Literature DB >> 8690895

Frequency of VH81x usage during B cell development: initial decline in usage is independent of Ig heavy chain cell surface expression.

A J Marshall1, G E Wu, G J Paige.   

Abstract

B cell development is marked by changes in the pattern of VH segment utilization. B cell precursors characteristically utilize a restricted set of VH segments, while mature B cell populations use a wide range of VH segments. VH81x is an example of a VH segment that is highly utilized in B cell precursors, but rarely utilized in mature B cells. We have developed an assay that allows us to determine the proportion of VDJH rearrangements that utilize the VH81x segment in DNA from selected populations of developing B cells. Consistent with previous observations, it was found that VH81x is utilized at a remarkably high frequency in primary B cell progenitors. The extent of overutilization was found to be identical during fetal and adult B cell development. Phenotypic analyses demonstrated that the decline in VH81x utilization begins at a stage before the expression of IgM on the cell surface and continues through later stages of B cell development. Strikingly, mutant mice that cannot express Ig heavy chain on the cell surface displayed a drop in VH81x utilization during both fetal and adult B cell development. Together, these data suggest that mechanisms other than cellular selection play an important role in determining the shift in VH segment utilization during B cell development.

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Year:  1996        PMID: 8690895

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  22 in total

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Journal:  Immunology       Date:  2000-05       Impact factor: 7.397

2.  IkappaBalpha/IkappaBepsilon deficiency reveals that a critical NF-kappaB dosage is required for lymphocyte survival.

Authors:  Bertrand Goudeau; François Huetz; Sandrine Samson; James P Di Santo; Ana Cumano; Amer Beg; Alain Israël; Sylvie Mémet
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-09       Impact factor: 11.205

3.  Changes in histone acetylation are associated with differences in accessibility of V(H) gene segments to V-DJ recombination during B-cell ontogeny and development.

Authors:  Kristen Johnson; Cristina Angelin-Duclos; Sinae Park; Kathryn L Calame
Journal:  Mol Cell Biol       Date:  2003-04       Impact factor: 4.272

4.  Dual role of RAG2 in V(D)J recombination: catalysis and regulation of ordered Ig gene assembly.

Authors:  S A Kirch; G A Rathbun; M A Oettinger
Journal:  EMBO J       Date:  1998-08-17       Impact factor: 11.598

5.  Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities.

Authors:  S R McKercher; B E Torbett; K L Anderson; G W Henkel; D J Vestal; H Baribault; M Klemsz; A J Feeney; G E Wu; C J Paige; R A Maki
Journal:  EMBO J       Date:  1996-10-15       Impact factor: 11.598

6.  Notch signaling is necessary for adult, but not fetal, development of RORγt(+) innate lymphoid cells.

Authors:  Cécilie Possot; Sandrine Schmutz; Sylvestre Chea; Laurent Boucontet; Anne Louise; Ana Cumano; Rachel Golub
Journal:  Nat Immunol       Date:  2011-09-11       Impact factor: 25.606

7.  The CDR-H3 repertoire from TdT-deficient adult bone marrow is a close, but not exact, homologue of the CDR-H3 repertoire from perinatal liver.

Authors:  Robert L Schelonka; Ivaylo I Ivanov; Andre M Vale; Ewa Szymanska; Michael Zemlin; G Larry Gartland; Harry W Schroeder
Journal:  J Immunol       Date:  2010-10-18       Impact factor: 5.422

8.  Stepwise activation of the immunoglobulin mu heavy chain gene locus.

Authors:  D Chowdhury; R Sen
Journal:  EMBO J       Date:  2001-11-15       Impact factor: 11.598

Review 9.  Role of the BCR complex in B cell development, activation, and leukemic transformation.

Authors:  Susan R Rheingold; Valerie I Brown; Junjie Fang; Jenny M Kim; Stephan A Grupp
Journal:  Immunol Res       Date:  2003       Impact factor: 2.829

10.  Two distinct populations of H chain-edited B cells show differential surrogate L chain dependence.

Authors:  Pamela B Nakajima; Kerstin Kiefer; Amy Price; Gayle C Bosma; Melvin J Bosma
Journal:  J Immunol       Date:  2009-03-15       Impact factor: 5.422

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