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通过显微注射来自脂多糖刺激的正常淋巴细胞的细胞质因子来恢复C3H/HeJ小鼠淋巴细胞对脂多糖的反应性。

Restoration of LPS responsiveness of C3H/HeJ mouse lymphocytes by microinjection of cytoplasmic factor(s) from LPS-stimulated normal lymphocytes.

作者信息

Eda Y, Ohara J, Watanabe T

出版信息

J Immunol. 1983 Sep;131(3):1294-9.

PMID:6604094
Abstract

Cytosol fractions of lymphocytes from LPS-responder mice (C3H/HeN) were prepared and injected into B lymphocytes of LPS-nonresponder mice (C3H/HeJ) by a microinjection technique utilizing polyethyleneglycol-mediated cell fusion. The B lymphocytes of C3H/HeJ mice microinjected with cytosol prepared from LPS-stimulated C3H/HeN cells became normally responsive to LPS. Microinjection of cytosol itself did not stimulate C3H/HeJ cells to proliferate or differentiate into immunoglobulin-producing cells, and the cells injected with cytosol had to be restimulated with LPS in order to proliferate and differentiate. These data suggested that C3H/HeJ B cells acquired LPS responsiveness by microinjection of cytoplasmic factor(s) from LPS-stimulated C3H/HeN cells and that these factor(s) may be one of the components involved in normal signal transmission from cell surface to nucleus in the early stages of the LPS response. The apparent m.w. of the cytoplasmic factor(s) is 100,000 by gel filtration. Chromatofocusing analysis suggested that these factors may consist of two components with the same m.w.

摘要

利用聚乙二醇介导的细胞融合显微注射技术,制备了脂多糖应答小鼠(C3H/HeN)淋巴细胞的胞质溶胶组分,并将其注射到脂多糖无应答小鼠(C3H/HeJ)的B淋巴细胞中。用从脂多糖刺激的C3H/HeN细胞制备的胞质溶胶显微注射的C3H/HeJ小鼠的B淋巴细胞对脂多糖恢复正常应答。显微注射胞质溶胶本身并不会刺激C3H/HeJ细胞增殖或分化为产生免疫球蛋白的细胞,注射了胞质溶胶的细胞必须用脂多糖再次刺激才能增殖和分化。这些数据表明,C3H/HeJ B细胞通过显微注射来自脂多糖刺激的C3H/HeN细胞的细胞质因子而获得了对脂多糖的应答能力,并且这些因子可能是脂多糖应答早期从细胞表面到细胞核的正常信号传递所涉及的成分之一。通过凝胶过滤法测得细胞质因子的表观分子量为100,000。层析聚焦分析表明,这些因子可能由两个分子量相同的成分组成。

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