Literature DB >> 16304055

Keratinocyte growth factor (KGF) is required for postnatal thymic regeneration.

Onder Alpdogan1, Vanessa M Hubbard, Odette M Smith, Neel Patel, Sydney Lu, Gabrielle L Goldberg, Daniel H Gray, Jared Feinman, Adam A Kochman, Jeffrey M Eng, David Suh, Stephanie J Muriglan, Richard L Boyd, Marcel R M van den Brink.   

Abstract

Keratinocyte growth factor (KGF) is a member of the fibroblast growth factor family that mediates epithelial cell proliferation and differentiation in a variety of tissues, including the thymus. We studied the role of KGF in T-cell development with KGF-/- mice and demonstrated that thymic cellularity and the distribution of thymocyte subsets among KGF-/-, wildtype (WT), and KGF+/- mice were similar. However, KGF-/- mice are more vulnerable to sublethal irradiation (450 cGy), and a significant decrease was found in thymic cellularity after irradiation. Defective thymopoiesis and peripheral T-cell reconstitution were found in KGF-/- recipients of syngeneic or allogeneic bone marrow transplant, but using KGF-/- mice as a donor did not affect T-cell development after transplantation. Despite causing an early developmental block in the thymus, administration of KGF to young and old mice enhanced thymopoiesis. Exogenous KGF also accelerated thymic recovery after irradiation, cyclophosphamide, and dexamethasone treatment. Finally, we found that administering KGF before bone marrow transplantation (BMT) resulted in enhanced thymopoiesis and peripheral T-cell numbers in middle-aged recipients of an allogeneic BM transplant. We conclude that KGF plays a critical role in postnatal thymic regeneration and may be useful in treating immune deficiency conditions.

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Year:  2005        PMID: 16304055      PMCID: PMC1895735          DOI: 10.1182/blood-2005-07-2831

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  44 in total

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Authors:  R Boismenu; W L Havran
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Journal:  Science       Date:  1989-08-18       Impact factor: 47.728

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Journal:  Genes Dev       Date:  1996-01-15       Impact factor: 11.361

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Authors:  P W Finch; G R Cunha; J S Rubin; J Wong; D Ron
Journal:  Dev Dyn       Date:  1995-06       Impact factor: 3.780

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Review 3.  Adoptive precursor cell therapy to enhance immune reconstitution after hematopoietic stem cell transplantation.

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4.  Delayed immune reconstitution after cord blood transplantation is characterized by impaired thymopoiesis and late memory T-cell skewing.

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Review 5.  Clinical strategies to enhance T cell reconstitution.

Authors:  Gabrielle L Goldberg; Johannes L Zakrzewski; Miguel A Perales; Marcel R M van den Brink
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7.  FGF7 is a functional niche signal required for stimulation of adult liver progenitor cells that support liver regeneration.

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8.  Human proT-cells generated in vitro facilitate hematopoietic stem cell-derived T-lymphopoiesis in vivo and restore thymic architecture.

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9.  Short-term inhibition of p53 combined with keratinocyte growth factor improves thymic epithelial cell recovery and enhances T-cell reconstitution after murine bone marrow transplantation.

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Journal:  Blood       Date:  2009-12-04       Impact factor: 22.113

Review 10.  Rejuvenation of the aging T cell compartment.

Authors:  Amanda M Holland; Marcel R M van den Brink
Journal:  Curr Opin Immunol       Date:  2009-07-14       Impact factor: 7.486

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