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Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
by
Roberts, Edward
, Nicholson, Andrew G.
, Carlin, Leo M.
, Gaboriau, David C. A.
, Lloyd, Clare M.
, Molyneaux, Philip L.
, Byrne, Adam J.
, Walker, Simone A.
, Kemp, Samuel V.
, Hewitt, Richard J.
, Traves, William J.
, Maher, Toby M.
, Lennon, Rachel
, Fercoq, Frédéric
, Rice, Alexandra
, Fresquet, Maryline
, Yates, Laura L.
, Puttur, Franz
in
13/106
/ 14/19
/ 14/63
/ 14/69
/ 38/77
/ 45/90
/ 631/80/84/750
/ 692/308/1426
/ 692/699/1785
/ 82/58
/ Alveolar Epithelial Cells
/ Alveoli
/ Basal cells
/ Biological Transport
/ Cell migration
/ Cell Movement
/ Epithelial cells
/ Epithelium
/ Extracellular Matrix
/ Fibroblasts
/ Fibrosis
/ Gene expression
/ Glycoproteins
/ Humanities and Social Sciences
/ Humans
/ Idiopathic Pulmonary Fibrosis
/ Keratin-5
/ Lung diseases
/ Lungs
/ Mass spectrometry
/ Mass spectroscopy
/ multidisciplinary
/ Osteonectin
/ Overexpression
/ Proteomics
/ Pulmonary fibrosis
/ Science
/ Science (multidisciplinary)
2023
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Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
by
Roberts, Edward
, Nicholson, Andrew G.
, Carlin, Leo M.
, Gaboriau, David C. A.
, Lloyd, Clare M.
, Molyneaux, Philip L.
, Byrne, Adam J.
, Walker, Simone A.
, Kemp, Samuel V.
, Hewitt, Richard J.
, Traves, William J.
, Maher, Toby M.
, Lennon, Rachel
, Fercoq, Frédéric
, Rice, Alexandra
, Fresquet, Maryline
, Yates, Laura L.
, Puttur, Franz
in
13/106
/ 14/19
/ 14/63
/ 14/69
/ 38/77
/ 45/90
/ 631/80/84/750
/ 692/308/1426
/ 692/699/1785
/ 82/58
/ Alveolar Epithelial Cells
/ Alveoli
/ Basal cells
/ Biological Transport
/ Cell migration
/ Cell Movement
/ Epithelial cells
/ Epithelium
/ Extracellular Matrix
/ Fibroblasts
/ Fibrosis
/ Gene expression
/ Glycoproteins
/ Humanities and Social Sciences
/ Humans
/ Idiopathic Pulmonary Fibrosis
/ Keratin-5
/ Lung diseases
/ Lungs
/ Mass spectrometry
/ Mass spectroscopy
/ multidisciplinary
/ Osteonectin
/ Overexpression
/ Proteomics
/ Pulmonary fibrosis
/ Science
/ Science (multidisciplinary)
2023
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Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
by
Roberts, Edward
, Nicholson, Andrew G.
, Carlin, Leo M.
, Gaboriau, David C. A.
, Lloyd, Clare M.
, Molyneaux, Philip L.
, Byrne, Adam J.
, Walker, Simone A.
, Kemp, Samuel V.
, Hewitt, Richard J.
, Traves, William J.
, Maher, Toby M.
, Lennon, Rachel
, Fercoq, Frédéric
, Rice, Alexandra
, Fresquet, Maryline
, Yates, Laura L.
, Puttur, Franz
in
13/106
/ 14/19
/ 14/63
/ 14/69
/ 38/77
/ 45/90
/ 631/80/84/750
/ 692/308/1426
/ 692/699/1785
/ 82/58
/ Alveolar Epithelial Cells
/ Alveoli
/ Basal cells
/ Biological Transport
/ Cell migration
/ Cell Movement
/ Epithelial cells
/ Epithelium
/ Extracellular Matrix
/ Fibroblasts
/ Fibrosis
/ Gene expression
/ Glycoproteins
/ Humanities and Social Sciences
/ Humans
/ Idiopathic Pulmonary Fibrosis
/ Keratin-5
/ Lung diseases
/ Lungs
/ Mass spectrometry
/ Mass spectroscopy
/ multidisciplinary
/ Osteonectin
/ Overexpression
/ Proteomics
/ Pulmonary fibrosis
/ Science
/ Science (multidisciplinary)
2023
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Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
Journal Article
Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
2023
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Overview
Aberrant expansion of KRT5
+
basal cells in the distal lung accompanies progressive alveolar epithelial cell loss and tissue remodelling during fibrogenesis in idiopathic pulmonary fibrosis (IPF). The mechanisms determining activity of KRT5
+
cells in IPF have not been delineated. Here, we reveal a potential mechanism by which KRT5
+
cells migrate within the fibrotic lung, navigating regional differences in collagen topography. In vitro, KRT5
+
cell migratory characteristics and expression of remodelling genes are modulated by extracellular matrix (ECM) composition and organisation. Mass spectrometry- based proteomics revealed compositional differences in ECM components secreted by primary human lung fibroblasts (HLF) from IPF patients compared to controls. Over-expression of ECM glycoprotein, Secreted Protein Acidic and Cysteine Rich (SPARC) in the IPF HLF matrix restricts KRT5
+
cell migration in vitro. Together, our findings demonstrate how changes to the ECM in IPF directly influence KRT5
+
cell behaviour and function contributing to remodelling events in the fibrotic niche.
Idiopathic pulmonary fibrosis has been associated with aberrant expansion of KRT5-expressing basal cells. Here the authors show how changes in the ECM glycoprotein SPARC restrict the movement of KRT5+ cells, affecting their retention within fibrotic tissue.
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