Department of Immunology, DUMC 3010, Duke University Medical Center, Durham, NC 27710, USA.
J Immunol Methods. 2010 Mar 31;354(1-2):53-67. doi: 10.1016/j.jim.2010.01.007. Epub 2010 Jan 28.
We describe and characterize a stromal cell independent culture system that efficiently supports pro-B cell to IgM+ B cell development with near normal levels of IgH and Igkappa diversity. Pro-B cells present in non-adherent bone marrow cells proliferate in the presence of IL-7 and subsequent to the removal of IL-7 and addition of BAFF, differentiate normally into IgM+ B cells. B cell development in vitro closely follows the patterns of development in vivo with culture-derived (CD) B cells demonstrating characteristic patterns of surface antigen expression and gene activation. IgM+ CD B cells respond to TLR stimulation by proliferation and differentiation into antibody-secreting cells. Self-reactive IgM+ B cell development is blocked in 3H9 IgH knockin mice; however, cultures of 3H9 IgH knockin pro-B cells yields high frequencies of "forbidden", autoreactive IgM+ B cells. Furthermore, serum IgG autoantibody exceeded that present in autoimmune, C4(-/-) animals following the reconstitution of RAG1(-/-) mice with IgM+ CD cells derived from BL/6 mice.
我们描述并表征了一种基质细胞独立的培养系统,该系统能够高效支持前 B 细胞向 IgM+ B 细胞的发育,同时保持 IgH 和 Igkappa 多样性的正常水平。非贴壁骨髓细胞中的前 B 细胞在 IL-7 的存在下增殖,随后去除 IL-7 并添加 BAFF,正常分化为 IgM+ B 细胞。体外 B 细胞的发育与体内的发育模式非常相似,培养得到的(CD)B 细胞表现出特征性的表面抗原表达和基因激活模式。IgM+ CD B 细胞对 TLR 刺激的反应是通过增殖和分化为分泌抗体的细胞来实现的。在 3H9 IgH 敲入小鼠中,自身反应性 IgM+ B 细胞的发育被阻断;然而,3H9 IgH 敲入前 B 细胞的培养产生了高频率的“禁止”的自身反应性 IgM+ B 细胞。此外,在用来自 BL/6 小鼠的 IgM+ CD 细胞重建 RAG1(-/-) 小鼠后,血清 IgG 自身抗体的水平超过了存在于自身免疫、C4(-/-) 动物中的水平。