Gap Junctions Are Involved in the Rescue of CFTR-Dependent Chloride Efflux by Amniotic Mesenchymal Stem Cells in Coculture with Cystic Fibrosis CFBE41o- Cells
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A. Angiolillo | M. Conese | S. Di Gioia | M. Seia | M. Favia | A. Carbone | C. Colombo | Elisa Beccia | V. Casavola | S. Castellani | R. Zefferino | Valentina Giannone
[1] P. Zoppoli,et al. Human monocyte-derived dendritic cells exposed to hyperthermia show a distinct gene expression profile and selective upregulation of IGFBP6 , 2017, Oncotarget.
[2] M. Yen,et al. Human mesenchymal stem cells (MSCs) for treatment towards immune- and inflammation-mediated diseases: review of current clinical trials , 2016, Journal of Biomedical Science.
[3] D. Chambers,et al. Characterization of intercellular communication and mitochondrial donation by mesenchymal stromal cells derived from the human lung , 2016, Stem Cell Research & Therapy.
[4] S. Sagel,et al. Cystic fibrosis: a model system for precision medicine , 2016, Current opinion in pediatrics.
[5] K. Akram,et al. Lung Regeneration: Endogenous and Exogenous Stem Cell Mediated Therapeutic Approaches , 2016, International journal of molecular sciences.
[6] N. McCarty,et al. Junctional abnormalities in human airway epithelial cells expressing F508del CFTR. , 2015, American journal of physiology. Lung cellular and molecular physiology.
[7] G. Giammona,et al. Cationic polyaspartamide-based nanocomplexes mediate siRNA entry and down-regulation of the pro-inflammatory mediator high mobility group box 1 in airway epithelial cells. , 2015, International journal of pharmaceutics.
[8] S. Mattoli,et al. Stem Cell-Based Therapy in Idiopathic Pulmonary Fibrosis , 2015, Stem Cell Reviews and Reports.
[9] D. Prockop,et al. An official American Thoracic Society workshop report: stem cells and cell therapies in lung biology and diseases. , 2015, Annals of the American Thoracic Society.
[10] D. Meyerholz,et al. Origins of cystic fibrosis lung disease. , 2015, The New England journal of medicine.
[11] Mandy B. Esch,et al. TEER Measurement Techniques for In Vitro Barrier Model Systems , 2015, Journal of laboratory automation.
[12] J. Whitsett,et al. Respiratory epithelial cells orchestrate pulmonary innate immunity , 2014, Nature Immunology.
[13] M. Conese,et al. Human amnion-derived cells: prospects for the treatment of lung diseases. , 2014, Current stem cell research & therapy.
[14] M. Conese,et al. Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells , 2014, Journal of cellular and molecular medicine.
[15] P. Lampe,et al. Specific Cx43 phosphorylation events regulate gap junction turnover in vivo , 2014, FEBS letters.
[16] M. Chanson,et al. Connexins in respiratory and gastrointestinal mucosal immunity , 2014, FEBS letters.
[17] M. Bacchetta,et al. Pseudomonas aeruginosa–Induced Apoptosis in Airway Epithelial Cells Is Mediated by Gap Junctional Communication in a JNK-Dependent Manner , 2014, The Journal of Immunology.
[18] J. Palmer,et al. Bitter and sweet taste receptors regulate human upper respiratory innate immunity. , 2014, The Journal of clinical investigation.
[19] Ashley M. Jacobi,et al. Post-transcriptional regulation of cystic fibrosis transmembrane conductance regulator expression and function by microRNAs. , 2013, American journal of respiratory cell and molecular biology.
[20] A. Caplan,et al. MSCs: Delivery Routes and Engraftment, Cell-Targeting Strategies, and Immune Modulation , 2013, Stem cells international.
[21] M. Conese,et al. Paracrine Effects and Heterogeneity of Marrow-Derived Stem/Progenitor Cells: Relevance for the Treatment of Respiratory Diseases , 2013, Cells Tissues Organs.
[22] I. Oglesby,et al. Regulation of Cystic Fibrosis Transmembrane Conductance Regulator by MicroRNA-145, -223, and -494 Is Altered in ΔF508 Cystic Fibrosis Airway Epithelium , 2013, The Journal of Immunology.
[23] M. Conese,et al. NHERF1 and CFTR restore tight junction organisation and function in cystic fibrosis airway epithelial cells: role of ezrin and the RhoA/ROCK pathway , 2012, Laboratory Investigation.
[24] Ashley M. Jacobi,et al. A microRNA network regulates expression and biosynthesis of wild-type and ΔF508 mutant cystic fibrosis transmembrane conductance regulator , 2012, Proceedings of the National Academy of Sciences.
[25] D. Rowlands,et al. Mitochondrial transfer from bone-marrow–derived stromal cells to pulmonary alveoli protects against acute lung injury , 2012, Nature Medicine.
[26] J. Laffey,et al. Acute lung injury/acute respiratory distress syndrome-a therapeutic challenge , 2012 .
[27] C. Piccoli,et al. Subcytotoxic mercury chloride inhibits gap junction intercellular communication by a redox- and phosphorylation-mediated mechanism. , 2012, Free radical biology & medicine.
[28] M. Zaccolo,et al. CFTR regulation in human airway epithelial cells requires integrity of the actin cytoskeleton and compartmentalized cAMP and PKA activity , 2012, Journal of Cell Science.
[29] Austin E. Gillen,et al. MicroRNA regulation of expression of the cystic fibrosis transmembrane conductance regulator gene. , 2011, The Biochemical journal.
[30] J. Clancy,et al. Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation , 2011, Thorax.
[31] M. Chanson,et al. Connexins as therapeutic targets in lung disease , 2011, Expert opinion on therapeutic targets.
[32] E. Kerem,et al. Managing cystic fibrosis: strategies that increase life expectancy and improve quality of life. , 2011, American journal of respiratory and critical care medicine.
[33] D. Pinsky,et al. Epithelial Interactions And Local Engraftment Of Lung-Resident Mesenchymal Stem Cells , 2011, ATS 2011.
[34] G. Roomans. Tissue engineering and the use of stem/progenitor cells for airway epithelium repair. , 2010, European cells & materials.
[35] D. Gruenert,et al. Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers , 2010, The Journal of physiology.
[36] M. Conese,et al. Na+/H+ Exchanger Regulatory Factor 1 Overexpression-dependent Increase of Cytoskeleton Organization Is Fundamental in the Rescue of F508del Cystic Fibrosis Transmembrane Conductance Regulator in Human Airway CFBE41o- Cells , 2010, Molecular biology of the cell.
[37] Francis J. Martin,et al. TLR2 Regulates Gap Junction Intercellular Communication in Airway Cells1 , 2008, The Journal of Immunology.
[38] M. Chanson,et al. Interactions of connexins with other membrane channels and transporters. , 2007, Progress in biophysics and molecular biology.
[39] R. Robbins,et al. Stem cell transplantation: the lung barrier. , 2007, Transplantation proceedings.
[40] R. Boucher,et al. Evidence for airway surface dehydration as the initiating event in CF airway disease , 2007, Journal of internal medicine.
[41] W. Guggino,et al. New insights into cystic fibrosis: molecular switches that regulate CFTR , 2006 .
[42] E. Bruscia,et al. Assessment of cystic fibrosis transmembrane conductance regulator (CFTR) activity in CFTR-null mice after bone marrow transplantation. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[43] R. Loi,et al. Limited restoration of cystic fibrosis lung epithelium in vivo with adult bone marrow-derived cells. , 2006, American journal of respiratory and critical care medicine.
[44] M. Conese,et al. Na+/H+ Exchanger Regulatory Factor Isoform 1 Overexpression Modulates Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Expression and Activity in Human Airway 16HBE14o- Cells and Rescues ΔF508 CFTR Functional Expression in Cystic Fibrosis Cells* , 2005, Journal of Biological Chemistry.
[45] D. Prockop,et al. Adult stem cells from bone marrow stroma differentiate into airway epithelial cells: potential therapy for cystic fibrosis. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[46] T. Tuschl,et al. Mechanisms of gene silencing by double-stranded RNA , 2004, Nature.
[47] J. Cassiman,et al. Established cell lines used in cystic fibrosis research. , 2004, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[48] Michael R Rosen,et al. Human mesenchymal stem cells make cardiac connexins and form functional gap junctions , 2004, The Journal of physiology.
[49] Robert A. Kloner,et al. Systemic Delivery of Bone Marrow–Derived Mesenchymal Stem Cells to the Infarcted Myocardium: Feasibility, Cell Migration, and Body Distribution , 2003, Circulation.
[50] Milan Macek,et al. Cystic fibrosis: A worldwide analysis of CFTR mutations—correlation with incidence data and application to screening , 2002, Human mutation.
[51] Carsten Kneuer,et al. Influence of apical fluid volume on the development of functional intercellular junctions in the human epithelial cell line 16HBE14o–: implications for the use of this cell line as an in vitro model for bronchial drug absorption studies , 2002, Cell and Tissue Research.
[52] R. Savani,et al. Heterocellular gap junctional communication between alveolar epithelial cells. , 2001, American journal of physiology. Lung cellular and molecular physiology.
[53] L. Dwyer-Nield,et al. Defective gap junctional intercellular communication in lung cancer: loss of an important mediator of tissue homeostasis and phenotypic regulation. , 2001, Experimental lung research.
[54] S. Boitano,et al. Connexin mimetic peptides reversibly inhibit Ca(2+) signaling through gap junctions in airway cells. , 2000, American journal of physiology. Lung cellular and molecular physiology.
[55] H. Dua. Amniotic membrane transplantation , 1999, The British journal of ophthalmology.
[56] D. Goodenough,et al. Diverse functions of vertebrate gap junctions. , 1998, Trends in cell biology.
[57] R. Schreiber,et al. The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways. , 1998, The Journal of clinical investigation.
[58] Satoshi Omura,et al. Degradation of CFTR by the ubiquitin-proteasome pathway , 1995, Cell.
[59] B. Huppertz,et al. Soluble factors of amnion-derived cells in treatment of inflammatory and fibrotic pathologies. , 2013, Current stem cell research & therapy.
[60] M. Bacchetta,et al. Prostaglandin E₂regulation of cystic fibrosis transmembrane conductance regulator activity and airway surface liquid volume requires gap junctional communication. , 2011, American journal of respiratory cell and molecular biology.
[61] S. Strom,et al. Amnion-derived pluripotent/multipotent stem cells , 2006, Stem Cell Reviews.