Literature DB >> 34595313

Generation of Busulfan Chimeric Mice for the Analysis of T Cell Population Dynamics.

Thea Hogan1, Andrew Yates2,3, Benedict Seddon1.   

Abstract

This protocol was developed to generate chimeric mice in which T lymphocytes could be stratified by age on the basis of congenic marker expression. The conditioning drug busulfan is used to ablate host haematopoietic stem cells while leaving the peripheral immune system intact. Busulfan treatment is followed by bone marrow transplantation (BMT), with T-cell depleted donor bone marrow bearing a different congenic marker (CD45.2) to that of the host mouse (CD45.1). New cell production post-BMT can thus be tracked by measuring the fraction of CD45.2+ cells over time within a population of interest ( Hogan et al., 2015 ; Gossel et al., 2017 ).
Copyright © The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Bone marrow chimeras; Busulfan; T cell homeostasis; T cells; Temporal fate mapping

Year:  2017        PMID: 34595313      PMCID: PMC8438465          DOI: 10.21769/BioProtoc.2650

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  6 in total

Review 1.  Immune reconstitution following hematopoietic progenitor cell transplantation: challenges for the future.

Authors:  T J Fry; C L Mackall
Journal:  Bone Marrow Transplant       Date:  2005-03       Impact factor: 5.483

2.  Comparison of different busulfan analogues for depletion of hematopoietic stem cells and promotion of donor-type chimerism in murine bone marrow transplant recipients.

Authors:  G R Westerhof; R E Ploemacher; A Boudewijn; I Blokland; J H Dillingh; A T McGown; J A Hadfield; M J Dawson; J D Down
Journal:  Cancer Res       Date:  2000-10-01       Impact factor: 12.701

3.  Low-dose parenteral busulfan provides an extended window for the infusion of hematopoietic stem cells in murine hosts.

Authors:  Matthew M Hsieh; Saskia Langemeijer; Aisha Wynter; Oswald A Phang; Elizabeth M Kang; John F Tisdale
Journal:  Exp Hematol       Date:  2007-07-09       Impact factor: 3.084

4.  The molecular program induced in T cells undergoing homeostatic proliferation.

Authors:  Ananda W Goldrath; C John Luckey; Richard Park; Christophe Benoist; Diane Mathis
Journal:  Proc Natl Acad Sci U S A       Date:  2004-11-17       Impact factor: 11.205

5.  Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels.

Authors:  Graeme Gossel; Thea Hogan; Benedict Seddon; Andrew J Yates; Daniel Cownden
Journal:  Elife       Date:  2017-03-10       Impact factor: 8.140

6.  Temporal fate mapping reveals age-linked heterogeneity in naive T lymphocytes in mice.

Authors:  Thea Hogan; Graeme Gossel; Andrew J Yates; Benedict Seddon
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-25       Impact factor: 11.205

  6 in total
  2 in total

Review 1.  Fate-mapping mice: new tools and technology for immune discovery.

Authors:  Scarlett E Lee; Brian D Rudd; Norah L Smith
Journal:  Trends Immunol       Date:  2022-01-31       Impact factor: 16.687

2.  Towards a unified model of naive T cell dynamics across the lifespan.

Authors:  Sanket Rane; Thea Hogan; Edward Lee; Benedict Seddon; Andrew J Yates
Journal:  Elife       Date:  2022-06-09       Impact factor: 8.713

  2 in total

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