Cutting Edge: Impaired Transitional B Cell Production and Selection in the Nonobese Diabetic Mouse
Author(s) -
William J. Quinn,
Negin Noorchashm,
Jenni E. Crowley,
Amy J. Reed,
Hooman Noorchashm,
Ali Naji,
Michael P. Cancro
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.176.12.7159
Subject(s) - nod , biology , b cell , selection (genetic algorithm) , negative selection , bone marrow , microbiology and biotechnology , cell , mouse strain , follicular phase , immunology , endocrinology , antibody , genetics , diabetes mellitus , gene , genome , artificial intelligence , computer science
Developing B cells undergo selection at multiple checkpoints to eliminate autoreactive clones. We analyzed B cell kinetics in the NOD mouse to establish whether these checkpoints are intact. Our results show that although bone marrow production is normal in NOD mice, transitional (TR) B cell production collapses at 3 wk of age, reflecting a lack of successful immature B cell migration to the periphery. This yields delayed establishment of the follicular pool and a lack of selection at the TR checkpoint, such that virtually all immature B cells that exit the bone marrow mature without further selection. These findings suggest that compromised TR B cell generation in NOD mice yields relaxed TR selection, affording autoreactive specificities access to mature pools.
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