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Precursor B Cells Increase in the Lung during Airway Allergic Inflammation: A Role for B Cell-Activating Factor

Samitas, Konstantinos, 1977 (author)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Malmhäll, Carina, 1959 (author)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Rådinger, Madeleine, 1967 (author)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
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Ramos-Ramírez, Patricia (author)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Lu, You, 1982 (author)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Deák, Tünde, 1983 (author)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Semitekolou, M. (author)
Gaga, M. (author)
Sjöstrand, Margareta, 1947 (author)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Lötvall, Jan, 1956 (author)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Bossios, Apostolos, 1969 (author)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
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 (creator_code:org_t)
2016-08-11
2016
English.
In: Plos One. - : Public Library of Science (PLoS). - 1932-6203. ; 11:8
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background B cells, key cells in allergic inflammation, differentiate in the bone marrow and their precursors include pro-B, pre-B and immature B cells. Eosinophil progenitor cells increase in the lung after allergen exposure. However, the existence and possible role of B cell precursors in the lung during allergic inflammation remains elusive. A BALB/c mouse model of allergic airway inflammation was utilized to perform phenotypic and quantification analyses of pro-B and pre-B cells in the lung by flow cytometry. B cell maturation factors IL-7 and B cell-activating factor (BAFF) and their receptors (CD127 and BAFFR, BCMA, TACI, respectively) were also evaluated in the lung and serum. The effect of anti-BAFF treatment was investigated both in vivo (i.p. administration of BAFF-R-Ig fusion protein) and in vitro (colony forming cell assay). Finally, BAFF levels were examined in the bronchoalveolar lavage (BAL) of asthmatic patients and healthy controls. Precursor pro and pre-B cells increase in the lung after allergen exposure, proliferate in the lung tissue in vivo, express markers of chemotaxis (CCR10 and CXCR4) and co-stimulation (CD40, CD86) and are resistant to apoptosis (Bax). Precursor B cells express receptors for BAFF at baseline, while after allergen challenge both their ligand BAFF and the BCMA receptor expression increases in B cell precursors. Blocking BAFFR in the lung in vivo decreases eosinophils and proliferating precursor B cells. Blocking BAFFR in bone marrow cultures in vitro reduces pre-B colony formation units. BAFF is increased in the BAL of severe asthmatics. Our data support the concept of a BAFF-mediated role for B cell precursors in allergic airway inflammation.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Keyword

bone-marrow
eosinophil progenitors
ccr10 expression
secreting cells
factor baff
asthma
survival
mice
differentiation
proliferation
Science & Technology - Other Topics

Publication and Content Type

ref (subject category)
art (subject category)

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