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10.1038/s41598-021-86037-0 http://scihub22266oqcxt.onion/10.1038/s41598-021-86037-0 33758289!7988136!33758289     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=33758289&cmd=llinks): Failed to open stream: HTTP request failed! 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Long-term evolution of the epithelial cell secretome in preclinical 3D models of the human bronchial epithelium |pdf=|usr=}}{{33758289}} gab.com Text Long-term evolution of the epithelial cell secretome in preclinical 3D models of the human bronchial epithelium JO: Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=33758289 #FOAvip The human bronchial epithelium is the first line of defense against atmospheric particles, pollutants, and respiratory pathogens such as the novel SARS-CoV-2. The epithelial cells form a tight barrier and secrete proteins that are major components of the mucosal immune response. Functional in vitro models of the human lung are essential for screening the epithelial response and assessing the toxicity and barrier crossing of drugs, inhaled particles, and pollutants. However, there is a lack of models to investigate the effect of chronic exposure without resorting to animal testing. Here, we developed a 3D model of the human bronchial epithelium using Calu-3 cell line and demonstrated its viability and functionality for 21 days without subculturing. We investigated the effect of reduced Fetal Bovine Serum supplementation in the basal medium and defined the minimal supplementation needed to maintain a functional epithelium, so that the amount of exogenous serum proteins could be reduced during drug testing. The long-term evolution of the epithelial cell secretome was fully characterized by quantitative mass spectrometry in two preclinical models using Calu-3 or primary NHBE cells. 408 common secreted proteins were identified while significant differences in protein abundance were observed with time, suggesting that 7-10 days are necessary to establish a mature secretome in the Calu-3 model. The associated Reactome pathways highlight the role of the secreted proteins in the immune response of the bronchial epithelium. We suggest this preclinical 3D model can be used to evaluate the long-term toxicity of drugs or particles on the human bronchial epithelium, and subsequently to investigate their effect on the epithelial cell secretions. Twit Text FOAVip Long-term evolution of the epithelial cell secretome in preclinical 3D models of the human bronchial epithelium ????Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=33758289 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33758289 #FOAvip English Wikipedia <ref>{{Cite pmid|33758289}}</ref> Long-term evolution of the epithelial cell secretome in preclinical 3D models of the human bronchial epithelium #MMPMID33758289 Sanchez-Guzman D; Boland S; Brookes O; Mc Cord C; Lai Kuen R; Sirri V; Baeza Squiban A; Devineau S Sci Rep 2021[Mar]; 11 (1): 6621 PMID33758289show ga The human bronchial epithelium is the first line of defense against atmospheric particles, pollutants, and respiratory pathogens such as the novel SARS-CoV-2. The epithelial cells form a tight barrier and secrete proteins that are major components of the mucosal immune response. Functional in vitro models of the human lung are essential for screening the epithelial response and assessing the toxicity and barrier crossing of drugs, inhaled particles, and pollutants. However, there is a lack of models to investigate the effect of chronic exposure without resorting to animal testing. Here, we developed a 3D model of the human bronchial epithelium using Calu-3 cell line and demonstrated its viability and functionality for 21 days without subculturing. We investigated the effect of reduced Fetal Bovine Serum supplementation in the basal medium and defined the minimal supplementation needed to maintain a functional epithelium, so that the amount of exogenous serum proteins could be reduced during drug testing. The long-term evolution of the epithelial cell secretome was fully characterized by quantitative mass spectrometry in two preclinical models using Calu-3 or primary NHBE cells. 408 common secreted proteins were identified while significant differences in protein abundance were observed with time, suggesting that 7-10 days are necessary to establish a mature secretome in the Calu-3 model. The associated Reactome pathways highlight the role of the secreted proteins in the immune response of the bronchial epithelium. We suggest this preclinical 3D model can be used to evaluate the long-term toxicity of drugs or particles on the human bronchial epithelium, and subsequently to investigate their effect on the epithelial cell secretions. |Angiotensin-Converting Enzyme 2/metabolism[MESH] |Bronchi/cytology[MESH] |COVID-19/pathology/virology[MESH] |Cell Culture Techniques[MESH] |Cell Line[MESH] |Culture Media/chemistry[MESH] |Epithelial Cells/cytology/*metabolism[MESH] |Humans[MESH] |Mass Spectrometry[MESH] |Models, Biological[MESH] |Principal Component Analysis[MESH] |Proteome/*analysis[MESH] |Proteomics/*methods[MESH]Long-term evolution of the epithelial cell secretome in preclinical 3D(epmc).pdf DeepDyve Pubget Overpricing