Deciphering the role of protein kinase CK2 in the maturation/stability of F508del-CFTR

https://doi.org/10.1016/j.bbadis.2019.165611Get rights and content
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Highlights

  • CFBE cells display an increased CK2 expression/activity than 16-HBE.

  • CK2 expression/activity is not impaired in primary bronchial cells from CF patients.

  • Abrogation of the CK2 catalytic subunits do not induce CFTR rescue in CFBE cells.

  • CK2α′ depletion hampers the efficacy of VX-809 on F508del-CFTR correction.

Abstract

F508del-CFTR, the most common mutation in cystic fibrosis (CF) patients, impairs CFTR trafficking to plasma membrane leading to its premature proteasomal degradation. Several post-translational modifications have been identified on CFTR with multiple roles in stability, localization and channel function, and the possibility to control the enzymes responsible of these modifications has been long considered a potential therapeutic strategy. Protein kinase CK2 has been previously suggested as an important player in regulating CFTR functions and it has been proposed as a pharmacological target in a combinatory therapy to treat CF patients. However, the real implication of CK2 in F508del-CFTR proteostasis, and in particular the hypothesis that its inhibition could be important in CF therapies, is still elusive. Here, by using immortalized cell lines, primary human cells, and knockout cell lines deprived of CK2 subunits, we do not disclose any direct correlation between F508del-CFTR proteostasis and CK2 expression/activity. Rather, our data indicate that the CK2α′ catalytic subunit should be preserved rather than inhibited for F508del rescue by the correctors of class-1, such as VX-809, disclosing new important features in CF therapeutic approaches.

Keywords

CK2
Cystic fibrosis
VX-809
F508del-CFTR correction

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