Abstract
Morphine is a poor inducer of μ-opioid receptor (MOR) internalization, but a potent inducer of cellular tolerance. Here we show that, in contrast to full agonists such as [D-Ala2-MePhe4-Gly-ol]enkephalin (DAMGO), morphine stimulated a selective phosphorylation of the carboxy-terminal residue 375 (Ser375). Ser375 phosphorylation was sufficient and required for morphine-induced desensitization of MOR. In the presence of full agonists, morphine revealed partial agonistic properties and potently inhibited MOR phosphorylation and internalization. Upon removal of the drug, DAMGO-desensitized receptors were rapidly dephosphorylated. In contrast, morphine-desensitized receptors remained at the plasma membrane in a Ser 375-phosphorylated state for prolonged periods. Thus, morphine promotes terminal MOR desensitization by inducing a persistent modification of Ser375.
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Schulz, S., Mayer, D., Pfeiffer, M., Stumm, R., Koch, T., & Höllt, V. (2004). Morphine induces terminal μ-opioid receptor desensitization by sustained phosphorylation of serine-375. EMBO Journal, 23(16), 3282–3289. https://doi.org/10.1038/sj.emboj.7600334
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