Abstract

Studies in humans and mice indicate the critical role of the surrogate light chain in the selection of the productive immunoglobulin repertoire during B cell development. However, subsequent studies using mutant mice have also demonstrated that alternative pathways are allowed. Our recent investigation has shown that some species, such as pig, physiologically use preferential rearrangement of authentic light chains, and become independent of surrogate light chains. Here we summarize the findings from swine and compare them with results in other species. In both groups, allelic and isotypic exclusions remain intact, so the different processes do not alter the paradigm of B-cell monospecificity. Both groups also retained some other essential processes, such as segregated and sequential rearrangement of heavy and light chain loci, preferential rearrangement of light chain kappa before lambda, and functional κ-deleting element recombination. On the other hand, the respective order of heavy and light chains rearrangement may vary, and rearrangement of the light chain kappa and lambda on different chromosomes may occur independently. Studies have also confirmed that the surrogate light chain is not required for the selection of the productive repertoire of heavy chains and can be substituted by authentic light chains. These findings are important for understanding evolutional approaches, redundancy and efficiency of B-cell generation, dependencies on other regulatory factors, and strategies for constructing therapeutic antibodies in unrelated species. The results may also be important for explaining interspecies differences in the proportional use of light chains and for the understanding of divergences in rearrangement processes. Therefore, the division into two groups may not be definitive and there may be more groups of intermediate species.

Highlights

  • Immunoglobulin (Ig) gene rearrangement has evolved in all jawed vertebrates and involves recombination of variable (V), diversity (D), and joining (J) gene segments at their corresponding loci

  • Different species appear to have evolved different strategies for the order of rearrangement of Ig genes and for the selection of a productive Ig repertoire. Possibilities for these strategies have even been indicated in mice themselves, which showed that the order of rearrangement is independent (27, 40, 41) and surrogate light chain (SLC) is unnecessary (47, 48)

  • All these species have survived with comparable success

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Summary

Introduction

Immunoglobulin (Ig) gene rearrangement has evolved in all jawed vertebrates and involves recombination of variable (V), diversity (D), and joining (J) gene segments at their corresponding loci (reviewed in 1). Initial IgL rearrangements in the absence of IgH can be expressed on the cell surface of early precursors in swine (8, 10). Studies in pigs extended these findings from the perspective of species which use IgL before IgH rearrangement and confirmed that multiple and even productive IgLl rearrangements are present in IgLk+ B cells (8, 10–12).

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