V(D)J recombinatorial repertoire diversification during intraclonal pro-B to B-cell differentiation

Author:

Wang Yui-Hsi1,Zhang Zhixin1,Burrows Peter D.1,Kubagawa Hiromi1,Bridges S. Louis1,Findley Harry W.1,Cooper Max D.1

Affiliation:

1. From the Division of Developmental and Clinical Immunology, and Departments of Medicine, Pediatrics, Pathology, and Microbiology, University of Alabama at Birmingham and the Howard Hughes Medical Institute, Birmingham, AL; and Division of Pediatric Hematology/Oncology/Bone Marrow Transplantation, Emory University School of Medicine, Atlanta, GA.

Abstract

Abstract The initial B-cell repertoire is generated by combinatorial immunoglobulin V(D)J gene segment rearrangements that occur in a preferential sequence. Because cellular proliferation occurs during the course of these rearrangement events, it has been proposed that intraclonal diversification occurs during this phase of B-cell development. An opportunity to examine this hypothesis directly was provided by the identification of a human acute lymphoblastic leukemic cell line that undergoes spontaneous differentiation from pro-B cell to the pre-B and B-cell stages with concomitant changes in the gene expression profile that normally occur during B-cell differentiation. After confirming the clonality of the progressively differentiating cells, an analysis of immunoglobulin genes and transcripts indicated that pro-B cell members marked by the same DJ rearrangement generated daughter B cells with multiple VH and VL gene segment rearrangements. These findings validate the principle of intraclonal V(D)J diversification during B-cell generation and define a manipulable model of human B-cell differentiation.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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