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Immunology. 1985 Feb;54(2):233-40.
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引用本文的文献

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Immunology. 1988 Feb;63(2):213-7.

本文引用的文献

1
B-cell subpopulations identified by two-colour fluorescence analysis.通过双色荧光分析鉴定的B细胞亚群。
Nature. 1982 Jun 17;297(5867):589-91. doi: 10.1038/297589a0.
2
B cell subpopulations in the mouse: analysis with monoclonal antibodies NIM-R2 and NIM-R3.小鼠中的B细胞亚群:用单克隆抗体NIM-R2和NIM-R3进行分析。
Eur J Immunol. 1982 Sep;12(9):725-32. doi: 10.1002/eji.1830120906.
3
Functional subsets of B cells defined by quantitative differences in surface I-A.由表面I-A定量差异所定义的B细胞功能亚群。
J Immunol. 1981 Jun;126(6):2419-23.
4
B cell differentiation antigens as probes for functional B cell subsets.作为功能性B细胞亚群探针的B细胞分化抗原
Immunol Rev. 1982;64:57-79. doi: 10.1111/j.1600-065x.1982.tb00418.x.
5
Stimulation of murine B cells with anti-Ig antibodies: dominance of a negative signal mediated by the Fc receptor.用抗免疫球蛋白抗体刺激小鼠B细胞:Fc受体介导的负信号占主导地位。
Eur J Immunol. 1980 Sep;10(9):726-9. doi: 10.1002/eji.1830100914.
6
Ly-1 B cells: functionally distinct lymphocytes that secrete IgM autoantibodies.Ly-1 B细胞:分泌IgM自身抗体的功能独特的淋巴细胞。
Proc Natl Acad Sci U S A. 1984 Apr;81(8):2494-8. doi: 10.1073/pnas.81.8.2494.
7
Ia antigens as restriction molecules in Ir-gene controlled T-cell proliferation.Ia抗原作为Ir基因控制的T细胞增殖中的限制分子。
Immunol Rev. 1981;60:59-83. doi: 10.1111/j.1600-065x.1981.tb00362.x.
8
Functional significance of the regulation of macrophage Ia expression.巨噬细胞Ia表达调控的功能意义。
Eur J Immunol. 1984 Feb;14(2):138-43. doi: 10.1002/eji.1830140207.
9
Fc-dependent inhibition of mouse B cell activation by whole anti-mu antibodies.全抗μ抗体对小鼠B细胞活化的Fc依赖性抑制作用。
J Immunol. 1983 Feb;130(2):602-6.
10
The expression of surface IgD on B cells responsive to thymus-independent and thymus-dependent antigens and its requirement for B-cell triggering.对非胸腺依赖性抗原和胸腺依赖性抗原产生反应的B细胞表面IgD的表达及其对B细胞触发的需求。
Immunology. 1983 Feb;48(2):393-400.

与小鼠B细胞膜免疫球蛋白、Fc受体和Ia定量分布相关的功能差异。

Functional differences associated with quantitative distribution of membrane immunoglobulin, Fc receptors and Ia on mouse B cells.

作者信息

Andrew E M, Mackenzie N M, Parkhouse R M

出版信息

Immunology. 1985 Feb;54(2):233-40.

PMID:3881338
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1453500/
Abstract

Murine splenic B cells were stained with antibodies against mIg, Ia or FcR and then separated on the fluorescence-activated cell sorter on the basis of quantitative differences in marker expression; that is, they were fractionated into subpopulations bearing high or low densities of the marker. The separated cells were then tested for their relative capacities for T-dependent primary and secondary antibody responses, and for lipopolysaccharide responsiveness. There was no association between the surface density of any of these markers and the ability of the cells to proliferate in response to lipopolysaccharide. However, a high level of surface Ia was associated with good primary and secondary T-dependent responses. The density of mIg or of FcR showed no association with the capacity for primary responses, but a low density of these two markers, especially FcR, was correlated with good secondary responsiveness. Thus, subpopulations of B cells selected on the basis of quantitative levels of membrane markers can also be distinguished by their functional properties.

摘要

用抗mIg、Ia或FcR抗体对小鼠脾脏B细胞进行染色,然后根据标记物表达的定量差异在荧光激活细胞分选仪上进行分离;也就是说,它们被分成具有高或低密度标记物的亚群。然后测试分离的细胞对T细胞依赖性初次和二次抗体反应以及对脂多糖反应性的相对能力。这些标记物中任何一种的表面密度与细胞对脂多糖反应而增殖的能力之间均无关联。然而,高水平的表面Ia与良好的初次和二次T细胞依赖性反应相关。mIg或FcR的密度与初次反应能力无关,但这两种标记物的低密度,尤其是FcR的低密度,与良好的二次反应性相关。因此,根据膜标记物定量水平选择的B细胞亚群也可以通过其功能特性来区分。