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Eosinophilopoiesis in a murine model of allergic airway eosinophilia: involvement of bone marrow IL-5 and IL-5 receptor alpha

Tomaki, Masafumi, 1964 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för lungmedicin och allergologi,Institute of Internal Medicine, Dept of Respiratory Medicine/Allergology
Zhao, Lin-Ling, 1957 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för lungmedicin och allergologi,Institute of Internal Medicine, Dept of Respiratory Medicine/Allergology
Lundahl, J. (author)
Karolinska Institutet
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Sjöstrand, Margareta, 1947 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för lungmedicin och allergologi,Institute of Internal Medicine, Dept of Respiratory Medicine/Allergology
Jordana, M. (author)
Lindén, Anders, 1961 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för lungmedicin och allergologi,Institute of Internal Medicine, Dept of Respiratory Medicine/Allergology
O'Byrne, P. (author)
Lötvall, Jan, 1956 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för lungmedicin och allergologi,Institute of Internal Medicine, Dept of Respiratory Medicine/Allergology
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 (creator_code:org_t)
The American Association of Immunologists, 2000
2000
English.
In: Journal of immunology (Baltimore, Md.. - : The American Association of Immunologists. - 0022-1767 .- 1550-6606. ; 165:7, s. 4040-50
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The airway inflammation in asthma is dominated by eosinophils. The aim of this study was to elucidate the contribution of newly produced eosinophils in airway allergic inflammation and to determine mechanisms of any enhanced eosinophilopoiesis. OVA-sensitized BALB/c mice were repeatedly exposed to allergen via airway route. Newly produced cells were identified using a thymidine analog, 5-bromo-2'-deoxyuridine, which is incorporated into DNA during mitosis. Identification of IL-5-producing cells in the bone marrow was performed using FACS. Bone marrow CD3+ cells were enriched to evaluate IL-5-protein release in vitro. Anti-IL-5-treatment (TRFK-5) was given either systemically or directly to the airways. IL-5R-bearing cells were localized by immunocytochemistry. Repeated airway allergen exposure caused prominent airway eosinophilia after three to five exposures, and increased the number of immature eosinophils in the bone marrow. Up to 78% of bronchoalveolar lavage (BAL) granulocytes were 5-bromo-2'-deoxyuridine positive. After three allergen exposures, both CD3+ and non-CD3 cells acquired from the bone marrow expressed and released IL-5-protein. Anti-IL-5 given i.p. inhibited both bone marrow and airway eosinophilia. Intranasal administration of anti-IL-5 also reduced BAL eosinophilia, partly via local effects in the airways. Bone marrow cells, but not BAL eosinophils, displayed stainable amounts of the IL-5R alpha-chain. We conclude that the bone marrow is activated by airway allergen exposure, and that newly produced eosinophils contribute to a substantial degree to the airway eosinophilia induced by allergen. Airway allergen exposure increases the number of cells expressing IL-5-protein in the bone marrow. The bone marrow, as well as the lung, are possible targets for anti-IL-5-treatment.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)

Keyword

Administration
Intranasal
Allergens/administration & dosage/immunology
Animals
Antibodies
Monoclonal/administration & dosage
Bone Marrow Cells/chemistry/*immunology/pathology
Bromodeoxyuridine/administration & dosage/analysis
Bronchoalveolar Lavage Fluid/chemistry/immunology
Cell Movement/immunology
Coloring Agents/administration & dosage/analysis
Disease Models
Animal
Eosinophils/chemistry/*immunology/pathology
Granulocytes/chemistry/immunology/pathology
Hematopoiesis/*immunology
Hematopoietic Stem Cells/chemistry/immunology/pathology
Inflammation/immunology/pathology
Injections
Intraperitoneal
Interleukin-5/immunology/*physiology
Leukocyte Count
Male
Mice
Mice
Inbred BALB C
Ovalbumin/administration & dosage/immunology
Pulmonary Eosinophilia/*immunology/metabolism/pathology
Receptors
Interleukin/analysis/*physiology
Receptors
Interleukin-5
Time Factors

Publication and Content Type

ref (subject category)
art (subject category)

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