Literature DB >> 23351993

Animal models of human granulocyte diseases.

Alejandro A Schäffer1, Christoph Klein.   

Abstract

In vivo animal models have proven very useful to the understanding of basic biologic pathways of the immune system, a prerequisite for the development of innovate therapies. This article addresses currently available models for defined human monogenetic defects of neutrophil granulocytes, including murine, zebrafish, and larger mammalian species. Strengths and weaknesses of each system are summarized, and clinical investigators may thus be inspired to develop further lines of research to improve diagnosis and therapy by use of the appropriate animal model system. Published by Elsevier Inc.

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Year:  2012        PMID: 23351993      PMCID: PMC3558998          DOI: 10.1016/j.hoc.2012.10.005

Source DB:  PubMed          Journal:  Hematol Oncol Clin North Am        ISSN: 0889-8588            Impact factor:   3.722


  103 in total

1.  Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport.

Authors:  Juha Kolehmainen; Graeme C M Black; Anne Saarinen; Kate Chandler; Jill Clayton-Smith; Ann-Liz Träskelin; Rahat Perveen; Satu Kivitie-Kallio; Reijo Norio; Mette Warburg; Jean-Pierre Fryns; Albert de la Chapelle; Anna-Elina Lehesjoki
Journal:  Am J Hum Genet       Date:  2003-05-02       Impact factor: 11.025

2.  Intrinsic requirement for zinc finger transcription factor Gfi-1 in neutrophil differentiation.

Authors:  Hanno Hock; Melanie J Hamblen; Heather M Rooke; David Traver; Roderick T Bronson; Scott Cameron; Stuart H Orkin
Journal:  Immunity       Date:  2003-01       Impact factor: 31.745

3.  The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter.

Authors:  K Lühn; M K Wild; M Eckhardt; R Gerardy-Schahn; D Vestweber
Journal:  Nat Genet       Date:  2001-05       Impact factor: 38.330

4.  Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency.

Authors:  T Lübke; T Marquardt; A Etzioni; E Hartmann; K von Figura; C Körner
Journal:  Nat Genet       Date:  2001-05       Impact factor: 38.330

5.  IFN-gamma is effective in reducing infections in the mouse model of chronic granulomatous disease (CGD).

Authors:  S H Jackson; G F Miller; B H Segal; M Mardiney; J B Domachowske; J I Gallin; S M Holland
Journal:  J Interferon Cytokine Res       Date:  2001-08       Impact factor: 2.607

6.  Mice expressing a neutrophil elastase mutation derived from patients with severe congenital neutropenia have normal granulopoiesis.

Authors:  David S Grenda; Sonja E Johnson; Jill R Mayer; Morgan L McLemore; Kathleen F Benson; Marshall Horwitz; Daniel C Link
Journal:  Blood       Date:  2002-11-01       Impact factor: 22.113

7.  Inflammatory reactions and severe neutropenia in mice lacking the transcriptional repressor Gfi1.

Authors:  Holger Karsunky; Hui Zeng; Thorsten Schmidt; Branko Zevnik; Reinhart Kluge; Kurt Werner Schmid; Ulrich Dührsen; Tarik Möröy
Journal:  Nat Genet       Date:  2002-01-28       Impact factor: 38.330

8.  Mutations in proto-oncogene GFI1 cause human neutropenia and target ELA2.

Authors:  Richard E Person; Feng-Qian Li; Zhijun Duan; Kathleen F Benson; Jeremy Wechsler; Helen A Papadaki; George Eliopoulos; Christina Kaufman; Salvatore J Bertolone; Betty Nakamoto; Thalia Papayannopoulou; H Leighton Grimes; Marshall Horwitz
Journal:  Nat Genet       Date:  2003-07       Impact factor: 38.330

9.  Mutations associated with neutropenia in dogs and humans disrupt intracellular transport of neutrophil elastase.

Authors:  Kathleen F Benson; Feng-Qian Li; Richard E Person; Dalila Albani; Zhijun Duan; Jeremy Wechsler; Kimberly Meade-White; Kayleen Williams; Gregory M Acland; Glenn Niemeyer; Clinton D Lothrop; Marshall Horwitz
Journal:  Nat Genet       Date:  2003-08-03       Impact factor: 38.330

10.  Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease.

Authors:  Paolo A Hernandez; Robert J Gorlin; John N Lukens; Shoichiro Taniuchi; Joze Bohinjec; Fleur Francois; Mary E Klotman; George A Diaz
Journal:  Nat Genet       Date:  2003-05       Impact factor: 38.330

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  4 in total

1.  Constitutive activation of WASp in X-linked neutropenia renders neutrophils hyperactive.

Authors:  Marton Keszei; Julien Record; Joanna S Kritikou; Hannah Wurzer; Chiara Geyer; Meike Thiemann; Paul Drescher; Hanna Brauner; Laura Köcher; Jaime James; Minghui He; Marisa Ap Baptista; Carin Im Dahlberg; Amlan Biswas; David P Lane; Wenxia Song; Katrin Pütsep; Peter Vandenberghe; Scott B Snapper; Lisa S Westerberg
Journal:  J Clin Invest       Date:  2018-08-20       Impact factor: 14.808

Review 2.  Rare Genetic Blood Disease Modeling in Zebrafish.

Authors:  Alberto Rissone; Shawn M Burgess
Journal:  Front Genet       Date:  2018-08-31       Impact factor: 4.599

Review 3.  Granule protein processing and regulated secretion in neutrophils.

Authors:  Avinash Sheshachalam; Nutan Srivastava; Troy Mitchell; Paige Lacy; Gary Eitzen
Journal:  Front Immunol       Date:  2014-09-19       Impact factor: 7.561

Review 4.  Congenital defects in neutrophil dynamics.

Authors:  Marton Keszei; Lisa S Westerberg
Journal:  J Immunol Res       Date:  2014-08-05       Impact factor: 4.818

  4 in total

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