Praz F, Ruuth E
J Exp Med. 1986 May 1;163(5):1349-54. doi: 10.1084/jem.163.5.1349.
We have investigated the effects of cleavage of factor B by its activating enzyme, factor D, as well as its activation fragments Bb and Ba, on the growth of mouse spleen B lymphocytes preactivated by LPS. Neither factor B nor factor D show any growth-supporting activity when tested alone. The coaddition of factor B and factor D to serum-free cultures of LPS-preactivated B cell blasts increased the proliferation of the responding cells up to the level obtained by restimulation with LPS. Such growth-supporting activity was shown to be mediated by Ba, whereas Bb did not show any significant effect. Furthermore, this effect was not restricted to the LPS-preactivated B cell blasts; in fact, Ba also supported the growth of in vivo, activated B cell blasts of unprimed mice of the LPS-nonresponder C3H/HeJ strain. In contrast, Ba did not maintain growth of Con A-activated T cells or TCGF-dependent CTL cells. Taken together, these results describe the first biological activity of human Ba as a B cell stimulatory factor.
我们研究了其激活酶D因子对B因子的裂解作用,以及其激活片段Bb和Ba,对经脂多糖(LPS)预激活的小鼠脾脏B淋巴细胞生长的影响。单独检测时,B因子和D因子均未显示出任何生长支持活性。将B因子和D因子共同添加到经LPS预激活的B细胞母细胞的无血清培养物中,可使反应细胞的增殖增加至用LPS再次刺激所达到的水平。这种生长支持活性被证明是由Ba介导的,而Bb未显示出任何显著作用。此外,这种作用并不局限于经LPS预激活的B细胞母细胞;事实上,Ba还支持LPS无反应性C3H/HeJ品系未致敏小鼠体内激活的B细胞母细胞的生长。相比之下,Ba不能维持伴刀豆球蛋白A(Con A)激活的T细胞或依赖白细胞介素-2(TCGF)的细胞毒性T淋巴细胞(CTL)细胞的生长。综上所述,这些结果描述了人Ba作为B细胞刺激因子的首个生物学活性。