期刊
EXPERIMENTAL HEMATOLOGY
卷 36, 期 8, 页码 1004-1013出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.exphem.2008.03.008
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-
资金
- NHLBI NIH HHS [R01 HL058734, HL46557, R01 HL046557] Funding Source: Medline
Objective. alpha 4 Integrins are major players in lymphoid cell trafficking and immune responses. However, their importance in lymphoid reconstitution and function, studied by antibody blockade or in genetic models of chimeric animals with alpha 4(KO) embryonic stem (ES) cells, competitive repopulation experiments with fetal liver(KO) cells, or in beta 1/beta 7 doubly-deficient mice has yielded disparate conclusions. Materials and Methods. To study the role of alpha 4 integrin (alpha 4,beta 1, alpha 4 beta 7) during adult life, we transplanted lethally irradiated Rag2(-/-) mice with alpha 4(Delta/Delta) or alpha 4(f/f) adult bone marrow (BM) cells and evaluated recipients at several points after transplantation. Results. Lymphomyeloid repopulation (8 months later) was entirely donor-derived in all recipients, and novel insights regarding lymphoid reconstitution and function were revealed. Thymic repopulation was impaired in all alpha 4(Delta/Delta) recipients, likely because of homing defects of BM-derived progenitors, although a role of alpha 4 integrin in intrathymic expansion/maturation of T cells cannot be excluded; reconstitution of gut lymphoid tissue was also greatly diminished because of homing defects of alpha 4(Delta/Delta) cells; impaired immunoglobulin (Ig) M and IgE, but normal IgG responses were seen, suggesting compromised initial B-/T-cell interactions, whereas interferon-gamma production from ovalbumin-stimulated cells was increased, possibly reflecting a bias against Th2 stimulation. Conclusion. These data complement previous observations by defending the role of alpha 4 integrin in thymic and gut lymphoid tissue homing, and by strengthening evidence of attenuated B-cell responses in alpha 4-deficient mice. (c) 2008 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc.
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