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单体免疫球蛋白对B细胞分化的反馈抑制

Feedback inhibition of B cell differentiation by monomeric immunoglobulin.

作者信息

Mayer L, Stohl W, Cunningham-Rundles C

机构信息

Mount Sinai Medical Center, New York, New York, USA.

出版信息

Int Rev Immunol. 1989;5(2):189-95. doi: 10.3109/08830188909061986.

Abstract

Polyspecific monomeric immunoglobulin (Ig) isolated from either a commercial source (pooled, > 2000 donors), or an autologous donor was capable of inhibiting both B cell proliferation, induced by T dependent mitogens or T cell factors and B cell differentiation, induced by similar stimuli. These effects appear to be directed at the B cell itself since inhibition of differentiation is detectable when monomeric Ig is added to cultures of B cell lines in the presence of B cell differentiation factor (BCDF). The inhibition of B cell differentiation does not appear to relate to inhibition of B cell proliferation, as no detectable change is seen in thymidine incorporation or cell number in these cultures. Furthermore, the effect of monomeric lg appears to relate to an early event in B cell differentiation, as there is no effect of IgSRK on spontaneously secreting B cell lines and maturation to cytoplasmic Ig containing cells is markedly impaired. Therefore, monomeric Ig secreted by B cells may serve as an immunoregulator of further Ig secretion.

摘要

从商业来源(汇集自>2000名供体)或自体供体中分离出的多特异性单体免疫球蛋白(Ig)能够抑制由T细胞依赖性丝裂原或T细胞因子诱导的B细胞增殖以及由类似刺激诱导的B细胞分化。这些效应似乎是直接作用于B细胞本身,因为当在存在B细胞分化因子(BCDF)的情况下将单体Ig添加到B细胞系培养物中时,可检测到分化受到抑制。B细胞分化的抑制似乎与B细胞增殖的抑制无关,因为在这些培养物中胸苷掺入或细胞数量没有可检测到的变化。此外,单体Ig的作用似乎与B细胞分化的早期事件有关,因为IgSRK对自发分泌的B细胞系没有影响,并且向含有细胞质Ig的细胞的成熟明显受损。因此,B细胞分泌的单体Ig可能作为进一步Ig分泌的免疫调节剂。

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