Abstract | BACKGROUND:
Eotaxin-2/CCL24 and eotaxin-3/CCL26 play an important role in eosinophil chemotaxis and activation in asthma. We previously demonstrated that eotaxin/CCL11 is profibrogenic for human lung fibroblasts. The effect of eotaxin-2/ CCL24 and eotaxin-3/CCL26 on lung fibroblasts has not yet been investigated. OBJECTIVE: To evaluate whether eotaxin-2/CCL24 and eotaxin-3/CCL26 modulate fibrotic properties of lung fibroblasts. METHODS: Fibroblast proliferation was evaluated by means of 3-hydroxythymidine incorporation. Collagen production was assessed by means of 3-hydroxyproline incorporation and biochemical staining. Chemotaxis was determined using Boyden chambers. Expression of alpha-smooth muscle actin was evaluated by means of immunostaining. Transforming growth factor beta1 release was assessed using enzyme-linked immunosorbent assay. Parametric analysis of variance, followed by the Tukey-Kramer multiple comparisons test, was used to calculate statistical significance. RESULTS: CONCLUSIONS:
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Authors | Martin Kohan, Ilaria Puxeddu, Reuven Reich, Francesca Levi-Schaffer, Neville Berkman |
Journal | Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
(Ann Allergy Asthma Immunol)
Vol. 104
Issue 1
Pg. 66-72
(Jan 2010)
ISSN: 1081-1206 [Print] United States |
PMID | 20143648
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Actins
- CCL24 protein, human
- CCL26 protein, human
- Chemokine CCL24
- Chemokine CCL26
- Chemokines, CC
- Recombinant Proteins
- Transforming Growth Factor beta1
- Collagen
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Topics |
- Actins
(biosynthesis)
- Airway Remodeling
- Cell Differentiation
(drug effects)
- Cell Line
- Cell Proliferation
(drug effects)
- Chemokine CCL24
(pharmacology)
- Chemokine CCL26
- Chemokines, CC
(pharmacology)
- Chemotaxis
(drug effects)
- Collagen
(biosynthesis)
- Fibroblasts
(drug effects, metabolism, pathology)
- Humans
- Lung
(pathology)
- Pulmonary Fibrosis
(etiology, pathology)
- Recombinant Proteins
(pharmacology)
- Transforming Growth Factor beta1
(metabolism)
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