Kearney J F, Cooper M D, Lawton A R
J Immunol. 1976 Jun;116(6):1664-8.
Lipopolysaccharide-(LPS) induced differentiation of mouse B lymphocytes to cells synthesizing large amounts of cytoplasmic IgM and IgG2 could be suppressed by antibodies to mu-chains. Maximal inhibition of LPS-induced differentiation was associated with increased cellular proliferation as measured by incorporation of 3H-thymidine, whereas treatment with anti-mu alone over a wide dosage range did not stimulate cellular proliferation. Spleen cells from newborn mice were suppressed by concentrations of anti-mu several hundred-fold lower than required for adult spleen cells; the adult pattern of susceptibility to suppression was acquired by 1 week of age. No significant differences in susceptibility to anti-mu were found in comparisons of adult spleen, lymph node, bone marrow, and Peyer's patch lymphocytes.
脂多糖(LPS)诱导的小鼠B淋巴细胞向合成大量细胞质IgM和IgG2的细胞分化可被抗μ链抗体抑制。通过3H-胸腺嘧啶核苷掺入量测定,LPS诱导分化的最大抑制与细胞增殖增加有关,而在宽剂量范围内单独使用抗μ治疗不会刺激细胞增殖。新生小鼠的脾细胞被抗μ浓度抑制,该浓度比成年脾细胞所需浓度低数百倍;成年小鼠对抑制的易感性模式在1周龄时获得。在成年脾、淋巴结、骨髓和派尔集合淋巴结淋巴细胞的比较中,未发现对抗μ易感性的显著差异。