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大型活化B细胞是8-溴鸟苷和8-巯基鸟苷的主要B细胞靶点。

Large, activated B cells are the primary B-cell target of 8-bromoguanosine and 8-mercaptoguanosine.

作者信息

Wicker L S, Boltz R C, Nichols E A, Miller B J, Sigal N H, Peterson L B

出版信息

Cell Immunol. 1987 May;106(2):318-29. doi: 10.1016/0008-8749(87)90175-4.

Abstract

Previous studies have documented the ability of 8-bromoguanosine (8-BrGuo) and 8-mercaptoguanosine (8-MGuo) to induce polyclonal proliferation and differentiation of B cells from a variety of mouse strains. In the present study, we have defined the cellular target of this mitogenic activity. Using B cells fractionated according to size, we have found that large B cells are responsive to 8-BrGuo- and 8-MGuo-induced proliferation and differentiation whereas small, resting B cells are relatively unresponsive to these compounds. Addition of splenic adherent cells to the small B-cell fraction partially restored the proliferative but not the differentiative responses to 8-BrGuo and 8-MGuo. Although small B cells alone did not proliferate or differentiate in response to 8-BrGuo and 8-MGuo, cell surface expression of Ia antigens increased following incubation with these compounds. Thus, the biological activity of 8-BrGuo and 8-MGuo appears to be dictated by the cell type upon which it is acting. Small B cells are activated as evidenced by increased levels of surface Ia whereas large B cells are not only activated but are also induced to proliferate and differentiate.

摘要

先前的研究已证明8-溴鸟苷(8-BrGuo)和8-巯基鸟苷(8-MGuo)能够诱导多种小鼠品系的B细胞发生多克隆增殖和分化。在本研究中,我们确定了这种促有丝分裂活性的细胞靶点。通过使用按大小分离的B细胞,我们发现大型B细胞对8-BrGuo和8-MGuo诱导的增殖和分化有反应,而小型、静止的B细胞对这些化合物相对无反应。将脾黏附细胞添加到小型B细胞组分中,部分恢复了对8-BrGuo和8-MGuo的增殖反应,但未恢复分化反应。尽管单独的小型B细胞对8-BrGuo和8-MGuo没有增殖或分化反应,但与这些化合物孵育后,Ia抗原的细胞表面表达增加。因此,8-BrGuo和8-MGuo的生物学活性似乎取决于其作用的细胞类型。小型B细胞被激活,表现为表面Ia水平升高,而大型B细胞不仅被激活,还被诱导增殖和分化。

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