Mast cell-derived tumour necrosis factor is essential for allergic airway disease

被引:66
|
作者
Reuter, S. [1 ]
Heinz, A. [1 ]
Sieren, M. [1 ]
Wiewrodt, R. [1 ]
Gelfand, E. W. [3 ]
Stassen, M. [2 ]
Buhl, R. [1 ]
Taube, C. [1 ,3 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Pulm Med, Med Clin 3, D-55101 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Inst Immunol, D-6500 Mainz, Germany
[3] Natl Jewish Med & Res Ctr, Div Cell Biol, Dept Paediat, Denver, CO USA
关键词
asthma; immunology; mast cell; tumour necrosis factor;
D O I
10.1183/09031936.00058907
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Mast cells are thought to contribute to allergic airway disease. However, the role of mast cell-produced mediators, such as tumour necrosis factor (TNF), for the development of allergic airway disease is unclear. In order to define the role of mast cells in acute allergic airway disease two strains of mast cell-deficient mice (Kitw/wv and KitW-shiW-sh) were studied. Compared with their wild-type littermates, Kitw/wv and KitW-sh/W-sh mice developed significantly lower airway responsiveness to methacholine and less airway inflammation and goblet cell metaplasia, following sensitisation in the absence of adjuvant and airway challenge. Transfer of bone marrow-derived mast cells (BMMCs) from wild-type mice to KitW-sh/W-sh mice reconstituted both airway responsiveness and inflammation to levels similar to those in sensitised and challenged wild-type mice. In contrast, sensitised KitW-sh/W-sh mice reconstituted with BMMCs from TNF-deficient mice were still severely impaired in their ability to develop airway hyperresponsiveness, inflammation or goblet cell metaplasia following allergen challenge. The present results demonstrate the significance of mast cells in the development of airway disease and highlight the importance of mast cell-derived tumour necrosis factor in these responses.
引用
收藏
页码:773 / 782
页数:10
相关论文
共 50 条
  • [1] Critical protective role of mast cell-derived tumour necrosis factor in bacterial infection
    Mannel, DN
    Hultner, L
    Echtenacher, B
    [J]. RESEARCH IN IMMUNOLOGY, 1996, 147 (8-9): : 491 - 493
  • [2] T cell-derived tumour necrosis factor is essential, but not sufficient, for protection against Mycobacterium tuberculosis infection
    Saunders, BM
    Briscoe, H
    Britton, WJ
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2004, 137 (02): : 279 - 287
  • [3] Protective roles of mast cell-derived tumor necrosis factor in murine malaria
    Watanabe, N.
    Kikuchi, T.
    Iwakura, Y.
    Kawazu, S.
    Kano, S.
    Furuta, T.
    [J]. ICOPA XI: PROCEEDINGS OF THE 11TH INTERNATIONAL CONGRESS OF PARASITOLOGY, 2006, : 637 - +
  • [4] Dendritic Cell-Derived Tumor Necrosis Factor α Modifies Airway Epithelial Cell Responses
    Lutfi, R.
    Ledford, J. R.
    Zhou, P.
    Lewkowich, I. P.
    Page, K.
    [J]. JOURNAL OF INNATE IMMUNITY, 2012, 4 (5-6) : 542 - 552
  • [5] THE ROLE OF MAST CELL-DERIVED MEDIATORS IN AIRWAY FUNCTION
    LAZARUS, SC
    [J]. AMERICAN REVIEW OF RESPIRATORY DISEASE, 1987, 135 (06): : S35 - S38
  • [6] Mast cell-derived histamine and tumour necrosis factor: Differences between SJL/J and BALB/c inbred strains of mice
    Bebo, BF
    Lee, CH
    Orr, EL
    Linthicum, DS
    [J]. IMMUNOLOGY AND CELL BIOLOGY, 1996, 74 (03): : 225 - 230
  • [7] Mast cell-derived tumour necrosis factor-α mediates macrophage inflammatory protein-2-induced recruitment of neutrophils in mice
    Wang, YS
    Thorlacius, H
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2005, 145 (08) : 1062 - 1068
  • [8] Immunomodulatory Effects of Mesenchymal Stem Cell-Derived Extracellular Vesicles in Allergic Airway Disease
    Kim, Sung-Dong
    Cho, Kyu-Sup
    [J]. LIFE-BASEL, 2022, 12 (12):
  • [9] Mast cell-derived endothelin-1 contributes to allergic inflammation
    Metz, M.
    Schaefer, B.
    Tsai, M.
    Galli, S. J.
    Maurer, M.
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2007, 127 : S1 - S1
  • [10] Mast cell-derived tumor necrosis factor induces hypertrophy of draining lymph nodes during infection
    McLachlan, JB
    Hart, JP
    Pizzo, SV
    Shelburne, CP
    Staats, HF
    Gunn, MD
    Abraham, SN
    [J]. NATURE IMMUNOLOGY, 2003, 4 (12) : 1199 - 1205