GDF15 is an epithelial-derived biomarker of idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is the most common and devastating of the interstitial lung diseases. Epithelial dysfunction is thought to play a prominent role in disease pathology, and we sought to characterize secreted signals that may contribute to disease pathology. Transcriptional profiling of senescent type II alveolar epithelial cells from mice with epithelial-specific telomere dysfunction identified the transforming growth factor-β family member, growth and differentiation factor 15 (Gdf15), as the most significantly upregulated secreted protein. Gdf15 expression is induced in response to telomere dysfunction and bleomycin challenge in mice. Gdf15 mRNA is expressed by lung epithelial cells, and protein can be detected in peripheral blood and bronchoalveolar lavage following bleomycin challenge in mice. In patients with IPF, GDF15 mRNA expression in lung tissue is significantly increased and correlates with pulmonary function. Single-cell RNA sequencing of human lungs identifies epithelial cells as the primary source of GDF15, and circulating concentrations of GDF15 are markedly elevated and correlate with disease severity and survival in multiple independent cohorts. Our findings suggest that GDF15 is an epithelial-derived secreted protein that may be a useful biomarker of epithelial stress and identifies IPF patients with poor outcomes.

[1]  P. Benos,et al.  Proliferating SPP1/MERTK-expressing macrophages in idiopathic pulmonary fibrosis , 2019, European Respiratory Journal.

[2]  A. Shilatifard,et al.  Single-Cell Transcriptomic Analysis of Human Lung Provides Insights into the Pathobiology of Pulmonary Fibrosis , 2019, American journal of respiratory and critical care medicine.

[3]  J. Curtis,et al.  GDF-15 in Pulmonary and Critical Care Medicine. , 2019, American journal of respiratory cell and molecular biology.

[4]  Christopher R. Cabanski,et al.  Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study. , 2018, The Lancet. Respiratory medicine.

[5]  A. Moore,et al.  Plasma proteomic signature of age in healthy humans , 2018, Aging cell.

[6]  S. Blankenberg,et al.  Biomarkers for heart failure: small molecules with high clinical relevance , 2018, Journal of internal medicine.

[7]  M. Dimopoulos,et al.  Growth differentiation factor-15 is a new biomarker for survival and renal outcomes in light chain amyloidosis. , 2018, Blood.

[8]  Jeong Hwan Park,et al.  Growth differentiation factor 15 predicts advanced fibrosis in biopsy‐proven non‐alcoholic fatty liver disease , 2018, Liver international : official journal of the International Association for the Study of the Liver.

[9]  T. Eling,et al.  Overproduction of growth differentiation factor 15 promotes human rhinovirus infection and virus-induced inflammation in the lung. , 2018, American journal of physiology. Lung cellular and molecular physiology.

[10]  Margaret A. Strong,et al.  Diagnostic utility of telomere length testing in a hospital-based setting , 2018, Proceedings of the National Academy of Sciences.

[11]  C. D. Dela Cruz,et al.  Extracellular Mitochondrial DNA Is Generated by Fibroblasts and Predicts Death in Idiopathic Pulmonary Fibrosis , 2017, American journal of respiratory and critical care medicine.

[12]  Jie Tang,et al.  Non-homeostatic body weight regulation through a brainstem-restricted receptor for GDF15 , 2017, Nature.

[13]  A. Kamal,et al.  Growth Differentiation Factor-15 (GDF-15) Level and Relation to Clinical Manifestations in Egyptian Systemic Sclerosis patients: Preliminary Data , 2017, Immunological investigations.

[14]  Søren B. Padkjær,et al.  GFRAL is the receptor for GDF15 and is required for the anti-obesity effects of the ligand , 2017, Nature Medicine.

[15]  P. Emmerson,et al.  The metabolic effects of GDF15 are mediated by the orphan receptor GFRAL , 2017, Nature Medicine.

[16]  T. Cash-Mason,et al.  GFRAL is the receptor for GDF15 and the ligand promotes weight loss in mice and nonhuman primates , 2017, Nature Medicine.

[17]  D. Goldstein,et al.  An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis , 2017, American journal of respiratory and critical care medicine.

[18]  J. Guiot,et al.  Blood Biomarkers in Idiopathic Pulmonary Fibrosis , 2017, Lung.

[19]  P. Bakke,et al.  Growth differentiation factor-15 is a predictor of important disease outcomes in patients with COPD , 2017, European Respiratory Journal.

[20]  E. Regan,et al.  GDF-15 plasma levels in chronic obstructive pulmonary disease are associated with subclinical coronary artery disease , 2017, Respiratory Research.

[21]  G. Joos,et al.  Elevated GDF-15 contributes to pulmonary inflammation upon cigarette smoke exposure , 2017, Mucosal Immunology.

[22]  Hyun Jin Kim,et al.  Growth Differentiation Factor 15 Predicts Chronic Liver Disease Severity , 2016, Gut and liver.

[23]  B. Stripp,et al.  Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis. , 2016, JCI insight.

[24]  D. Schwartz,et al.  Pulmonary fibrosis in the era of stratified medicine , 2016, Thorax.

[25]  J. Tedrow,et al.  Expression of RXFP1 Is Decreased in Idiopathic Pulmonary Fibrosis. Implications for Relaxin-based Therapies. , 2016, American journal of respiratory and critical care medicine.

[26]  S. Butz,et al.  GDF-15 inhibits integrin activation and mouse neutrophil recruitment through the ALK-5/TGF-βRII heterodimer. , 2016, Blood.

[27]  K. Lingappan,et al.  Role of GDF15 (growth and differentiation factor 15) in pulmonary oxygen toxicity. , 2015, Toxicology in vitro : an international journal published in association with BIBRA.

[28]  Meilan K. Han,et al.  Acute exacerbations of chronic obstructive pulmonary disease are associated with decreased CD4+ & CD8+ T cells and increased growth & differentiation factor-15 (GDF-15) in peripheral blood , 2015, Respiratory Research.

[29]  S. E. Stanley,et al.  Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis. , 2015, Chest.

[30]  S. E. Stanley,et al.  Telomere dysfunction causes alveolar stem cell failure , 2015, Proceedings of the National Academy of Sciences.

[31]  S. Mane,et al.  Exome Sequencing Links Mutations in PARN and RTEL1 with Familial Pulmonary Fibrosis and Telomere Shortening , 2015, Nature Genetics.

[32]  Zhongming Zhao,et al.  Rare variants in RTEL1 are associated with familial interstitial pneumonia. , 2015, American journal of respiratory and critical care medicine.

[33]  J. Hoeijmakers,et al.  An essential role for senescent cells in optimal wound healing through secretion of PDGF-AA. , 2014, Developmental cell.

[34]  Shin‐Yup Lee,et al.  Prognostic Value of Serum Growth Differentiation Factor-15 in Patients with Chronic Obstructive Pulmonary Disease Exacerbation , 2014, Tuberculosis and respiratory diseases.

[35]  D. Deforce,et al.  Growth Differentiation Factor 15, a Marker of Lung Involvement in Systemic Sclerosis, Is Involved in Fibrosis Development but Is not Indispensable for Fibrosis Development , 2014, Arthritis & rheumatology.

[36]  A. Parwani,et al.  Cartilage Oligomeric Matrix Protein in Idiopathic Pulmonary Fibrosis , 2013, PloS one.

[37]  A. Auerbach,et al.  Telomere Phenotypes in Females with Heterozygous Mutations in the Dyskeratosis Congenita 1 (DKC1) Gene , 2013, Human mutation.

[38]  Kelly J. Morris,et al.  A complex secretory program orchestrated by the inflammasome controls paracrine senescence , 2013, Nature Cell Biology.

[39]  David B. Darr,et al.  Monitoring Tumorigenesis and Senescence In Vivo with a p16 INK4a -Luciferase Model , 2013, Cell.

[40]  E. Blackburn,et al.  The telomere syndromes , 2012, Nature Reviews Genetics.

[41]  H. Chu,et al.  Cigarette smoke induces growth differentiation factor 15 production in human lung epithelial cells: Implication in mucin over-expression , 2012, Innate immunity.

[42]  W. Mitzner,et al.  Telomere length is a determinant of emphysema susceptibility. , 2011, American journal of respiratory and critical care medicine.

[43]  R. Tuder,et al.  Increased expression of growth differentiation factor-15 in systemic sclerosis-associated pulmonary arterial hypertension. , 2011, Chest.

[44]  S. Butz,et al.  GDF-15 is an inhibitor of leukocyte integrin activation required for survival after myocardial infarction in mice , 2011, Nature Medicine.

[45]  Takeshi Johkoh,et al.  American Thoracic Society Documents An Official ATS / ERS / JRS / ALAT Statement : Idiopathic Pulmonary Fibrosis : Evidence-based Guidelines for Diagnosis and Management , 2011 .

[46]  H. Grönberg,et al.  Macrophage inhibitory cytokine‐1 (MIC‐1/GDF15): a new marker of all‐cause mortality , 2010, Aging cell.

[47]  J. Campisi,et al.  The senescence-associated secretory phenotype: the dark side of tumor suppression. , 2010, Annual review of pathology.

[48]  M. Armanios Syndromes of telomere shortening. , 2009, Annual review of genomics and human genetics.

[49]  P. Lansdorp,et al.  Short telomeres are a risk factor for idiopathic pulmonary fibrosis , 2008, Proceedings of the National Academy of Sciences.

[50]  W. D. Fairlie,et al.  Tumor-induced anorexia and weight loss are mediated by the TGF-β superfamily cytokine MIC-1 , 2007, Nature Medicine.

[51]  J. Campisi,et al.  Cellular senescence: when bad things happen to good cells , 2007, Nature Reviews Molecular Cell Biology.

[52]  P. Lansdorp,et al.  Telomerase mutations in families with idiopathic pulmonary fibrosis. , 2007, The New England journal of medicine.

[53]  David Sidransky,et al.  A p53-type response element in the GDF15 promoter confers high specificity for p53 activation. , 2007, Biochemical and biophysical research communications.

[54]  T. Zimmers,et al.  GROWTH DIFFERENTIATION FACTOR-15/MACROPHAGE INHIBITORY CYTOKINE-1 INDUCTION AFTER KIDNEY AND LUNG INJURY , 2005, Shock.

[55]  N. Carter,et al.  A DNA damage checkpoint response in telomere-initiated senescence , 2003, Nature.

[56]  Paul J. Friedman,et al.  American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors , 2002, American journal of respiratory and critical care medicine.

[57]  S. Abid,et al.  Radiation-induced and chemotherapy-induced pulmonary injury , 2001, Current opinion in oncology.

[58]  J. Pilewski,et al.  Pharmacological modulation of ion transport across wild-type and DeltaF508 CFTR-expressing human bronchial epithelia. , 2000, American journal of physiology. Cell physiology.

[59]  L. Koniaris,et al.  Characterization of Growth-Differentiation Factor 15, a Transforming Growth Factor β Superfamily Member Induced following Liver Injury , 2000, Molecular and Cellular Biology.

[60]  David A. Lynch,et al.  Idiopathic pulmonary fibrosis: Diagnosis and treatment: International Consensus Statement , 2000 .

[61]  K. Unsicker,et al.  Characterization of the rat, mouse, and human genes of growth/differentiation factor-15/macrophage inhibiting cytokine-1 (GDF-15/MIC-1). , 1999, Gene.

[62]  C. Harley,et al.  Telomeres shorten during ageing of human fibroblasts , 1990, Nature.