CFTR dysfunction in smooth muscle drives TGFβ dependent airway hyperreactivity
Abstract Background The primary underlying defect in cystic fibrosis (CF) is disrupted ion transport in epithelia throughout the body. It is unclear if symptoms such as airway hyperreactivity (AHR) and increased airway smooth muscle (ASM) volume in people with CF are due to inherent abnormalities in...
Main Authors: | Elizabeth L. Kramer, Kristin M. Hudock, Cynthia R. Davidson, John P. Clancy |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2023-08-01
|
Series: | Respiratory Research |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12931-023-02495-2 |
Similar Items
-
The Effect of CFTR Modulators on Airway Infection in Cystic Fibrosis
by: Caitlyn Harvey, et al.
Published: (2022-03-01) -
CFTR dysfunction leads to defective bacterial eradication on cystic fibrosis airways
by: Min Wu, et al.
Published: (2024-04-01) -
The CFTR Amplifier Nesolicaftor Rescues TGF-β1 Inhibition of Modulator-Corrected F508del CFTR Function
by: Charles Bengtson, et al.
Published: (2022-09-01) -
Impact of Airway Inflammation on the Efficacy of CFTR Modulators
by: Carla M. P. Ribeiro, et al.
Published: (2021-11-01) -
CFTR Modulator Therapies: Potential Impact on Airway Infections in Cystic Fibrosis
by: Francesca Saluzzo, et al.
Published: (2022-04-01)