Home LiteratureArticle Details
PMID: 1511482 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The developmental patterns of B cell precursors distinguishing between environmental and nonenvironmental forms of phosphocholine.

Cellular immunology ·Vol. 143 ·No. 2 ·1992-09-00 ·Pages 378-88

Chen C, Bruderer U, Rittenberg MB

Abstract

We have analyzed the developmental patterns of two groups of B cell precursors in nonimmunized BALB/c mice with respect to their relative proportions, absolute frequencies, V gene usage, fine specificity, and avidity for antigen. One group of B cells (group I) secretes antibodies specific for PC and PC-containing bacteria, whereas the other group (group II) produces antibodies recognizing only nonenvironmental PC-protein conjugates. A marked shift in the proportions of group I and group II occurs during ontogeny: while the group I B cells dominate (greater than 85%) the adult antibody repertoire, the group II B cells have equal representation in neonatal mice from Days 1 to 7, and remain as a significant portion until 2 weeks of age. Examination of the absolute frequencies of group I and group II B cells revealed that the frequency of group II B cells remained relatively stable throughout ontogeny, whereas group I B cells expanded rapidly after 7 days of age to predominate in the adult. Genetic analysis indicated that early group I antibodies were encoded by VH and VL genes different from adult group I antibodies which are mostly encoded by a single VH (S107) and VL (V kappa 22) gene combination (the T15 idiotype). On the other hand, early group II antibodies used VH genes comparable to their adult counterparts. The majority of early group I antibodies have lower avidity for PC than adult T15+ antibodies, whereas the avidity of neonatal group II antibodies varies considerably and is comparable with that of the adult group II antibodies. Our results suggest that the ontogeny of phosphocholine-specific B cells may be regulated according to their fine specificity rather than to their avidity or V gene usage.

MeSH Terms
Age Factors Animals Antibody Affinity Antibody Specificity B-Lymphocytes/immunology Genes, Immunoglobulin Histones/immunology Hybridomas Immunoglobulin Heavy Chains/genetics Immunoglobulin Isotypes/immunology Immunoglobulin Variable Region/genetics Mice Mice, Inbred BALB C Phosphorylcholine/immunology Streptococcus pneumoniae/immunology
Chemicals
Histones Immunoglobulin Heavy Chains Immunoglobulin Isotypes Immunoglobulin Variable Region Phosphorylcholine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Chen C
Department of Microbiology and Immunology, Oregon Health Sciences University, Portland 97201-3098.
Bruderer U
Rittenberg M B
Article Info
Journal
Cellular immunology
Abbr.
Cell Immunol
ISSN
0008-8749
Published
1992-09-00
Pages
378-88
Language
English
Region
Netherlands
NLM ID
1246405
Subset
IM
Grants
NIAID NIH HHS · AI14985 · United States
NIAID NIH HHS · AI26827 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com