Your browser doesn't support javascript.
loading
Functional Pdgfra fibroblast heterogeneity in normal and fibrotic mouse lung.
Trempus, Carol S; Papas, Brian N; Sifre, Maria I; Bortner, Carl D; Scappini, Erica; Tucker, Charles J; Xu, Xin; Johnson, Katina L; Deterding, Leesa J; Williams, Jason G; Johnson, Dylan J; Li, Jian-Liang; Sutton, Deloris; Ganta, Charan; Mahapatra, Debabrata; Arif, Muhammad; Basu, Abhishek; Pommerolle, Lenny; Cinar, Resat; Perl, Anne K; Garantziotis, Stavros.
Afiliación
  • Trempus CS; Immunity, Inflammation, and Disease Laboratory.
  • Papas BN; Biostatistics & Computational Biology Branch.
  • Sifre MI; Signal Transduction Laboratory, and.
  • Bortner CD; Signal Transduction Laboratory, and.
  • Scappini E; Signal Transduction Laboratory, and.
  • Tucker CJ; Signal Transduction Laboratory, and.
  • Xu X; Epigenetics & Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, North Carolina, USA.
  • Johnson KL; Epigenetics & Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, North Carolina, USA.
  • Deterding LJ; Epigenetics & Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, North Carolina, USA.
  • Williams JG; Epigenetics & Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, North Carolina, USA.
  • Johnson DJ; Biostatistics & Computational Biology Branch.
  • Li JL; Biostatistics & Computational Biology Branch.
  • Sutton D; Comparative & Molecular Pathogenesis Branch, National Institute of Environmental Health Sciences, Division of Translational Toxicology, Research Triangle Park, North Carolina, USA.
  • Ganta C; Comparative & Molecular Pathogenesis Branch, National Institute of Environmental Health Sciences, Division of Translational Toxicology, Research Triangle Park, North Carolina, USA.
  • Mahapatra D; Inotiv, Research Triangle Park, North Carolina, USA.
  • Arif M; Inotiv, Research Triangle Park, North Carolina, USA.
  • Basu A; Section on Fibrotic Disorders, and.
  • Pommerolle L; Laboratory of Cardiovascular Physiology and Tissue Injury, National Institute on Alcohol Abuse and Alcoholism, NIH, Rockville, Maryland, USA.
  • Cinar R; Section on Fibrotic Disorders, and.
  • Perl AK; Section on Fibrotic Disorders, and.
  • Garantziotis S; Section on Fibrotic Disorders, and.
JCI Insight ; 8(22)2023 Nov 22.
Article en En | MEDLINE | ID: mdl-37824216
Aberrant fibroblast function plays a key role in the pathogenesis of idiopathic pulmonary fibrosis, a devastating disease of unrelenting extracellular matrix deposition in response to lung injury. Platelet-derived growth factor α-positive (Pdgfra+) lipofibroblasts (LipoFBs) are essential for lung injury response and maintenance of a functional alveolar stem cell niche. Little is known about the effects of lung injury on LipoFB function. Here, we used single-cell RNA-Seq (scRNA-Seq) technology and PdgfraGFP lineage tracing to generate a transcriptomic profile of Pdgfra+ fibroblasts in normal and injured mouse lungs 14 days after bleomycin exposure, generating 11 unique transcriptomic clusters that segregated according to treatment. While normal and injured LipoFBs shared a common gene signature, injured LipoFBs acquired fibrogenic pathway activity with an attenuation of lipogenic pathways. In a 3D organoid model, injured Pdgfra+ fibroblast-supported organoids were morphologically distinct from those cultured with normal fibroblasts, and scRNA-Seq analysis suggested distinct transcriptomic changes in alveolar epithelia supported by injured Pdgfra+ fibroblasts. In summary, while LipoFBs in injured lung have not migrated from their niche and retain their lipogenic identity, they acquire a potentially reversible fibrogenic profile, which may alter the kinetics of epithelial regeneration and potentially contribute to dysregulated repair, leading to fibrosis.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrosis Pulmonar Idiopática / Lesión Pulmonar Límite: Animals Idioma: En Revista: JCI Insight Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrosis Pulmonar Idiopática / Lesión Pulmonar Límite: Animals Idioma: En Revista: JCI Insight Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos