Search Results

You are looking at 1 - 1 of 1 items for

  • Author: LA Noon x
  • Refine by access: All content x
Clear All Modify Search
LA Noon
Search for other papers by LA Noon in
Google Scholar
PubMed
Close
,
JM Franklin
Search for other papers by JM Franklin in
Google Scholar
PubMed
Close
,
PJ King
Search for other papers by PJ King in
Google Scholar
PubMed
Close
,
NJ Goulding
Search for other papers by NJ Goulding in
Google Scholar
PubMed
Close
,
L Hunyady
Search for other papers by L Hunyady in
Google Scholar
PubMed
Close
, and
AJ Clark
Search for other papers by AJ Clark in
Google Scholar
PubMed
Close

Difficulty in expressing the adrenocorticotrophin (ACTH) receptor (melanocortin 2 receptor; MC2R) after transfection of various MC2R expression vectors has been experienced by many researchers. Reproducible evidence for expression has been obtained only in the Y6/OS3 corticoadrenal cell lines or in cells expressing endogenous melanocortin receptors. In order to determine the cause of this failure of expression we have undertaken the following studies. An MC2R expression plasmid was constructed in which the green fluorescent protein (GFP) coding region had been added to the C-terminus of the mature protein. Transfection of this plasmid into Y6 cells with a cAMP-responsive reporter plasmid demonstrated normal function of this receptor. Imaging of CHO cells expressing MC2R-GFP revealed perinuclear expression, although a cholecystokinin receptor (CCKR)-GFP construct was efficiently expressed at the cell surface. Y6 cells, in contrast, showed cell surface fluorescence after transfection with MC2R-GFP. Several other cell types showed a similar pattern of GFP distribution characteristic of retention in the endoplasmic reticulum. Counterstaining with an anti-KDEL antibody confirmed this location. Co-expression of the MC2R and the CCKR-GFP did not impair CCKR trafficking to the cell surface, implying a receptor-specific impairment to trafficking in the CHO cell which was absent in the Y6 cell.

Free access