Ubiquitin-dependent down-regulation of the neurokinin-1 receptor

Graeme S. Cottrell, Benjamin Padilla, Stella Pikios, Dirk Roosterman, Martin Steinhoff, Daphne Gehringer, Eileen F. Grady, Nigel W. Bunnett

Research output: Contribution to journalArticle

Abstract

Transient stimulation with substance P (SP) induces endocytosis and recycling of the neurokinin-1 receptor (NK1R). The effects of sustained stimulation by high concentrations of SP on NK1R trafficking and Ca2+ signaling, as may occur during chronic inflammation and pain, are unknown. Chronic exposure to SP (100 nM, 3 h) completely desensitized Ca2+ signaling by wild-type NK1R (NK1Rwt). Resensitization occurred after 16 h, and cycloheximide prevented resensitization, implicating new receptor synthesis. Lysine ubiquitination of G-protein-coupled receptors is a signal for their trafficking and degradation. Lysine-deficient mutant receptors (NK1RΔ5K/R, C-terminal tail lysines; and NK1RΔ10K/R, all intracellular lysines) were expressed at the plasma membrane and were functional because they responded to SP by endocytosis and by mobilization of Ca2+ ions. SP desensitized NK1Rwt, NK1RΔ5K/R, and NK 1RΔ10K/R. However, NK1RΔ5K/R and NK 1RΔ10K/R resensitized 4-8-fold faster than NK1Rwt by cycloheximide-independent mechanisms. NK1RΔ325 (a naturally occurring truncated variant) showed incomplete desensitization, followed by a marked sensitization of signaling. Upon labeling receptors in living cells using antibodies to extracellular epitopes, we observed that SP induced endocytosis of NK1Rwt, NK1RΔ5K/R, and NK1RΔ10K/ R. After 4 h in SP-free medium, NK1RΔ5K/R and NK 1RΔ10K/R recycled to the plasma membrane, whereas NK 1Rwt remained internalized. SP induced ubiquitination of NK 1Rwt and NK1RΔ5K/R as determined by immunoprecipitation under nondenaturing and denaturing conditions and detected with antibodies for mono- and polyubiquitin. NK1RΔ10K/R was not ubiquitinated. Whereas SP induced degradation of NK1Rwt, NK 1RΔ5K/R and NK1RΔ10K/R showed ∼50% diminished degradation. Thus, chronic stimulation with SP induces ubiquitination of the NK1R, which mediates its degradation and down-regulation.

Original languageEnglish (US)
Pages (from-to)27773-27783
Number of pages11
JournalJournal of Biological Chemistry
Volume281
Issue number38
DOIs
StatePublished - Sep 22 2006

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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    Cottrell, G. S., Padilla, B., Pikios, S., Roosterman, D., Steinhoff, M., Gehringer, D., Grady, E. F., & Bunnett, N. W. (2006). Ubiquitin-dependent down-regulation of the neurokinin-1 receptor. Journal of Biological Chemistry, 281(38), 27773-27783. https://doi.org/10.1074/jbc.M603369200