Mdm2 ‐mediated ubiquitination of PKCβII is responsible for insulin‐induced heterologous desensitization of dopamine D3 receptor

In response to insulin stimulation, the E3 ligase enzyme Mdm2 exits the nucleus and interacts with PKC βII, facilitating the ubiquitination of PKCβII. Subsequently, the ubiquitinated PKCβII translocates to the cell membrane and associates with D3R, resulting in the inhibition of D3R cAMP signaling and linking it to clathrin-mediated endocytosis and degradation. The insulin and dopaminergic systems in the brain are associated with schizophrenia and Parkinson's disease with respect to etiology and treatment. The present study investigated the crosstalk between the insulin receptor (IR) and dopamine receptor and found that insulin stimulation selectively inhibits signaling of D3R in a PKC βII-dependent manner. Upon insulin stimulation, E3 ligase enzyme Mdm2 moves out of the nucleus to ubiquitinate PKCβII. Subsequently, ubiquitinated PKCβII translocates to the cell membrane and interacts with D3R in a phosphorylation-dependent manner at S229/257, resulting in the attenuation of D3R signaling and initiating clathrin-mediated endocytosis and downregulation. Considering that both IR and D3R are closely related to some neuropsychosis, this study could provide new molecular insight into the etiology of the disorder.
Source: FEBS Letters - Category: Biochemistry Authors: Tags: Research Article Source Type: research