Defective CFTR leads to aberrant β-catenin activation and kidney fibrosis
Abstract Cystic fibrosis transmembrane conductance regulator (CFTR), known as a cAMP-activated Cl− channel, is widely expressed at the apical membrane of epithelial cells in a wide variety of tissues. Of note, despite the abundant expression of CFTR in mammalian kidney, the role of CFTR in kidney di...
Saved in:
Main Authors: | Jie Ting Zhang, Yan Wang, Jun Jiang Chen, Xiao Hu Zhang, Jian Da Dong, Lai Ling Tsang, Xiao Ru Huang, Zhiming Cai, Hui Yao Lan, Xiao Hua Jiang, Hsiao Chang Chan |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2017
|
Subjects: | |
Online Access: | https://doaj.org/article/12e229d7fb814a3bb6c5e7916e428cd8 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Magnesium implantation or supplementation ameliorates bone disorder in CFTR-mutant mice through an ATF4-dependent Wnt/β-catenin signaling
by: Jiankun Xu, et al.
Published: (2022) -
Defective CFTR expression and function are detectable in blood monocytes: development of a new blood test for cystic fibrosis.
by: Claudio Sorio, et al.
Published: (2011) -
Integrin β3 Induction Promotes Tubular Cell Senescence and Kidney Fibrosis
by: Shen Li, et al.
Published: (2021) -
Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators
by: Iwona M. Pranke, et al.
Published: (2017) -
Apigenin-induced lysosomal degradation of β-catenin in Wnt/β-catenin signaling
by: Chung-Ming Lin, et al.
Published: (2017)