Constitutive and agonist-dependent self-association of the cell surface human lutropin receptor

Ya-Xiong Tao1, Nathan B Johnson, Deborah L Segaloff

  • 1Department of Physiology and Biophysics, University of Iowa, Iowa City, Iowa 52242, USA.

Insights

The human lutropin receptor (hLHR) self-associates in cells. This receptor dimerization and oligomerization depend on its cellular location, impacting reproductive physiology.

Area of Science:

  • Biochemistry
  • Cell Biology
  • Reproductive Endocrinology

Background:

  • The human lutropin receptor (hLHR) is a crucial G protein-coupled receptor (GPCR) in reproductive physiology.
  • Understanding hLHR's self-association is key to its function and regulation.

Purpose of the Study:

  • To investigate the self-association of the human lutropin receptor (hLHR).
  • To determine how cellular distribution affects hLHR dimerization and oligomerization.

Main Methods:

  • Co-immunoprecipitation of differentially tagged hLHRs in transfected 293 cells.
  • Analysis of hLHR complexes in transiently and stably transfected cells.
  • Assessment of hLHR association with wild-type and misfolded mutants.

Main Results:

  • hLHR self-associates in vivo, forming high molecular weight complexes.
  • In transiently transfected cells, immature hLHR predominantly self-associates in the ER.
  • In stably transfected cells, cell surface hLHR forms dimers/oligomers, increasing with human choriogonadotropin treatment.

Conclusions:

  • hLHR self-association occurs and is influenced by its cellular localization.
  • Misfolded mutants can disrupt wild-type hLHR trafficking and cell surface expression.
  • GPCR dimerization and oligomerization are critically dependent on cellular distribution.

Related Concept Videos

Receptor-mediated Endocytosis01:38

Receptor-mediated Endocytosis

Overview
Cell-surface Signaling01:21

Cell-surface Signaling

Hormones—or any molecule that binds to a receptor, known as a ligand—that are lipid-insoluble (water-soluble) are not able to diffuse across the cell membrane. In order to be able to affect a cell without entering it, these hormones bind to receptors on the cell membrane. When a first messenger, a hormone, binds to a receptor, a signal cascade is set off, causing second messengers, proteins inside the cell, to become activated, resulting in downstream effects.
Internal Receptors01:31

Internal Receptors

Many cellular signals are hydrophilic and therefore cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind to internal, or intracellular, receptors that reside within the cell. Many mammalian steroid hormones use this mechanism of cell signaling, as does nitric oxide (NO) gas.
Receptor-mediated Endocytosis01:20

Receptor-mediated Endocytosis

Receptor-mediated endocytosis is when bulk amounts of specific molecules are imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle.
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...
Types of Receptors: Cell Surface Receptors01:28

Types of Receptors: Cell Surface Receptors

Cell-surface receptors, also known as transmembrane receptors, are cell surface, membrane-anchored (integral) proteins that bind to external ligand molecules. This type of receptor spans the plasma membrane and performs signal transduction, converting an extracellular signal into an intracellular signal. Ligands that interact with cell-surface receptors do not have to enter the cell that they affect. Cell-surface receptors are also called cell-specific proteins or markers because they are...
The Two-State Receptor Model01:29

The Two-State Receptor Model

The two-state receptor model explains a drug's interaction with receptors, such as G protein-coupled receptors and ligand-gated ion channels, to induce or inhibit a biological response. When no natural ligands are present, a receptor exists in an equilibrium of inactive (Ri) and active (Ra) conformations. The inactive form does not produce a response, while the active form generates a basal effect known as constitutive activity.
The binding affinity of a drug determines its interaction with one...