Characterization of the CDR3 region of rearranged α heavy chain genes in human fetal liver

Author:

Baskin B1,Islam K B2,Smith C I E12

Affiliation:

1. Department of Biosciences, NOVUM, Karolinska Institute and Department of Immunology, Microbiology, Pathology and Infectious Diseases

2. Clinical Research Centre, Unit for Gene Therapy Research, Huddinge University Hospital, Huddinge, Sweden

Abstract

SUMMARY The human fetal liver is an early site for B cell development. Pre B cells are first detectable in human fetal life at 8 weeks of gestation, when the rearrangement of the μ heavy chain genes starts. In this study we characterize the CDR3 region of rearranged α heavy chain transcripts from four human fetal livers ranging from 8 to 11 weeks of gestation. Each fetal liver showed a limited number of variations in CDR3 sequences compared with adult peripheral blood mononuclear cells (PBMC). Sequence analysis of 91 clones demonstrated that there was no preference for the usage of a certain JH gene segment, whereas a preference for usage of DH family genes, DXP and DLR, was seen in most cases during early fetal life. This is the first study where rearranged α heavy chain genes in fetal liver have been characterized. Our data suggest that the usage of JH genes is random, while there is a preference for DH family genes in human fetal liver.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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