Shiers Stephanie, Sahn James J, Price Theodore J
Center for Advanced Pain Studies, School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, Texas, USA.
4E Therapeutics, Austin, Texas, USA.
bioRxiv. 2023 Jan 4:2023.01.04.522773. doi: 10.1101/2023.01.04.522773.
Mitogen activated protein kinase interacting kinases (MNK) 1 and 2 are serine/threonine protein kinases that play an important role in translation of mRNAs through their phosphorylation of the RNA 5’-cap binding protein, eukaryotic translation initiation factor (eIF) 4E. These kinases are downstream targets for mitogen activated protein kinases (MAPKs), extracellular activity regulated protein kinase (ERK) and p38. MNKs have been implicated in the sensitization of peripheral nociceptors of the dorsal root and trigeminal ganglion (DRG and TG) using transgenic mouse lines and through the use of specific inhibitors of MNK1 and MNK2. While specific knockout of the gene suggests that it is the key isoform for regulation of nociceptor excitability and nociceptive behaviors in mice, both and genes are expressed in the DRG and TG of mice and humans based on RNA sequencing experiments. Single cell sequencing in mice suggests that and may be expressed in different populations of nociceptors. We sought to characterize mRNA expression in human DRG and TG for both MNK1 and MNK2. Our results show that both genes are expressed by nearly all neurons in both human ganglia with expression in other cell types as well. Our findings provide evidence that MNK1 and MNK2 are expressed by human nociceptors and suggest that efforts to pharmacologically target MNKs for pain would likely be translatable due its conserved expression in both species.
丝裂原活化蛋白激酶相互作用激酶(MNK)1和2是丝氨酸/苏氨酸蛋白激酶,它们通过磷酸化RNA 5'-帽结合蛋白——真核翻译起始因子(eIF)4E,在mRNA翻译过程中发挥重要作用。这些激酶是丝裂原活化蛋白激酶(MAPK)、细胞外活性调节蛋白激酶(ERK)和p38的下游靶点。利用转基因小鼠品系并通过使用MNK1和MNK2的特异性抑制剂,MNK已被证明与背根神经节和三叉神经节(DRG和TG)外周伤害感受器的敏化有关。虽然该基因的特异性敲除表明它是调节小鼠伤害感受器兴奋性和伤害性行为的关键亚型,但基于RNA测序实验,MNK1和MNK2基因在小鼠和人类的DRG和TG中均有表达。小鼠的单细胞测序表明,MNK1和MNK2可能在不同的伤害感受器群体中表达。我们试图对人类DRG和TG中MNK1和MNK2的mRNA表达进行表征。我们的结果表明,这两个基因在人类两个神经节的几乎所有神经元中均有表达,在其他细胞类型中也有表达。我们的研究结果提供了证据,证明MNK1和MNK2在人类伤害感受器中表达,并表明由于其在两个物种中的保守表达,针对MNK进行疼痛药理学靶向治疗的努力可能具有可转化性。