Mouse bone marrow-derived mast cells and mast cell lines constitutively produce B cell growth and differentiation activities

被引:0
|
作者
Tkaczyk, C [1 ]
Frandji, P [1 ]
Botros, HG [1 ]
Poncet, P [1 ]
Lapeyre, J [1 ]
Peronet, R [1 ]
David, B [1 ]
Mecheri, S [1 ]
机构
[1] INST PASTEUR,UNITE IMMUNOALLERGIE,F-75724 PARIS 15,FRANCE
来源
JOURNAL OF IMMUNOLOGY | 1996年 / 157卷 / 04期
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The present report describes a novel function of mast cells that consists of a B cell growth activity. The B cell response occurred without any stimulation or preactivation of mast cells, A small number of mast cells was required, since mast cell/B cell ratios as low as 1/100 to 1/10,000 lead to effective B cell activation. Mast cell-dependent B cell activation resulted, within 48 h of incubation, in blast formation, proliferation, and IgM production. Both low and high density B cells were responsive to mast cells. Supernatants from unstimulated mast cells could also activate B cells, suggesting that a B cell-stimulating activity (MC-BSA) is mediated by a soluble factor(s), The addition of anti-IL-4 or anti-IL-6 mAbs or even proteases to the mast cell-derived supernatants did not alter B cell activation. However, treatment of mast cells with mitomycin C or actinomycin D, or paraformaldehyde fixation totally abrogated MC-BSA, Fractionation of mast cell supernatant by gel filtration chromatography resulted in four peaks, ranging from >200 to 15 kDa, all of which were biologically active on B cells. Because mast cells are known to continuously release proteoglycans, MC-BSA was subjected to chondroitinase and heparinase treatment, but no significant inhibition of B cell activation was obtained, This direct T cell-independent stimulatory effect of mast cells on B cells could account for a mechanism by which plasma cells are continuously produced in lymphoid organs and particularly in hone marrow.
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页码:1720 / 1728
页数:9
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