Mucus aberrant properties in CF: Insights from cells and animal models.
Mucus aberrant properties in CF: Insights from cells and animal models.
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DOI:
10.1016/j.jcf.2022.08.019
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发表时间:
2023-03
影响因子:
5.2
通讯作者:
Ostedgaard, Lynda S.
中科院分区:
文献类型:
--
作者:
Ehre, Camille;Hansson, Gunnar C.;Thornton, David J.;Ostedgaard, Lynda S.
Cystic fibrosis (CF), an autosomal genetic disorder caused by the dysfunction of the cystic fibrosis transmembrane conductance regulator (CFTR) protein, is characterized by mucus accumulation in the lungs, the intestinal tract, and the pancreatic ducts. Mucins are high-molecular-weight glycoproteins that govern the biochemical and biophysical properties of mucus. In the CF lung, increased mucus viscoelasticity is associated with decreased mucociliary clearance and defects in host defense mechanisms. The link between defective ion channel and abnormal mucus properties has been investigated in studies involving cell and animal models. In this review article, we discuss recent progress toward understanding the different regions and cells that express CFTR in the airways and how mucus is produced and cleared from the lungs. In addition, we reflect on animal models that provided insights into the organization and the role of the mucin network and how mucus and antimicrobial activities act in concert to protect the lungs from invading pathogens.
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DOI:
10.1183/13993003.00457-2018
发表时间:
2018-08
期刊:
The European respiratory journal
影响因子:
--
作者:
Ermund A;Meiss LN;Dolan B;Bähr A;Klymiuk N;Hansson GC
通讯作者:
Hansson GC
DOI:
10.1183/13993003.00185-2021
发表时间:
2022-03
期刊:
The European respiratory journal
影响因子:
--
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通讯作者:
Ehre C
影响因子:
3.9
作者:
Dubaissi E
通讯作者:
Dubaissi E
DOI:
10.1126/science.1255825
发表时间:
2014-08-15
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Hoegger MJ;Fischer AJ;McMenimen JD;Ostedgaard LS;Tucker AJ;Awadalla MA;Moninger TO;Michalski AS;Hoffman EA;Zabner J;Stoltz DA;Welsh MJ
通讯作者:
Welsh MJ
影响因子:
8
作者:
Fischer, Anthony J.;Pino-Argumedo, Maria, I;Abou Alaiwa, Mahmoud H.
通讯作者:
Abou Alaiwa, Mahmoud H.