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来自CBA/N小鼠的脾B细胞在用链霉蛋白酶短暂处理后获得对抗免疫球蛋白的反应性。

Splenic B cells from CBA/N mice acquire responsiveness to anti-immunoglobulin after a brief treatment with pronase.

作者信息

Ramanadham M, Gollapudi S V, Kern M

出版信息

J Immunol. 1985 Jan;134(1):4-6.

PMID:3871111
Abstract

Although splenic B cells of CBA/N mice do not synthesize DNA in response to anti-mouse IgM (mu-chain specific), the cells respond readily to Sepharose linked anti-mu. Subsequent to a brief treatment with pronase, CBA/N splenocytes exhibited anti-mu-mediated DNA synthesis at 40 to 100% of the DNA synthetic capacity detected with Sepharose linked anti-mu. Furthermore, spleen cell populations treated with anti-Thy-1.2 and complement or populations purified on anti-immunoglobulin-coated Petri plates (greater than 90% surface immunoglobulin positive) acquired responsiveness to anti-mu after pronase treatment.

摘要

尽管CBA/N小鼠的脾脏B细胞不会因抗小鼠IgM(μ链特异性)而合成DNA,但这些细胞对交联抗μ的琼脂糖凝胶反应迅速。在用链霉蛋白酶进行短暂处理后,CBA/N脾细胞表现出抗μ介导的DNA合成,其合成能力为交联抗μ琼脂糖凝胶检测到的DNA合成能力的40%至100%。此外,用抗Thy-1.2和补体处理的脾细胞群体,或在抗免疫球蛋白包被的培养皿上纯化的群体(表面免疫球蛋白阳性率大于90%),在经链霉蛋白酶处理后获得了对抗μ的反应性。

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