Thapsigargin or curcumin does not promote maturation of processing mutants of the ABC transporters, CFTR, and P-glycoprotein
TW Loo, MC Bartlett, DM Clarke - Biochemical and biophysical research …, 2004 - Elsevier
TW Loo, MC Bartlett, DM Clarke
Biochemical and biophysical research communications, 2004•ElsevierMisprocessed plasma membrane proteins of CFTR and P-glycoprotein (P-gp) are retained
in the endoplasmic reticulum (ER) by molecular chaperones. Depletion of the calcium stores
in the ER by the SERCA calcium pump inhibitors thapsigargin or curcumin inhibits these
interactions and allows the protein to be trafficked to the plasma membrane [Nat. Med. 8
(2002) 485; Science 304 (2004) 600]. We tested this hypothesis by treating various cell lines
expressing misprocessed mutants of CFTR or P-gp with thapsigargin or curcumin …
in the endoplasmic reticulum (ER) by molecular chaperones. Depletion of the calcium stores
in the ER by the SERCA calcium pump inhibitors thapsigargin or curcumin inhibits these
interactions and allows the protein to be trafficked to the plasma membrane [Nat. Med. 8
(2002) 485; Science 304 (2004) 600]. We tested this hypothesis by treating various cell lines
expressing misprocessed mutants of CFTR or P-gp with thapsigargin or curcumin …
Misprocessed plasma membrane proteins of CFTR and P-glycoprotein (P-gp) are retained in the endoplasmic reticulum (ER) by molecular chaperones. Depletion of the calcium stores in the ER by the SERCA calcium pump inhibitors thapsigargin or curcumin inhibits these interactions and allows the protein to be trafficked to the plasma membrane [Nat. Med. 8 (2002) 485; Science 304 (2004) 600]. We tested this hypothesis by treating various cell lines expressing misprocessed mutants of CFTR or P-gp with thapsigargin or curcumin. Conversion of the immature core-glycosylated protein to mature product was detected by immunoblot analysis of whole cell extracts. Mature product was not detected in any of the misprocessed mutants. By contrast, all misprocessed P-gp mutants were rescued by the chemical chaperone/drug substrate cyclosporin A in a dose-dependent manner. These results show that thapsigargin or curcumin is not effective in rescuing misprocessed mutants of P-gp and CFTR.
Elsevier