Genotypic analysis of B cell colonies by in situ hybridization. Stoichiometric expression of three VH families in adult C57BL/6 and BALB/c mice.
Abstract
The filter paper disc method for cloning inducible lymphocytes was used to census
the splenic B cell population of C57BL/6 and BALB/c mice for the expression of three
VH gene-families, VH X-24, -Q52, and -J558. B cell colonies, arising from single founder
lymphocytes, were identified by in situ hybridization with VH family- and C mu-specific
cDNA probes. Some 6.7 X 10(4) C mu+ colonies were screened. Among C57BL/6- or BALB/c-derived
colonies, approximately 3% were VH X-24+, approximately 19% were VH Q52+, and approximately
54% were VH J558+. These frequencies are consistent with a process of equiprobable
expression for individual VH segments, and provide direct evidence that normal splenic
B lymphocytes use a process of random genetic combinatorics to generate the antibody
repertoire.
Type
Journal articleSubject
AnimalsAntibody Diversity
B-Lymphocytes
Cell Division
Cell Line
DNA
Genetic Variation
Genotype
Immunoglobulin Heavy Chains
Immunoglobulin Variable Region
Lipopolysaccharides
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Nucleic Acid Hybridization
Spleen
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https://hdl.handle.net/10161/10896Collections
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Show full item recordScholars@Duke
Garnett H. Kelsoe
James B. Duke Distinguished Professor of Immunology
1. Lymphocyte development and antigen-driven diversification of immunoglobulin and
T cell antigen receptor genes. 2. The germinal center reaction and mechanisms for
clonal selection and self - tolerance. The origins of autoimmunity. 3. Interaction
of innate- and adaptive immunity and the role of inflammation in lymphoid organogenesis.
4. The role of secondary V(D)J gene rearrangment in lymphocyte development and malignancies.
5. Mathematical modeling of immune responses,

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