Ohama Y, Adler L T
Cell Immunol. 1984 Jul;86(2):429-38. doi: 10.1016/0008-8749(84)90398-8.
Regulation of immunoglobulin synthesis and secretion was analyzed by exposing spleen cells of b4b4 rabbits to anti-b4 for 24 hr in culture. As noted previously, no lymphocytes with membrane-bound b4 were found immediately after pulse treatment, but substantial regeneration of membrane Ig (mIg) occurred on further culture in antibody-free medium. Splenocytes cultured either in the presence or absence of anti-b4 showed a marked loss of Ig-secreting cells (ISC) after 24 hr in culture but recovered and exhibited peak numbers of ISC on Day 2. However, ISC formation in cultures of antibody-treated cells was significantly suppressed and thereafter declined at a more rapid rate than in control cultures. Polyclonal B cell activators from Nocardia and from gram-negative bacteria stimulated ISC formation in cultures of normal spleen cells, but responsiveness to these activators was depressed following antibody treatment. Antibody-induced suppression of Ig synthesis was attributed to interference with differentiation of B lymphocytes to the secretory stage.
通过在培养中将b4b4兔的脾细胞暴露于抗b4 24小时,分析免疫球蛋白合成和分泌的调节。如先前所述,脉冲处理后立即未发现带有膜结合b4的淋巴细胞,但在无抗体培养基中进一步培养时,膜免疫球蛋白(mIg)大量再生。在有或没有抗b4的情况下培养的脾细胞在培养24小时后显示出分泌免疫球蛋白细胞(ISC)的明显损失,但恢复并在第2天表现出ISC的峰值数量。然而,抗体处理细胞培养物中的ISC形成受到显著抑制,此后以比对照培养物更快的速度下降。来自诺卡氏菌和革兰氏阴性菌的多克隆B细胞激活剂刺激正常脾细胞培养物中的ISC形成,但抗体处理后对这些激活剂的反应性降低。抗体诱导的免疫球蛋白合成抑制归因于对B淋巴细胞向分泌阶段分化的干扰。