Kinashi T, Inaba K, Tsubata T, Tashiro K, Palacios R, Honjo T
Department of Medical Chemistry, Kyoto University, Japan.
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4473-7. doi: 10.1073/pnas.85.12.4473.
Precursors to B-cell lines with immunoglobulin genes in the germ-line context have been shown to be capable of generating mature B cells in vivo. We report here that an interleukin 3-dependent precursor B-cell line, LyD9, differentiated in vitro into mature B cells, producing IgM and IgG by coculture with bone marrow accessory (or stroma) cells or with dendritic cells and T cells. Up to 50% of IgM-positive cells, but no Thy-1-positive cells, appeared after the 7- to 10-day coculture. Induced LyD9 cells underwent heterogenous immunoglobulin gene rearrangement and synthesized mRNAs encoding immunoglobulin mu, gamma, and kappa chains. However, these cells did not show any rearrangement of genes encoding the alpha and beta chains of the T-cell receptor. The induction of differentiation by coculture with bone marrow stroma cells was blocked by anti-lymphocyte function-associated antigen 1 or anti-interleukin 4 antibody. These systems are useful for molecular biological studies on regulation of differentiation of bone marrow-derived cells into the B-cell lineage.
在种系背景下带有免疫球蛋白基因的B细胞系前体已被证明能够在体内产生成熟的B细胞。我们在此报告,一种依赖白细胞介素3的前体B细胞系LyD9,通过与骨髓辅助(或基质)细胞、或与树突状细胞及T细胞共培养,在体外分化为成熟的B细胞,产生IgM和IgG。7至10天的共培养后,出现了高达50%的IgM阳性细胞,但未出现Thy-1阳性细胞。诱导的LyD9细胞经历了异源免疫球蛋白基因重排,并合成了编码免疫球蛋白μ、γ和κ链的mRNA。然而,这些细胞未显示出编码T细胞受体α和β链的基因发生任何重排。与骨髓基质细胞共培养诱导的分化被抗淋巴细胞功能相关抗原1或抗白细胞介素4抗体阻断。这些体系对于骨髓来源细胞向B细胞系分化调控的分子生物学研究很有用。