Chen J, Herzenberg L A, Herzenberg L A
Department of Genetics, Stanford University, CA 94305.
Int Immunol. 1991 Nov;3(11):1117-27. doi: 10.1093/intimm/3.11.1117.
Studies presented here show that heparin alters immunoglobulin expression by murine pre-B cell lines and normal Ly-1 (CD5+) B cells. Previous studies have shown that pre-B cell lines 70Z/3 and NFS-5.3 express mu heavy chains in the cytoplasm and a small amount on the cell surface. Both these cytoplasmic and surface mu are disulfide-linked to omega (lambda 5) surrogate light chains and are noncovalently associated with iota (Vpre-B) variable region-like proteins. We show that culturing 70Z/3 with heparin reduces the amount of the membrane-form mu (micron) on the cell surface. Culturing NFS-5.3 with heparin similarly decreases the membrane-form mu; however, it increases the surface level of a pentameric mu molecule containing secreted-form mu (microS) heavy chains, disulfide-linked omega (lambda 5) chains, and noncovalently associated proteins. Culturing peritoneal B cells with heparin also increases the production of the secreted-form microS, detectable in this case by the secretion of classical pentameric IgM. Similarly, injecting heparin intraperitoneally increases IgM secretion by peritoneal Ly-1 B cells. Thus heparin could influence pre-B cell and B cell differentiation and function.
此处展示的研究表明,肝素可改变小鼠前B细胞系和正常Ly-1(CD5+)B细胞的免疫球蛋白表达。先前的研究表明,前B细胞系70Z/3和NFS-5.3在细胞质中表达μ重链,在细胞表面表达少量μ重链。这些细胞质和表面的μ重链均通过二硫键与ω(λ5)替代轻链相连,并与ι(Vpre-B)可变区样蛋白非共价结合。我们发现,用肝素培养70Z/3可减少细胞表面膜形式μ(μm)的量。用肝素培养NFS-5.3同样会减少膜形式μ;然而,它会增加含有分泌形式μ(μS)重链、二硫键连接的ω(λ5)链和非共价结合蛋白的五聚体μ分子的表面水平。用肝素培养腹膜B细胞也会增加分泌形式μS的产生,在这种情况下可通过经典五聚体IgM的分泌检测到。同样,腹膜内注射肝素可增加腹膜Ly-1 B细胞的IgM分泌。因此,肝素可能影响前B细胞和B细胞的分化及功能。