Acid Sphingomyelinase Inhibition Attenuates Cell Death in Mechanically Ventilated Newborn Rat Lung

التفاصيل البيبلوغرافية
العنوان: Acid Sphingomyelinase Inhibition Attenuates Cell Death in Mechanically Ventilated Newborn Rat Lung
المؤلفون: Leonardo Ermini, Behzad Yeganeh, Joyce S. Lee, Cameron Ackerley, Claudia Bilodeau, Jeroen Tibboel, Andre A. Kroon, Isabella Caniggia, Irene Lok, Martin Post
المساهمون: Pediatrics
المصدر: American Journal of Respiratory and Critical Care Medicine
American Journal of Respiratory and Critical Care Medicine, 199(6), 760-772. American Thoracic Society
سنة النشر: 2019
مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Programmed cell death, Pathology, medicine.medical_specialty, medicine.medical_treatment, Apoptosis, Sphingomyelin phosphodiesterase, Lung injury, Ceramides, Critical Care and Intensive Care Medicine, 03 medical and health sciences, Mechanical ventilation, 0302 clinical medicine, Models, Autophagy, medicine, Lung epithelial cells, Animals, Animals, Newborn, Cell Death, Epithelial Cells, Humans, Infant, Newborn, Lung, Models, Animal, Rats, Sphingomyelin Phosphodiesterase, Respiration, Artificial, 030212 general & internal medicine, Animal, business.industry, Respiration, Editorials, Infant, respiratory system, Newborn, medicine.disease, medicine.anatomical_structure, 030228 respiratory system, Bronchopulmonary dysplasia, Artificial, Acid sphingomyelinase, business, medicine.drug
الوصف: Premature infants subjected to mechanical ventilation (MV) are prone to lung injury that may result in bronchopulmonary dysplasia. MV causes epithelial cell death and halts alveolar development. The exact mechanism of MV-induced epithelial cell death is unknown.To determine the contribution of autophagy to MV-induced epithelial cell death in newborn rat lungs.Newborn rat lungs and fetal rat lung epithelial (FRLE) cells were exposed to MV and cyclic stretch, respectively, and were then analyzed by immunoblotting and mass spectrometry for autophagy, apoptosis, and bioactive sphingolipids.Both MV and stretch first induce autophagy (ATG 5-12 [autophagy related 5-12] and LC3B-II [microtubule-associated proteins 1A/1B light chain 3B-II] formation) followed by extrinsic apoptosis (cleaved CASP8/3 [caspase-8/3] and PARP [poly(ADP-ribose) polymerase] formation). Stretch-induced apoptosis was attenuated by inhibiting autophagy. Coimmunoprecipitation revealed that stretch promoted an interaction between LC3B and the FAS (first apoptosis signal) cell death receptor in FRLE cells. Ceramide levels, in particular C16 ceramide, were rapidly elevated in response to ventilation and stretch, and C16 ceramide treatment of FRLE cells induced autophagy and apoptosis in a temporal pattern similar to that seen with MV and stretch. SMPD1 (sphingomyelin phosphodiesterase 1) was activated by ventilation and stretch, and its inhibition prevented ceramide production, LC3B-II formation, LC3B/first apoptosis signal interaction, caspase-3 activation, and, ultimately, FLRE cell death. SMPD1 inhibition also attenuated ventilation-induced autophagy and apoptosis in newborn rats.Ventilation-induced ceramides promote autophagy-mediated cell death, and identifies SMPD1 as a potential therapeutic target for the treatment of ventilation-induced lung injury in newborns.
تدمد: 1073-449X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e518e5911041850a97b22288d3ea4e0Test
https://doi.org/10.1164/rccm.201803-0583ocTest
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....3e518e5911041850a97b22288d3ea4e0
قاعدة البيانات: OpenAIRE