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Quantification of collagen I in airway tissues using second harmonic generation.
Tjin, Gavin; Xu, Paul; Kable, Scott H; Kable, Eleanor P W; Burgess, Janette K.
Afiliação
  • Tjin G; Woolcock Institute of Medical Research, Level 3 Cell Biology Lab, 431 Glebe Point Road, Glebe, New South Wales 2037, Sydney, AustraliabThe University of Sydney, Central Clinical School, Faculty of Medicine, New South Wales 2006, Sydney, Australia.
  • Xu P; The University of Sydney, Australian Centre for Microscopy and Microanalysis, Madsen Building F09, New South Wales 2006, Sydney, Australia.
  • Kable SH; The University of Sydney, School of Chemistry, New South Wales 2006, Australia.
  • Kable EP; The University of Sydney, Australian Centre for Microscopy and Microanalysis, Madsen Building F09, New South Wales 2006, Sydney, Australia.
  • Burgess JK; Woolcock Institute of Medical Research, Level 3 Cell Biology Lab, 431 Glebe Point Road, Glebe, New South Wales 2037, Sydney, AustraliabThe University of Sydney, Central Clinical School, Faculty of Medicine, New South Wales 2006, Sydney, AustraliaeThe Univ.
J Biomed Opt ; 19(3): 36005, 2014 Mar.
Article em En | MEDLINE | ID: mdl-24604535
ABSTRACT
Extracellular matrix (ECM) remodeling contributes to the pathogenic changes in chronic obstructive pulmonary disease (COPD) and is both complex and not well understood. Collagen I, a component of the ECM altered in COPD airways, has second harmonic generation (SHG) properties. The SHG signal is coherent, propagating both forward (F) (primarily organized/mature collagen fibrils) and backward (B) (primarily disorganized/immature collagen fibrils) parallel to the incident light. The F/B SHG ratio was used to determine the proportion of organized to disorganized collagen, with lower variation in F/B ratio between sampling regions within the same patient and between patients in the same disease group compared with analyzing F and B data alone. The F/B ratio was independent of laser power drift, regions analyzed within a tissue and tissue orientation during analysis. Using this method, we identified a significant difference in collagen organization in airway tissue between COPD and non diseased. We have developed a robust optimization and calibration methodology that will allow direct comparison of data obtained at different times and from multiple microscopes, which is directly adaptable for use with other tissue types. We report a powerful new tool for advancing our understanding of pathological ECM remodeling that may uncover new therapeutic targets in the future.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Processamento de Sinais Assistido por Computador / Colágeno Tipo I / Pulmão Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Processamento de Sinais Assistido por Computador / Colágeno Tipo I / Pulmão Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article