Holmberg D, Lundkvist I, Forni L, Ivars F, Coutinho A
Department of Immunology, Umeå University, Basel Institute for Immunology, Paris, France.
J Mol Cell Immunol. 1985;2(1):51-6.
A few hundred hybridoma cell lines derived from spleen cells of normal, nonimmunized, 6-day-old BALB/c or BALB.B10 mice were screened for H- and L-chain production. Roughly half of these hybridomas produced no Ig chain into the culture supernatants. Of the Ig-secretors, 80% produced IgM molecules carrying either kappa or lambda chains in a ratio of 9:1. A surprisingly high frequency of clones (roughly 20%) were found to produce only light chains and in this group, the kappa/lambda ratio was altered to around 1. The indications from the primary screening were confirmed by isolating a large number of these hybrid cell lines and extensive testing of both culture supernatants and ascitic fluids in solid phase RIA and ELISA assays. In some cases, the absence or presence of heavy chain synthesis and the isotype of the light chain was also confirmed by biosynthetic labeling of the hybridoma clones, specific immuno-precipitation of cell lysates or supernatants, followed by analysis in SDS polyacrylamide gels. We conclude from these results that the absence of heavy chain expression is accompanied by frequencies of lambda chain expression, which are much higher than those observed in normal immunoglobulin producing cells, and equal to those of kappa chains. This conclusion can be interpreted as to suggest that the low frequency of lambda producing cells in mouse is in part determined by restrictions in the heavy-light chain interactions at the protein level.(ABSTRACT TRUNCATED AT 250 WORDS)
从正常、未免疫的6日龄BALB/c或BALB.B10小鼠的脾细胞中获得了数百个杂交瘤细胞系,并对其H链和L链的产生进行了筛选。这些杂交瘤中约有一半没有向培养上清液中分泌Ig链。在分泌Ig的细胞中,80%产生携带κ链或λ链的IgM分子,其比例为9:1。令人惊讶的是,发现有相当高比例的克隆(约20%)只产生轻链,在这一组中,κ/λ比例改变为约1。通过分离大量这些杂交细胞系,并在固相RIA和ELISA分析中对培养上清液和腹水进行广泛检测,证实了初步筛选的结果。在某些情况下,还通过对杂交瘤克隆进行生物合成标记、对细胞裂解物或上清液进行特异性免疫沉淀,然后在SDS聚丙烯酰胺凝胶中进行分析,来确认重链合成的缺失或存在以及轻链的同种型。从这些结果我们得出结论,重链表达的缺失伴随着λ链表达的频率,该频率远高于在正常产生免疫球蛋白的细胞中观察到的频率,且与κ链的频率相当。这一结论可以解释为,小鼠中产生λ链细胞的低频率部分是由蛋白质水平上重链与轻链相互作用的限制所决定的。(摘要截短于250字)