Hu Jian-Zhong, Rong Zi-Jie, Li Miao, Li Ping, Jiang Li-Yuan, Luo Zi-Xiang, Duan Chun-Yue, Cao Yong, Lu Hong-Bin
Department of Spine Surgery, Xiangya Hospital, Central South University, Changsha, China.
Key Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Xiangya Hospital, Central South University, Changsha, China.
Front Cell Neurosci. 2019 Feb 20;13:50. doi: 10.3389/fncel.2019.00050. eCollection 2019.
Neuropathic pain (NP) is among the most intractable comorbidities of spinal cord injury. Dysregulation of non-coding RNAs has also been implicated in the development of neuropathic pain. Here, we identified a novel lncRNA, PKIA-AS1, by using lncRNA array analysis in spinal cord tissue of spinal nerve ligation (SNL) model rats, and investigated the role of PKIA-AS1 in SNL-mediated neuropathic pain. We observed that PKIA-AS1 was significantly upregulated in SNL model rats and that PKIA-AS1 knockdown attenuated neuropathic pain progression. Alternatively, overexpression of PKIA-AS1 was sufficient to induce neuropathic pain-like symptoms in uninjured rats. We also found that PKIA-AS1 mediated SNL-induced neuropathic pain by directly regulating the expression and function of CDK6, which is essential for the initiation and maintenance of neuroinflammation and neuropathic pain. Therefore, our study identifies PKIA-AS1 as a novel therapeutic target for neuroinflammation related neuropathic pain.
神经性疼痛(NP)是脊髓损伤最棘手的合并症之一。非编码RNA的失调也与神经性疼痛的发生有关。在此,我们通过对脊髓神经结扎(SNL)模型大鼠脊髓组织进行lncRNA阵列分析,鉴定出一种新型lncRNA,即PKIA-AS1,并研究了PKIA-AS1在SNL介导的神经性疼痛中的作用。我们观察到PKIA-AS1在SNL模型大鼠中显著上调,并且PKIA-AS1基因敲低可减轻神经性疼痛的进展。另外,PKIA-AS1的过表达足以在未受伤的大鼠中诱导出神经性疼痛样症状。我们还发现PKIA-AS1通过直接调节CDK6的表达和功能来介导SNL诱导的神经性疼痛,而CDK6对于神经炎症和神经性疼痛的起始和维持至关重要。因此,我们的研究将PKIA-AS1确定为神经炎症相关神经性疼痛的新型治疗靶点。