Mucus Hypersecretion and Ciliary Impairment in Conducting Airway Contribute to Alveolar Mucus Plugging in Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease attributed to the complex interplay of genetic and environmental risks. The muco-ciliary clearance (MCC) system plays a critical role in maintaining the conduit for air to and from the alveoli, but it remains poorly understood whether the...

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Detalles Bibliográficos
Autores principales: Peng, Yang, Wang, Zhao-Ni, Xu, Ai-Ru, Fang, Zhang-Fu, Chen, Shi-Ying, Hou, Xiao-Tao, Zhou, Zi-Qing, Lin, Hui-Min, Xie, Jia-Xing, Tang, Xiao Xiao, Wang, De-Yun, Zhong, Nan-Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842394/
https://www.ncbi.nlm.nih.gov/pubmed/35174169
http://dx.doi.org/10.3389/fcell.2021.810842

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842394/
https://www.ncbi.nlm.nih.gov/pubmed/35174169
http://dx.doi.org/10.3389/fcell.2021.810842

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