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Title: Effect of hemopoietic microenvironment on splenic suppressor macrophages in congenitally anemic mice of genotype S1/sup d/

Technical Report ·
OSTI ID:5803971

Mechanisms underlying mononuclear phagocyte specialization are being probed by studying suppressor macrophages as a reference population in mouse models with impaired blood monocyte formation. Splenic suppressor macrophages, defined by PGE-mediated inhibition of Con A-induced T lymphocyte proliferation are induced by the i.p. administration of Corynebacterium parvum (CP). Mice severely depleted of bone marrow and blood monocytes by treatment with /sup 89/Sr fail to show this suppressor macrophages response to CP, although macrophages-forming stem cells, assessed as splenic M-CFC in vitro, are increased 20-fold. These observations suggest that radiosensitive bone marrow stem cells are necessary for the generation of both suppressor macrophages and monocytes and that one such stem cell may be common to both types of mononuclear phagocytes. This notion was explored further by employing congenitally anemic mice of the genotype S1/S1 superscript d in which the hemopoietic microenvironment is genetically defective and thus unable to support the proliferation, differentiation, and function of stem cells. The congenital defect was found to be additionally expressed in the S1/S1/sup d/ mouse by a monocytopenia of less than 10% of the values in normal congenic littermate controls and by the failure of splenic M-CFC to increase in response to cp. PGE-producing suppressor macrophages expressing Fcy2b receptors, however, were induced by CP in S1/S1/sup d/ mice with no significant diminution of suppressor activity.

Research Organization:
Medical Coll. of Pennsylvania, Philadelphia (USA). Dept. of Microbiology and Immunology
OSTI ID:
5803971
Report Number(s):
AD-A-165525/7/XAB
Country of Publication:
United States
Language:
English

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