Regulatory Crosstalk by Protein Kinases on CFTR Trafficking and Activity

被引:28
作者
Farinha, Carlos M. [1 ]
Swiatecka-Urban, Agnieszka [2 ,3 ]
Brautigan, David L. [4 ,5 ]
Jordan, Peter [1 ,6 ]
机构
[1] Univ Lisbon, Fac Sci, Biosyst & Integrat Sci Inst, Lisbon, Portugal
[2] Univ Pittsburgh, Sch Med, Dept Cell Biol, Pittsburgh, PA USA
[3] Univ Pittsburgh, Childrens Hosp Pittsburgh, Sch Med, UPMC, Pittsburgh, PA USA
[4] Univ Virginia, Sch Med, Ctr Cell Signaling, Charlottesville, VA 22908 USA
[5] Univ Virginia, Sch Med, Dept Microbiol Immunol & Canc Biol, Charlottesville, VA 22908 USA
[6] Natl Hlth Inst Dr Ricardo Jorge, Dept Human Genet, Lisbon, Portugal
关键词
CFTR; cystic fibrosis; phosphorylation; kinase; protein trafficking; TRANSMEMBRANE CONDUCTANCE REGULATOR; SYK TYROSINE KINASE; WNK KINASES; SURFACE EXPRESSION; MYOSIN-VI; ANTAGONISTIC REGULATION; MUTANT CFTR; CL-CHANNEL; HALF-LIFE; IN-VITRO;
D O I
10.3389/fchem.2016.00001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) is a member of the ATP binding cassette (ABC) transporter superfamily that functions as a cAMP-activated chloride ion channel in fluid-transporting epithelia. There is abundant evidence that CFTR activity (i.e., channel opening and closing) is regulated by protein kinases and phosphatases via phosphorylation and dephosphorylation. Here, we review recent evidence for the role of protein kinases in regulation of CFTR delivery to and retention in the plasma membrane. We review this information in a broader context of regulation of other transporters by protein kinases because the overall functional output of transporters involves the integrated control of both their number at the plasma membrane and their specific activity. While many details of the regulation of intracellular distribution of CFTR and other transporters remain to be elucidated, we hope that this review will motivate research providing new insights into how protein kinases control membrane transport to impact health and disease.
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页数:11
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