TY - JOUR T1 - Telomere shortening and DNA damage in culprit cells of different types of progressive fibrosing interstitial lung disease JF - ERJ Open Research JO - erjor DO - 10.1183/23120541.00691-2020 VL - 7 IS - 2 SP - 00691-2020 AU - Aernoud A. van Batenburg AU - Karin M. Kazemier AU - Matthijs F.M. van Oosterhout AU - Joanne J. van der Vis AU - Jan C. Grutters AU - Roel Goldschmeding AU - Coline H.M. van Moorsel Y1 - 2021/04/01 UR - http://openres.ersjournals.com/content/7/2/00691-2020.abstract N2 - Pulmonary fibrosis is strongly associated with telomere shortening and increased DNA damage. Key cells in the pathogenesis involve alveolar type 2 (AT2) cells, club cells and myofibroblasts; however, to what extent these cells are affected by telomere shortening and DNA damage is not yet known. We sought to determine the degree of, and correlation between, telomere shortening and DNA damage in different cell types involved in the pathogenesis of progressive fibrosing interstitial lung disease. Telomere length and DNA damage were quantified, using combined fluorescence in situ hybridisation and immunofluorescence staining techniques, in AT2 cells, club cells and myofibroblasts of controls and patients with pulmonary fibrosis and a telomerase reverse transcriptase mutation (TERT-PF), idiopathic pulmonary fibrosis (IPF) and fibrotic hypersensitivity pneumonitis (fHP). In IPF and TERT-PF lungs, AT2 cells contained shorter telomeres and expressed higher DNA damage signals than club cells and myofibroblasts. In fHP lungs, club cells contained highly elevated levels of DNA damage, while telomeres were not obviously short. In vitro, we found significantly shorter telomeres and higher DNA damage levels only in AT2 surrogate cell lines treated with telomerase inhibitor BIBR1532. Our study demonstrated that in IPF and TERT-PF lungs, telomere shortening and accumulation of DNA damage primarily affects AT2 cells, further supporting the importance of AT2 cells in these diseases, while in fHP the particularly high telomere-independent DNA damage signals in club cells underscores its bronchiolocentric pathogenesis. These findings suggest that cell type-specific telomere shortening and DNA damage may help to discriminate between different drivers of fibrogenesis.In patients with IPF, telomere shortening and accumulation of DNA damage primarily affects AT2 cells, while in fHP, the particularly high telomere-independent DNA damage signals in club cells underscore its bronchiolocentric pathogenesis https://bit.ly/35mP1JI ER -