Pernecker Moritz, Dibos Miriam, Götz Sophie, Al-Monajjed Rouvier, Barz Vivien, Albiker Christian, Schröter Rita, Neugebauer Ute, Ludwig-Radtke Lena, Taudte R Verena, Vogl Thomas, Ciarimboli Giuliano
Exp. Nephrology, Med. Clinic D, University Hospital Münster, Albert-Schweitzer-Campus 1/A14, 48149, Münster, Germany.
Core Facility for Metabolomics, Department of Medicine, Philipps University Marburg, Marburg, Germany.
J Biomed Sci. 2025 Jul 12;32(1):68. doi: 10.1186/s12929-025-01158-2.
The organic cation transporter 3 (OCT3) is a ubiquitous transporter that carries both endogenous and exogenous substrates, such as histamine and cisplatin. Our investigations have shown that OCT3 directly interacts with the tetraspanin CD63. CD63 is a marker for activated basophils and mast cells, which are granulocytes capable of rapidly releasing large amounts of histamine. This makes them key players in the development of allergic reactions.
In this work, we demonstrated that OCT3 is present in murine and human basophils and is strongly colocalized with CD63 in a specific region of the plasma membrane, particularly after cell activation leading to histamine release. Furthermore, we confirmed that part of the histamine release from basophils is mediated by OCT3. In a mouse model of contact dermatitis, the presence of OCT3 is crucial for determining the severity of the allergic reaction. The presence of CD63 also seems to be important for regulating the allergic response, although it does not directly affect histamine secretion. RNA-Seq and metabolome analyses revealed that wild-type mice and mice with genetic deletion of OCT3 (OCT3) are phenotypically very similar, and that the observed effects in OCT3 organisms can be attributed mainly to the genetic deletion of the OCT3 transporter.
In conclusion, OCT3 is a transporter for histamine in granulocytes, which plays a crucial role in determining the intensity of allergic reactions and may be a target for interventions aimed at reducing their severity.
有机阳离子转运体3(OCT3)是一种普遍存在的转运体,可运载内源性和外源性底物,如组胺和顺铂。我们的研究表明,OCT3与四跨膜蛋白CD63直接相互作用。CD63是活化嗜碱性粒细胞和肥大细胞的标志物,这些粒细胞能够迅速释放大量组胺。这使它们成为过敏反应发展中的关键参与者。
在这项研究中,我们证明OCT3存在于小鼠和人类嗜碱性粒细胞中,并且在细胞膜的特定区域与CD63强烈共定位,特别是在导致组胺释放的细胞活化后。此外,我们证实嗜碱性粒细胞释放的部分组胺是由OCT3介导的。在接触性皮炎小鼠模型中,OCT3的存在对于确定过敏反应的严重程度至关重要。CD63的存在似乎对调节过敏反应也很重要,尽管它不直接影响组胺分泌。RNA测序和代谢组分析表明,野生型小鼠和OCT3基因缺失小鼠(OCT3 -/-)在表型上非常相似,并且在OCT3 -/-小鼠中观察到的效应主要可归因于OCT3转运体的基因缺失。
总之,OCT3是粒细胞中组胺的转运体,在确定过敏反应强度方面起关键作用,可能是旨在减轻其严重程度的干预靶点。