Wang Changsheng, Chen Rongsheng, Zhu Xitian, Zhang Xiaobo, Lian Nancheng
Department of Spinal Surgery, First Affiliated Hospital of Fujian Medical University, No. 20 Chazhong Road, Taijiang District, Fuzhou, 350005, Fujian, People's Republic of China.
Hum Cell. 2024 Mar;37(2):451-464. doi: 10.1007/s13577-023-01019-w. Epub 2024 Jan 2.
This study aims to explore the functions and mechanisms of long noncoding RNA small nucleolar RNA host gene 5 (SNHG5) in chronic constriction injury (CCI)-induced neuropathic pain (NP). An NP rat model was established using the CCI method and the NP severity was evaluated by paw withdrawal threshold (PWT) and paw withdrawal latency (PWL). The expression of SNHG5, CDK9, and SCN9A was quantified in rat dorsal root ganglion, in addition to the detections of apoptosis, pathological changes, neuron number, and the co-localization of Nav1.7 and cleaved caspase-3 with NeuN. In ND7/23 cells, the apoptosis and lactate dehydrogenase concentration were assessed, as well as the relationship between SNHG5, CDK9, and SCN9A. In the dorsal root ganglion of CCI-treated rats, SNHG5 and SCN9A were upregulated and downregulation of SNHG5 suppressed SCN9A expression, increased the PWT and PWL, blocked neuroinflammation and neuronal apoptosis, and alleviated NP. Mechanistically, SNHG5 recruited CDK9 to enhance SCN9A-encoded Nav1.7 expression and promoted peripheral neuronal apoptosis and injury. In addition, SCN9A overexpression nullified the alleviative effects of SNHG5 deficiency on NP and neuron loss in CCI rats. In conclusion, SNHG5 promotes SCN9A-encoded Nav1.7 expression by recruiting CDK9, thereby facilitating neuron loss and NP after spinal nerve injury, which may offer a promising target for the management of NP.
本研究旨在探讨长链非编码RNA小核仁RNA宿主基因5(SNHG5)在慢性压迫性损伤(CCI)诱导的神经性疼痛(NP)中的作用及机制。采用CCI法建立NP大鼠模型,并通过爪部缩足阈值(PWT)和爪部缩足潜伏期(PWL)评估NP严重程度。除检测细胞凋亡、病理变化、神经元数量以及Nav1.7和裂解的半胱天冬酶-3与NeuN的共定位外,还对大鼠背根神经节中SNHG5、细胞周期蛋白依赖性激酶9(CDK9)和电压门控钠通道9(SCN9A)的表达进行了定量分析。在ND7/23细胞中,评估了细胞凋亡和乳酸脱氢酶浓度,以及SNHG5、CDK9和SCN9A之间的关系。在CCI处理大鼠的背根神经节中,SNHG5和SCN9A上调,SNHG5下调抑制SCN9A表达,增加PWT和PWL,阻断神经炎症和神经元凋亡,减轻NP。机制上,SNHG5募集CDK9以增强SCN9A编码的Nav1.7表达,促进外周神经元凋亡和损伤。此外,SCN9A过表达消除了SNHG5缺陷对CCI大鼠NP和神经元丢失的缓解作用。总之,SNHG5通过募集CDK9促进SCN9A编码的Nav1.7表达,从而促进脊神经损伤后神经元丢失和NP,这可能为NP的治疗提供一个有前景的靶点。