Department of Microbiology and Immunology, University of Maryland, Baltimore, MD 21201.
Department of Microbiology and Immunology, University of Maryland, Baltimore, MD 21201
J Immunol. 2014 Oct 1;193(7):3248-55. doi: 10.4049/jimmunol.1400531.
Joining chain (J chain) is a small polypeptide that regulates multimerization of secretory IgM and IgA, the only two mammalian Igs capable of forming multimers. J chain also is required for poly-Ig receptor-mediated transport of these Ig classes across the mucosal epithelium. It is generally assumed that all plasma cells express J chain regardless of expressed isotype, despite the documented presence of J chain(-) plasma cells in mammals, specifically in all monomeric IgA-secreting cells and some IgG-secreting cells. Compared with most other immune molecules, J chain has not been studied extensively, in part because of technical limitations. Even the reported phenotype of the J chain-knockout mouse is often misunderstood or underappreciated. In this short review, we discuss J chain in light of the various proposed models of its expression and regulation, with an added focus on its evolutionary significance, as well as its expression in different B cell lineages/differentiation states.
连接链 (J 链) 是一种小的多肽,可调节分泌型 IgM 和 IgA 的多聚化,这是仅有的两种能够形成多聚体的哺乳动物 Ig。J 链还需要多 Ig 受体介导这些 Ig 类别的跨黏膜上皮运输。通常认为所有浆细胞都表达 J 链,而不管表达的同种型如何,尽管有文献报道哺乳动物中存在 J 链(-)浆细胞,特别是在所有单体 IgA 分泌细胞和一些 IgG 分泌细胞中。与大多数其他免疫分子相比,J 链的研究还不够广泛,部分原因是技术限制。即使是报道的 J 链敲除小鼠的表型也经常被误解或低估。在这篇简短的综述中,我们根据 J 链表达和调节的各种提出的模型来讨论 J 链,额外关注其进化意义,以及其在不同 B 细胞谱系/分化状态中的表达。