Mast cells are tissue-resident cells with important functions in allergy and inflammation. Pluripotential hematopoietic stem cells in the bone marrow give rise to committed mast cell progenitors that transit via the blood to tissues throughout the body, where they mature. Knowledge is limited about the factors that release mast cell progenitors from the bone marrow or recruit them to remote tissues. Mouse femoral bone marrow cells were cultured with IL-3 for 2 wk and a range of chemotactic agents were tested on the c-kit+ population. Cells were remarkably refractory and no chemotaxis was induced by any chemokines tested. However, supernatants from activated mature mast cells induced pronounced chemotaxis, with the active principle identified as leukotriene (LT) B4. Other activation products were inactive. LTB4 was highly chemotactic for 2-wk-old cells, but not mature cells, correlating with a loss of mRNA for the LTB4 receptor, BLT1. Immature cells also accumulated in vivo in response to intradermally injected LTB4. Furthermore, LTB4 was highly potent in attracting mast cell progenitors from freshly isolated bone marrow cell suspensions. Finally, LTB4 was a potent chemoattractant for human cord blood–derived immature, but not mature, mast cells. These results suggest an autocrine role for LTB4 in regulating tissue mast cell numbers.
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20 June 2005
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June 13 2005
Leukotriene B4, an activation product of mast cells, is a chemoattractant for their progenitors
Charlotte L. Weller,
Charlotte L. Weller
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
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Sarah J. Collington,
Sarah J. Collington
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
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Jeremy K. Brown,
Jeremy K. Brown
2Department of Veterinary Clinical Studies, University of Edinburgh, Easter Bush Veterinary Centre, Roslin, Midlothian, EH25 9RG, Scotland, UK
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Hugh R.P. Miller,
Hugh R.P. Miller
2Department of Veterinary Clinical Studies, University of Edinburgh, Easter Bush Veterinary Centre, Roslin, Midlothian, EH25 9RG, Scotland, UK
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Adam Al-Kashi,
Adam Al-Kashi
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
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Peter Clark,
Peter Clark
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
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Peter J. Jose,
Peter J. Jose
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
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Adele Hartnell,
Adele Hartnell
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
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Timothy J. Williams
Timothy J. Williams
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
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Charlotte L. Weller
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
Sarah J. Collington
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
Jeremy K. Brown
2Department of Veterinary Clinical Studies, University of Edinburgh, Easter Bush Veterinary Centre, Roslin, Midlothian, EH25 9RG, Scotland, UK
Hugh R.P. Miller
2Department of Veterinary Clinical Studies, University of Edinburgh, Easter Bush Veterinary Centre, Roslin, Midlothian, EH25 9RG, Scotland, UK
Adam Al-Kashi
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
Peter Clark
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
Peter J. Jose
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
Adele Hartnell
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
Timothy J. Williams
1Leukocyte Biology Section, Biomedical Sciences Division, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, England, UK
CORRESPONDENCE Timothy J. Williams: [email protected]
Abbreviations used: 5-LO, 5-lipoxygenase; ACN, acetonitrile; BMMC, BM-derived mast cell; CBMC, cord blood– derived mast cell; CMFDA, 5-chloromethylfluorescein diacetate; HSA, human serum albumin; i.d., intradermal; LT, leukotriene; mMCP, murine mast cell protease; SCF, stem cell factor.
A. Hartnell and T. Williams contributed equally to this work.
Received:
November 24 2004
Accepted:
May 04 2005
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2005
J Exp Med (2005) 201 (12): 1961–1971.
Article history
Received:
November 24 2004
Accepted:
May 04 2005
Citation
Charlotte L. Weller, Sarah J. Collington, Jeremy K. Brown, Hugh R.P. Miller, Adam Al-Kashi, Peter Clark, Peter J. Jose, Adele Hartnell, Timothy J. Williams; Leukotriene B4, an activation product of mast cells, is a chemoattractant for their progenitors . J Exp Med 20 June 2005; 201 (12): 1961–1971. doi: https://doi.org/10.1084/jem.20042407
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