Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Regional and disease specific human lung extracellular matrix composition

Hoffman, Evan T. ; Uhl, Franziska E. LU ; Asarian, Loredana ; Deng, Bin ; Becker, Chloe ; Uriarte, Juan J. ; Downs, Isaac ; Young, Brad and Weiss, Daniel J. (2023) In Biomaterials 293.
Abstract

Chronic lung diseases, such as chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF), are characterized by regional extracellular matrix (ECM) remodeling which contributes to disease progression. Previous proteomic studies on whole decellularized lungs have provided detailed characterization on the impact of COPD and IPF on total lung ECM composition. However, such studies are unable to determine the differences in ECM composition between individual anatomical regions of the lung. Here, we employ a post-decellularization dissection method to compare the ECM composition of whole decellularized lungs (wECM) and specific anatomical lung regions, including alveolar-enriched ECM (aECM), airway ECM (airECM), and... (More)

Chronic lung diseases, such as chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF), are characterized by regional extracellular matrix (ECM) remodeling which contributes to disease progression. Previous proteomic studies on whole decellularized lungs have provided detailed characterization on the impact of COPD and IPF on total lung ECM composition. However, such studies are unable to determine the differences in ECM composition between individual anatomical regions of the lung. Here, we employ a post-decellularization dissection method to compare the ECM composition of whole decellularized lungs (wECM) and specific anatomical lung regions, including alveolar-enriched ECM (aECM), airway ECM (airECM), and vasculature ECM (vECM), between non-diseased (ND), COPD, and IPF human lungs. We demonstrate, using mass spectrometry, that individual regions possess a unique ECM signature characterized primarily by differences in collagen composition and basement-membrane associated proteins, including ECM glycoproteins. We further demonstrate that both COPD and IPF lead to alterations in lung ECM composition in a region-specific manner, including enrichment of type-III collagen and fibulin in IPF aECM. Taken together, this study provides methodology for future studies, including isolation of region-specific lung biomaterials, as well as a dataset that may be applied for the identification of novel ECM targets for therapeutics.

(Less)
Please use this url to cite or link to this publication:
author
; ; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Decellularization, Extracellular matrix, Lung, Proteomics
in
Biomaterials
volume
293
article number
121960
publisher
Elsevier
external identifiers
  • pmid:36580718
  • scopus:85144817689
ISSN
0142-9612
DOI
10.1016/j.biomaterials.2022.121960
language
English
LU publication?
yes
id
e13045db-777f-42db-9f8c-e35aa612a2f7
date added to LUP
2023-02-02 09:47:05
date last changed
2024-11-01 01:09:24
@article{e13045db-777f-42db-9f8c-e35aa612a2f7,
  abstract     = {{<p>Chronic lung diseases, such as chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF), are characterized by regional extracellular matrix (ECM) remodeling which contributes to disease progression. Previous proteomic studies on whole decellularized lungs have provided detailed characterization on the impact of COPD and IPF on total lung ECM composition. However, such studies are unable to determine the differences in ECM composition between individual anatomical regions of the lung. Here, we employ a post-decellularization dissection method to compare the ECM composition of whole decellularized lungs (wECM) and specific anatomical lung regions, including alveolar-enriched ECM (aECM), airway ECM (airECM), and vasculature ECM (vECM), between non-diseased (ND), COPD, and IPF human lungs. We demonstrate, using mass spectrometry, that individual regions possess a unique ECM signature characterized primarily by differences in collagen composition and basement-membrane associated proteins, including ECM glycoproteins. We further demonstrate that both COPD and IPF lead to alterations in lung ECM composition in a region-specific manner, including enrichment of type-III collagen and fibulin in IPF aECM. Taken together, this study provides methodology for future studies, including isolation of region-specific lung biomaterials, as well as a dataset that may be applied for the identification of novel ECM targets for therapeutics.</p>}},
  author       = {{Hoffman, Evan T. and Uhl, Franziska E. and Asarian, Loredana and Deng, Bin and Becker, Chloe and Uriarte, Juan J. and Downs, Isaac and Young, Brad and Weiss, Daniel J.}},
  issn         = {{0142-9612}},
  keywords     = {{Decellularization; Extracellular matrix; Lung; Proteomics}},
  language     = {{eng}},
  publisher    = {{Elsevier}},
  series       = {{Biomaterials}},
  title        = {{Regional and disease specific human lung extracellular matrix composition}},
  url          = {{http://dx.doi.org/10.1016/j.biomaterials.2022.121960}},
  doi          = {{10.1016/j.biomaterials.2022.121960}},
  volume       = {{293}},
  year         = {{2023}},
}