Literature DB >> 15350509

Optimal timing to repopulation of resident alveolar macrophages with donor cells following total body irradiation and bone marrow transplantation in mice.

Gustavo Matute-Bello1, Janet S Lee, Charles W Frevert, W Conrad Liles, Steven Sutlief, Kimberly Ballman, Venus Wong, Amy Selk, Thomas R Martin.   

Abstract

To determine the time required to repopulate mouse lungs with donor alveolar macrophages following total body irradiation (TBI) and bone marrow transplantation (BMT), C57Bl/6 mice were subjected to TBI with 900 cGy, followed by transplantation of bone marrow cells from mice expressing green fluorescent protein (GFP) in their somatic cells. The mice were euthanized at either 30 (n=5), 60 (n=5) or 90 (n=5) days following BMT. Thirty days following transplantation, 87.8 +/- 3.9% (mean +/- S.E.M.) circulating leukocytes in recipient mice were derived from the donor, as determined by fluorescence activated cell sorting (FACS) analysis for GFP. However, only 46.9 +/- 7.4% of the resident alveolar cells expressed GFP, indicating incomplete repopulation. By day 60 post-transplantation, the percentage of bronchoalveolar lavage fluid (BALF) cells expressing GFP reached 74.5 +/- 2.4%, remaining stable 90 days after transplantation (80.4 +/- 1.9%). We conclude that 60 days after TBI with 900 cGy and bone marrow transplantation, the majority of the lung resident alveolar macrophages is of donor origin. This study provides useful information regarding the time of reconstitution with donor alveolar macrophages in the pulmonary airspaces of recipient mice following marrow transplantation.

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Year:  2004        PMID: 15350509     DOI: 10.1016/j.jim.2004.05.010

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  32 in total

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2.  The Duffy antigen modifies systemic and local tissue chemokine responses following lipopolysaccharide stimulation.

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7.  Comparison of conditioning regimens for alveolar macrophage reconstitution and innate immune function post bone marrow transplant.

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Review 9.  Circulating monocytes: an appropriate model for bone-related study.

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