Literature DB >> 18768830

Role of beta-catenin in B cell development and function.

Qing Yu1, William J Quinn, Theresa Salay, Jenni E Crowley, Michael P Cancro, Jyoti Misra Sen.   

Abstract

beta-Catenin is a central mediator of Wnt signaling pathway, components of which have been implicated in B cell development and function. B cell progenitors and bone marrow stromal cells express Wnt ligands, Frizzled receptors and Wnt antagonists, suggesting fine tuned regulation of this pathway in B cell development. In particular, deletion of Frizzled 9 gene results in developmental defects at the pre-B stage of development and an accumulation of plasma cells. Furthermore, Wnt signals regulate B cell proliferation through lymphocyte enhancer-binding factor-1. However, it is not known whether Wnt signaling in B cell development is mediated by beta-catenin and whether beta-catenin plays a role in mature B cell function. In this report, we show that mice bearing B cell-specific deletion of beta-catenin have normal B cell development in bone marrow and periphery. A modest defect in plasma cell generation in vitro was documented, which correlated with a defective expression of IRF-4 and Blimp-1. However, B cell response to T-dependent and T-independent Ags in vivo was found to be normal. Thus, beta-catenin expression was found to be dispensable for normal B cell development and function.

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Year:  2008        PMID: 18768830      PMCID: PMC2575415          DOI: 10.4049/jimmunol.181.6.3777

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


  26 in total

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Journal:  Annu Rev Immunol       Date:  2001       Impact factor: 28.527

2.  Deletion of beta-catenin impairs T cell development.

Authors:  Youyuan Xu; Daliya Banerjee; Joerg Huelsken; Walter Birchmeier; Jyoti Misra Sen
Journal:  Nat Immunol       Date:  2003-11-09       Impact factor: 25.606

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Authors:  Juli P Miller; David Allman
Journal:  J Immunol       Date:  2003-09-01       Impact factor: 5.422

4.  Resolution of three nonproliferative immature splenic B cell subsets reveals multiple selection points during peripheral B cell maturation.

Authors:  D Allman; R C Lindsley; W DeMuth; K Rudd; S A Shinton; R R Hardy
Journal:  J Immunol       Date:  2001-12-15       Impact factor: 5.422

5.  Blimp-1 is required for the formation of immunoglobulin secreting plasma cells and pre-plasma memory B cells.

Authors:  Miriam Shapiro-Shelef; Kuo-I Lin; Louise J McHeyzer-Williams; Jerry Liao; Michael G McHeyzer-Williams; Kathryn Calame
Journal:  Immunity       Date:  2003-10       Impact factor: 31.745

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Authors:  Sherri L Christian; Peter V Sims; Michael R Gold
Journal:  J Immunol       Date:  2002-07-15       Impact factor: 5.422

7.  Simultaneous loss of beta- and gamma-catenin does not perturb hematopoiesis or lymphopoiesis.

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8.  Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development.

Authors:  V Brault; R Moore; S Kutsch; M Ishibashi; D H Rowitch; A P McMahon; L Sommer; O Boussadia; R Kemler
Journal:  Development       Date:  2001-04       Impact factor: 6.868

9.  Nuclear factor kappa B is required for the development of marginal zone B lymphocytes.

Authors:  A Cariappa; H C Liou; B H Horwitz; S Pillai
Journal:  J Exp Med       Date:  2000-10-16       Impact factor: 14.307

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Authors:  Monica Cobas; Anne Wilson; Bettina Ernst; Stéphane J C Mancini; H Robson MacDonald; Rolf Kemler; Freddy Radtke
Journal:  J Exp Med       Date:  2004-01-12       Impact factor: 14.307

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Review 5.  Wnt-related molecules and signaling pathway equilibrium in hematopoiesis.

Authors:  Sachin Malhotra; Paul W Kincade
Journal:  Cell Stem Cell       Date:  2009-01-09       Impact factor: 24.633

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7.  SOX7-enforced expression promotes the expansion of adult blood progenitors and blocks B-cell development.

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8.  B-1 cells and B-1 cell precursors prompt different responses to Wnt signaling.

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