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Fc Receptor-Like 6 (FCRL6) Discloses Progenitor B Cell Heterogeneity That Correlates With Pre-BCR Dependent and Independent Pathways of Natural Antibody Selection

B-1a cells produce “natural” antibodies (Abs) to neutralize pathogens and clear neo self-antigens, but the fundamental selection mechanisms that shape their polyreactive repertoires are poorly understood. Here, we identified a B cell progenitor subset defined by Fc receptor-like 6 (FCRL6) expression...

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Detalles Bibliográficos
Autores principales: Honjo, Kazuhito, Won, Woong-Jai, King, Rodney G., Ianov, Lara, Crossman, David K., Easlick, Juliet L., Shakhmatov, Mikhail A., Khass, Mohamed, Vale, Andre M., Stephan, Robert P., Li, Ran, Davis, Randall S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033751/
https://www.ncbi.nlm.nih.gov/pubmed/32117244
http://dx.doi.org/10.3389/fimmu.2020.00082
Descripción
Sumario:B-1a cells produce “natural” antibodies (Abs) to neutralize pathogens and clear neo self-antigens, but the fundamental selection mechanisms that shape their polyreactive repertoires are poorly understood. Here, we identified a B cell progenitor subset defined by Fc receptor-like 6 (FCRL6) expression, harboring innate-like defense, migration, and differentiation properties conducive for natural Ab generation. Compared to FCRL6(−) pro B cells, the repressed mitotic, DNA damage repair, and signaling activity of FCRL6(+) progenitors, yielded V(H) repertoires with biased distal Ighv segment accessibility, constrained diversity, and hydrophobic and charged CDR-H3 sequences. Beyond nascent autoreactivity, V(H)11 productivity, which predominates phosphatidylcholine-specific B-1a B cell receptors (BCRs), was higher for FCRL6(+) cells as was pre-BCR formation, which was required for Myc induction and V(H)11, but not V(H)12, B-1a development. Thus, FCRL6 revealed unexpected heterogeneity in the developmental origins, regulation, and selection of natural Abs at the pre-BCR checkpoint with implications for autoimmunity and lymphoproliferative disorders.