and BM (p<0.05) in old hbd/hbd mice, suggesting that B-cell homeostasis was compromised. Total BM cells per mouse was significantly increased (p<0.05) in old hbd/hbd mice. In the competitive repopulation assay in vivo, BM cells from old hbd/hbd donors showed slightly decreased contribution to T cells and myeloid cells but a significantly (p<0.01) decreased engraftment in B lymphocytes, indicating that B-cell hematopoiesis was compromised in old hbd/hbd mice. These data differ from results previously obtained from normal C57BL/6 mice in which BM cell engraftment ability does not decrease with donor age. CONCLUSION: Persistent hbd/hbd mutation causes hematopoiesis defects in the B cell lineage.
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