Niebert Sabine, van Belle Gijsbert J, Vogelgesang Steffen, Manzke Till, Niebert Marcus
Department of Maxillofacial Surgery, University Medical CenterGöttingen, Germany.
Institute of Cardiovascular Physiology, University Medical CenterGöttingen, Germany.
Front Mol Neurosci. 2017 Sep 21;10:299. doi: 10.3389/fnmol.2017.00299. eCollection 2017.
Previously, we described the dysregulation of serotonin (5-HT) receptor subtype 5b (5-ht) in a mouse model of Rett syndrome (RTT). 5-ht has not been extensively studied, so we set out to characterize it in more detail. Unlike common cell surface receptors, 5-ht displays no membrane expression, while receptor clusters are located in endosomes. This unusual subcellular localization is at least in part controlled by glycosylation of the N-terminus, with 5-ht possessing fewer glycosylation sites than related receptors. We analyzed whether the localization to endosomes has any functional relevance and found that 5-ht receptors can specifically interact with 5-HT receptors and retain them in endosomal compartments. This interaction reduces 5-HT surface expression and is mediated by interactions between the fourth and fifth trans-membrane domain (TMD). This possibly represents a mechanism by which 5-ht receptors regulate the activity of other 5-HT receptor.
此前,我们在雷特综合征(RTT)小鼠模型中描述了血清素(5-羟色胺,5-HT)受体亚型5b(5-ht)的失调。5-ht尚未得到广泛研究,因此我们着手更详细地对其进行表征。与常见的细胞表面受体不同,5-ht没有膜表达,而受体簇位于内体中。这种不寻常的亚细胞定位至少部分受N端糖基化控制,5-ht的糖基化位点比相关受体少。我们分析了定位于内体是否具有任何功能相关性,发现5-ht受体可以与5-HT受体特异性相互作用并将它们保留在内体区室中。这种相互作用降低了5-HT的表面表达,并由第四和第五跨膜结构域(TMD)之间的相互作用介导。这可能代表了5-ht受体调节其他5-HT受体活性的一种机制。