Intracellularly located misfolded glycoprotein hormone receptors associate with different chaperone proteins than their cognate wild-type receptors

Mol Endocrinol. 2004 Jul;18(7):1768-77. doi: 10.1210/me.2003-0406. Epub 2004 Apr 22.

Abstract

Most loss-of-function mutations of the glycoprotein hormone receptors have been found to be due to the misfolding of the receptor, resulting in its intracellular retention and, therefore, decreased cell surface expression. Chaperone proteins within the endoplasmic reticulum play an essential role in facilitating the folding of newly synthesized proteins and in recognizing and segregating misfolded proteins, thereby preventing their transit to the Golgi. The present study was conducted to begin to elucidate the role of chaperone proteins in the folding of the glycoprotein hormone receptors and misfolded mutants thereof. Toward this end, we examined the potential associations of calnexin, calreticulin, Grp94, BiP, ERp57, and protein disulfide-isomerase with each of the three glycoprotein hormone receptors. Calnexin, calreticulin, and protein disulfide-isomerase were found to associate with the immature forms of all three wild-type (wt) glycoprotein hormone receptors. As examples of misfolded glycoprotein hormone receptors, we studied two human LH receptor (hLHR) loss-of-function mutants that we show to be expressed predominantly as immature forms that are retained intracellularly. Significantly, the patterns of chaperone protein associations with the misfolded hLHR mutants differ from that observed with the wt hLHR. Furthermore, and unexpectedly, the chaperone protein associations were found to differ between the two misfolded hLHR mutants. Altogether, our studies show that although the same chaperone proteins are used by the three wt glycoprotein hormone receptors, different chaperone proteins associate with misfolded mutants thereof, and the specificity of interactions can vary between mutants, most likely reflecting the different stages of folding they achieve before being targeted for degradation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Calnexin / metabolism
  • Calreticulin / metabolism
  • Cells, Cultured
  • Endoplasmic Reticulum Chaperone BiP
  • HSP70 Heat-Shock Proteins / metabolism
  • Heat-Shock Proteins / metabolism
  • Humans
  • Isomerases / metabolism
  • Membrane Proteins / metabolism
  • Molecular Chaperones / chemistry
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism*
  • Mutation
  • Protein Disulfide-Isomerases / metabolism
  • Protein Folding
  • Receptors, FSH / chemistry
  • Receptors, FSH / metabolism*
  • Receptors, LH / chemistry
  • Receptors, LH / genetics
  • Receptors, LH / metabolism*
  • Receptors, Thyrotropin / chemistry
  • Receptors, Thyrotropin / metabolism*
  • Transfection

Substances

  • Calreticulin
  • Endoplasmic Reticulum Chaperone BiP
  • HSP70 Heat-Shock Proteins
  • Heat-Shock Proteins
  • Membrane Proteins
  • Molecular Chaperones
  • Receptors, FSH
  • Receptors, LH
  • Receptors, Thyrotropin
  • glucose-regulated proteins
  • Calnexin
  • Isomerases
  • Protein Disulfide-Isomerases
  • PDIA3 protein, human