Jeong Y, Osborne B A, Goldsby R A
Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst 01002, USA.
Immunology. 2001 May;103(1):26-34. doi: 10.1046/j.1365-2567.2001.01227.x.
This study examined a number of tissues during early gestation in foetal sheep to determine the earliest site of Vlambda expression and time of generation of the Vlambda repertoire. Tissues, including spleen, liver, gut, blood and bone marrow, were obtained from 48, 55, 60 and 63 gestational day (g.d.) ovine foetuses and cDNA libraries were prepared from them by reverse transcription-polymerase chain reaction. Clones were randomly selected from cDNA libraries and subjected to sequencing. Analysis of these sequences and comparison with a pool of germline genes led to the following conclusions. The expression of Vlambda occurs earlier in spleen (48 g.d.) than in all of the other tissues examined. Also, diversity is seen earlier and at higher levels in early foetal spleen than in all of the other tissues examined. In this regard, it is notable that splenic Vlambda expression is readily apparent even before such gut-associated lymphoid tissue as the ileal Peyer's patch (IPP) has developed. Two germline Vlambda genes, 5.1 and 5.3 predominate in early immunoglobulin lambda light-chain gene rearrangement. Examination of Jlambda usage revealed the existence of a new Jlambda gene and its utilization during the early phases of the development of the ovine antibody repertoire. This study indicates that sites other than the IPP contribute to the diversification of the Vlambda repertoire in sheep. We suggest that it is likely that foetal spleen may provide a partially diversified B-cell repertoire before the IPP becomes active as a major site for massive clonal expansion and extensive diversification of B cells.
本研究检测了胎羊妊娠早期的多个组织,以确定Vλ表达的最早部位和Vλ库产生的时间。从妊娠48、55、60和63天的绵羊胎儿获取包括脾脏、肝脏、肠道、血液和骨髓在内的组织,并通过逆转录-聚合酶链反应从这些组织中制备cDNA文库。从cDNA文库中随机选择克隆并进行测序。对这些序列进行分析并与种系基因库进行比较,得出以下结论。Vλ在脾脏(妊娠48天)中的表达比在所有其他检测组织中更早出现。此外,与所有其他检测组织相比,胎儿早期脾脏中多样性出现得更早且水平更高。在这方面,值得注意的是,即使在诸如回肠派伊尔结(IPP)这样的肠道相关淋巴组织发育之前,脾脏Vλ表达就已经很明显了。两个种系Vλ基因5.1和5.3在早期免疫球蛋白λ轻链基因重排中占主导地位。对Jλ使用情况的检测揭示了一个新的Jλ基因的存在及其在绵羊抗体库发育早期阶段的利用。本研究表明,IPP以外的部位对绵羊Vλ库的多样化有贡献。我们认为,在IPP作为B细胞大规模克隆扩增和广泛多样化的主要部位变得活跃之前,胎儿脾脏可能提供了部分多样化的B细胞库。