Cargando…

Modulator Combination Improves In Vitro the Microrheological Properties of the Airway Surface Liquid of Cystic Fibrosis Airway Epithelia

Cystic fibrosis (CF) is a genetic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) protein, a plasma membrane protein expressed on the apical surface of secretory epithelia of the airways. In the airways, defective or absent function of the CFTR protein d...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ludovico, Alessandra, Moran, Oscar, Baroni, Debora
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569604/ https://www.ncbi.nlm.nih.gov/pubmed/36232697 http://dx.doi.org/10.3390/ijms231911396

Ejemplares similares

Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia
por: Gianotti, Ambra, et al.
Publicado: (2020)

The Application of Bicarbonate Recovers the Chemical-Physical Properties of Airway Surface Liquid in Cystic Fibrosis Epithelia Models
por: Ferrera, Loretta, et al.
Publicado: (2021)

Soluble Mediators, Not Cilia, Determine Airway Surface Liquid Volume in Normal and Cystic Fibrosis Superficial Airway Epithelia
por: Tarran, Robert, et al.
Publicado: (2006)

Paracellular bicarbonate flux across human cystic fibrosis airway epithelia tempers changes in airway surface liquid pH
por: Thornell, Ian M., et al.
Publicado: (2020)

WNK Inhibition Increases Surface Liquid pH and Host Defense in Cystic Fibrosis Airway Epithelia
por: Rehman, Tayyab, et al.
Publicado: (2022)

Lipoxin A(4) Stimulates Calcium-Activated Chloride Currents and Increases Airway Surface Liquid Height in Normal and Cystic Fibrosis Airway Epithelia
por: Verrière, Valia, et al.
Publicado: (2012)

Polarized Signaling via Purinoceptors in Normal and Cystic Fibrosis Airway Epithelia
por: Paradiso, Anthony M., et al.
Publicado: (2001)

Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia
Publicado: (1992)

Klotho Inhibits Interleukin-8 Secretion from Cystic Fibrosis Airway Epithelia
por: Krick, Stefanie, et al.
Publicado: (2017)

Airway Surface Liquid and Impaired Antiviral Defense in Cystic Fibrosis
por: Voynow, Judith A., et al.
Publicado: (2020)

Airway Epithelia
por: Johnson, Larry G., et al.
Publicado: (2003)

Small molecule ion channels increase host defenses in cystic fibrosis airway epithelia
por: Muraglia, Katrina A., et al.
Publicado: (2019)

Thick airway surface liquid volume and weak mucin expression in pendrin-deficient human airway epithelia
por: Lee, Hyun Jae, et al.
Publicado: (2015)

Airway surface liquid pH is not acidic in children with cystic fibrosis
por: Schultz, André, et al.
Publicado: (2017)

Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis
por: Simonin, Juliette, et al.
Publicado: (2019)

Proteome of airway surface liquid and mucus in newborn wildtype and cystic fibrosis piglets
por: Rodriguez-Piñeiro, Ana M., et al.
Publicado: (2023)

Inflammation as a Regulator of the Airway Surface Liquid pH in Cystic Fibrosis
por: Rehman, Tayyab, et al.
Publicado: (2023)

Measuring Airway Surface Liquid Depth in Ex Vivo Mouse Airways by X-Ray Imaging for the Assessment of Cystic Fibrosis Airway Therapies
por: Morgan, Kaye S., et al.
Publicado: (2013)

Dynamic regulation of airway surface liquid pH by TMEM16A and SLC26A4 in cystic fibrosis nasal epithelia with rare mutations
por: Delpiano, Livia, et al.
Publicado: (2023)

Correction: Measuring Airway Surface Liquid Depth in Ex Vivo Mouse Airways by X-Ray Imaging for the Assessment of Cystic Fibrosis Airway Therapies
Publicado: (2014)

Hypercapnia modulates cAMP signalling and cystic fibrosis transmembrane conductance regulator‐dependent anion and fluid secretion in airway epithelia
por: Turner, Mark J., et al.
Publicado: (2015)

Cystic fibrosis swine fail to secrete airway surface liquid in response to inhalation of pathogens
por: Luan, Xiaojie, et al.
Publicado: (2017)

Pulmonary fibrosis distal airway epithelia are dynamically and structurally dysfunctional
por: Stancil, Ian T., et al.
Publicado: (2021)

Assisting PNA transport through cystic fibrosis human airway epithelia with biodegradable hybrid lipid-polymer nanoparticles
por: Comegna, Marika, et al.
Publicado: (2021)

The cystic fibrosis lower airways microbial metagenome
por: Moran Losada, Patricia, et al.
Publicado: (2016)

The Effect of CFTR Modulators on Airway Infection in Cystic Fibrosis
por: Harvey, Caitlyn, et al.
Publicado: (2022)

Esomeprazole Increases Airway Surface Liquid pH in Primary Cystic Fibrosis Epithelial Cells
por: Delpiano, Livia, et al.
Publicado: (2018)

Author Correction: Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis
por: Simonin, Juliette, et al.
Publicado: (2019)

In vitro Methods for the Development and Analysis of Human Primary Airway Epithelia
por: Gianotti, Ambra, et al.
Publicado: (2018)

The use of in vitro human airway epithelia for the development of novel antivirals
por: Huang, S., et al.
Publicado: (2016)

The Cystic Fibrosis Upper and Lower Airway Metagenome
por: Pienkowska, Katarzyna, et al.
Publicado: (2023)

Modulation of Ion Transport to Restore Airway Hydration in Cystic Fibrosis
por: Reihill, James A., et al.
Publicado: (2021)

Pendrin stimulates a chloride absorption pathway to increase CFTR‐mediated chloride secretion from Cystic Fibrosis airway epithelia
por: Bajko, Jeffrey, et al.
Publicado: (2020)

Microrheology
por: Frust, Eric M, et al.
Publicado: (2017)

The fungal airway microbiome in cystic fibrosis and non-cystic fibrosis bronchiectasis
por: Cuthbertson, Leah, et al.
Publicado: (2021)

Non-Genomic Estrogen Regulation of Ion Transport and Airway Surface Liquid Dynamics in Cystic Fibrosis Bronchial Epithelium
por: Saint-Criq, Vinciane, et al.
Publicado: (2013)

NBD2 Is Required for the Rescue of Mutant F508del CFTR by a Thiazole-Based Molecule: A Class II Corrector for the Multi-Drug Therapy of Cystic Fibrosis
por: Brandas, Chiara, et al.
Publicado: (2021)

Changes in the Cystic Fibrosis Airway Microbiome in Response to CFTR Modulator Therapy
por: Yi, Buqing, et al.
Publicado: (2021)

CFTR Modulator Therapies: Potential Impact on Airway Infections in Cystic Fibrosis
por: Saluzzo, Francesca, et al.
Publicado: (2022)

Pathogenesis of Achromobacter xylosoxidans respiratory infections: colonization and persistence of airway epithelia and differential gene expression in synthetic cystic fibrosis sputum medium
por: Billiot, Caitlin E., et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_c9f3ncf96vb9i24jf175kpcto3