A defect in inducible beta-galactosidase of B lymphocytes in the osteopetrotic (mi/mi) mouse

被引:11
作者
Yamamoto, N
Naraparaju, VR
机构
[1] Lab. Cancer Immunol. Molec. Biol., Albert Einstein Cancer Center, Philadelphia, PA
[2] Lab. Cancer Immunol. Molec. Biol., Albert Einstein Cancer Center, Korman Research Pavilion B-31, Philadelphia, PA 19141
关键词
D O I
10.1046/j.1365-2567.1996.d01-684.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages were activated by administration of an inflammatory lipid metabolite, lysophosphatidylcholine (lyso-Pc), to wild type mice but not murine (microphthalmic) osteopetrotic (mi/mi) mutant mice. In vitro treatment of wild type mouse peritoneal cells with lyso-Pc efficiently activated macrophages whereas lyso-Pc-treatment of mi mutant mouse peritoneal cells resulted in no activation of macrophages. Generation of macrophage activating factor requires a precursor protein, serum vitamin D binding protein (DBP), and participation of lyso-Pc-inducible beta-galactosidase of B lymphocytes. Lyso-Pc-inducible beta-galactosidase of B lymphocytes was found to be defective in mi mutant mice.
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页码:604 / 610
页数:7
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