Collagen V-induced nasal tolerance downregulates pulmonary collagen mRNA gene and TGF-beta expression in experimental systemic sclerosis


Autoria(s): VELOSA, Ana Paula P.; TEODORO, Walcy R.; ANJOS, Daniel M. dos; KONNO, Renata; OLIVEIRA, Cristiane C.; KATAYAMA, Maria L. H.; PARRA, Edwin R.; CAPELOZZI, Vera L.; YOSHINARI, Natalino H.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/04/2012

18/04/2012

2010

Resumo

Background: The purpose of this study was to evaluate collagen deposition, mRNA collagen synthesis and TGFbeta expression in the lung tissue in an experimental model of scleroderma after collagen V-induced nasal tolerance. Methods: Female New Zealand rabbits (N = 12) were immunized with 1 mg/ml of collagen V in Freund's adjuvant (IM). After 150 days, six immunized animals were tolerated by nasal administration of collagen V ( 25 mu g/day) (IM-TOL) daily for 60 days. The collagen content was determined by morphometry, and mRNA expressions of types I, III and V collagen were determined by Real-time PCR. The TGF-beta expression was evaluated by immunostaining and quantified by point counting methods. To statistic analysis ANOVA with Bonferroni test were employed for multiple comparison when appropriate and the level of significance was determined to be p < 0.05. Results: IM-TOL, when compared to IM, showed significant reduction in total collagen content around the vessels (0.371 +/- 0.118 vs. 0.874 +/- 0.282, p < 0.001), bronchioles (0.294 +/- 0.139 vs. 0.646 +/- 0.172, p < 0.001) and in the septal interstitium (0.027 +/- 0.014 vs. 0.067 +/- 0.039, p = 0.026). The lung tissue of IM-TOL, when compared to IM, showed decreased immunostaining of types I, III and V collagen, reduced mRNA expression of types I (0.10 +/- 0.07 vs. 1.0 +/- 0.528, p = 0.002) and V (1.12 +/- 0.42 vs. 4.74 +/- 2.25, p = 0.009) collagen, in addition to decreased TGF-beta expression ( p < 0.0001). Conclusions: Collagen V-induced nasal tolerance in the experimental model of SSc regulated the pulmonary remodeling process, inhibiting collagen deposition and collagen I and V mRNA synthesis. Additionally, it decreased TGF-beta expression, suggesting a promising therapeutic option for scleroderma treatment.

State of Sao Paulo (FAPESP)

Laboratories for Medical Research (LIMs), University Hospital, School of Medicine, University of Sao Paulo (USP)

Federico Foundation

Identificador

RESPIRATORY RESEARCH, LONDON, v.11, JAN 4, 2010

1465-9921

http://producao.usp.br/handle/BDPI/15210

10.1186/1465-9921-11-1

http://dx.doi.org/10.1186/1465-9921-11-1

Idioma(s)

eng

Publicador

BIOMED CENTRAL LTD

LONDON

Relação

Respiratory Research

Direitos

openAccess

Copyright BIOMED CENTRAL LTD

Palavras-Chave #LUNG ALLOGRAFT-REJECTION #CONNECTIVE-TISSUE DISEASES #ORAL TOLERANCE #EXPERIMENTAL-MODEL #I COLLAGEN #T-CELLS #PATHOGENESIS #SCLERODERMA #AUTOIMMUNITY #IMMUNIZATION #Respiratory System
Tipo

article

original article

publishedVersion