Interactions between CFTR and other ion channels (WP1485)
Rattus norvegicus
The CFTR receptor (an ion channel, which transports CL- out of the cell) can form a complex with CFTR assiciated protein (CAL), followed by degradation. If NHERF1 is present it will form a complex with the CFTR receptor (by binding the PDZ1 region), inhibiting degradation. This complex will bind to other proteins / ion channels. One of these ion channels is the Slc26 family, which binds to the PDZ2 region of NHERF1. After forming this complex Cl- and NaHCO3 secretion will be performed. The same thing happens with the ENaC (an ion channel, which transports Na+), which consists of 3 subunits (alfa, beta & gamma). This channels binds YES-accosiated protein (YAP), which in his turn binds the PDZ2 region of NHERF1. Also c-YES will bind to NHERF1, which inhibits the ENaC channel. By forming this complex Cl- secretion will be induced, while Na+ absorption will be reduced.
Authors
Flipke , Thomas Kelder , Kristina Hanspers , Daniela Digles , Egon Willighagen , and Martina Summer-KutmonActivity
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Organisms
Rattus norvegicusCommunities
Annotations
Pathway Ontology
chloride ion transport pathwayLabel | Type | Compact URI | Comment |
---|---|---|---|
Cftr | GeneProduct | ensembl:ENSRNOG00000055103 | |
YAP | GeneProduct | ensembl:ENSRNOG00000005933 | |
ENaCa | GeneProduct | ensembl:ENSRNOG00000019368; | |
ENaCb | GeneProduct | ensembl:ENSRNOG00000030981 | |
NHERF1 | GeneProduct | ensembl:ENSRNOG00000003232 | |
CAL | GeneProduct | ensembl:ENSRNOG0000000408 | |
ENaCg | GeneProduct | ensembl:ENSRNOG00000017842 | |
c-Yes | GeneProduct | ncbigene:292256 |
References
- New insights into cystic fibrosis: molecular switches that regulate CFTR. Guggino WB, Stanton BA. Nat Rev Mol Cell Biol. 2006 Jun;7(6):426–36. PubMed Europe PMC Scholia