Attenuated palmitoylation of serotonin receptor 5-HT1A affects receptor function and contributes to depression-like behaviors.
Nataliya GorinskiMonika BijataSonal PrasadAlexander WirthDalia Abdel GalilAndre ZeugDaria BazovkinaElena KondaurovaElizabeth KulikovaTatiana IlchibaevaMonika Zaręba-KoziołFrancesco PapaleoDiego ScheggiaGaga KochlamazashviliAlexander DityatevIan SmythAdam KrzystyniakJakub WlodarczykDiethelm W RichterTatyana StrekalovaStephan SigristClaudia BangLisa HobußJan FiedlerThomas ThumVladimir S NaumenkoGhanshyam PandeyEvgeni G PonimaskinPublished in: Nature communications (2019)
The serotonergic system and in particular serotonin 1A receptor (5-HT1AR) are implicated in major depressive disorder (MDD). Here we demonstrated that 5-HT1AR is palmitoylated in human and rodent brains, and identified ZDHHC21 as a major palmitoyl acyltransferase, whose depletion reduced palmitoylation and consequently signaling functions of 5-HT1AR. Two rodent models for depression-like behavior show reduced brain ZDHHC21 expression and attenuated 5-HT1AR palmitoylation. Moreover, selective knock-down of ZDHHC21 in the murine forebrain induced depression-like behavior. We also identified the microRNA miR-30e as a negative regulator of Zdhhc21 expression. Through analysis of the post-mortem brain samples in individuals with MDD that died by suicide we find that miR-30e expression is increased, while ZDHHC21 expression, as well as palmitoylation of 5-HT1AR, are reduced within the prefrontal cortex. Our study suggests that downregulation of 5-HT1AR palmitoylation is a mechanism involved in depression, making the restoration of 5-HT1AR palmitoylation a promising clinical strategy for the treatment of MDD.
Keyphrases
- major depressive disorder
- poor prognosis
- depressive symptoms
- bipolar disorder
- long non coding rna
- cell proliferation
- binding protein
- sleep quality
- prefrontal cortex
- endothelial cells
- long noncoding rna
- oxidative stress
- signaling pathway
- high glucose
- smoking cessation
- diabetic rats
- functional connectivity
- drug induced
- subarachnoid hemorrhage