The Role of lncRNA TUG1 in the Parkinson Disease and Its Effect on Microglial Inflammatory Response

NeuroMolecular Medicine - Tập 23 - Trang 327-334 - 2020
Jiang Cheng1, Yangyang Duan2, Fengting Zhang2, Jin Shi2, Hui Li3, Feng Wang4, Haining Li1
1Department of Neurology, General Hospital of Ningxia Medical University, Ningxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Yinchuan, China
2School of Clinical Medicine, Ningxia Medical University, Yinchuan, China
3Department of Computer Science, Jiangsu Ocean University, Lianyungang, China
4Department of Neurosurgery, General Hospital of Ningxia Medical University, Ningxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Yinchuan, China

Tóm tắt

Parkinson’s disease (PD) is a common neurodegenerative disease in the middle-aged and elderly populations. The purpose of this study was to investigate the clinical value of lncRNA TUG1 in PD and its effect on the microglial inflammatory response. A total of 181 subjects were recruited for the study, including 97 patients with PD (male/female 50/47) and 84 healthy individuals (male/female 41/43). There was no significant difference for gender and age distribution between the groups. The expression of serum TUG1 was determined by qRT-PCR. The receiver operating curve (ROC) was applied for diagnostic value analysis. CCK-8 was used to detect the effect of TUG1 on the proliferation of BV2 cells. The motor coordination ability of mice was tested by the rotarod and pole tests. ELISA was used to detect serum pro-inflammatory factors. TUG1 was highly expressed in the serum of PD patients. Serum TUG1 can distinguish PD patients to form healthy controls with the AUC of 0.902. Serum TUG1 was positively correlated with the levels of UPDRS, IL-6, IL-1β, and TNF-α in PD patients. Cell experiment results showed that the downregulation of TUG1 significantly inhibited cell proliferation and the release of TNF-α, IL-6, and IL-1β. Besides, animal experiments suggested that the downregulation of TUG1 significantly improved the motor coordination ability of the PD mice and inhibited the expression of inflammatory factors. lncRNA TUG1 is a latent biomarker of PD patients. TUG1 downregulation may inhibit the inflammatory response in the progression of PD. These findings provide a possible target for the early diagnosis and therapeutic intervention of PD.

Tài liệu tham khảo

Bachiller, S., Jimenez-Ferrer, I., Paulus, A., Yang, Y., Swanberg, M., Deierborg, T., et al. (2018). Microglia in neurological diseases: A road map to brain-disease dependent-inflammatory response. Frontiers in Cellular Neuroscience, 12, 488. https://doi.org/10.3389/fncel.2018.00488 Bagyinszky, E., Giau, V. V., & An, S. A. (2020). Transcriptomics in Alzheimer’s disease: Aspects and challenges. International Journal of Molecular Sciences, 21(10), 3517. https://doi.org/10.3390/ijms21103517 Chen, H. X., Liang, F. C., Gu, P., Xu, B. L., Xu, H. J., Wang, W. T., et al. (2020). Exosomes derived from mesenchymal stem cells repair a Parkinson’s disease model by inducing autophagy. Cell Death & Disease, 11(4), 288. https://doi.org/10.1038/s41419-020-2473-5 Chen, W., Xu, Z. M., Wang, G., & Chen, S. D. (2012). Non-motor symptoms of Parkinson’s disease in China: A review of the literature. Parkinsonism & Related Disorders, 18(5), 446–452. https://doi.org/10.1016/j.parkreldis.2012.02.002 Derrien, T., Johnson, R., Bussotti, G., Tanzer, A., Djebali, S., Tilgner, H., et al. (2012). The GENCODE v7 catalog of human long noncoding RNAs: Analysis of their gene structure, evolution, and expression. Genome Research, 22(9), 1775–1789. https://doi.org/10.1101/gr.132159.111 Fang, W., Gao, G., Zhao, H., Xia, Y., Guo, X., Li, N., et al. (2015). Role of the Akt/GSK-3beta/CRMP-2 pathway in axon degeneration of dopaminergic neurons resulting from MPP+ toxicity. Brain Research, 1602, 9–19. https://doi.org/10.1016/j.brainres.2014.08.030 Fu, C., Chen, J., Lu, J., Pei, S., Hu, S., Jiang, L., et al. (2019). Downregulation of TUG1 promotes melanogenesis and UVB-induced melanogenesis. Experimental Dermatology, 28(6), 730–733. https://doi.org/10.1111/exd.13929 Han, Y., Liu, Y., Gui, Y., & Cai, Z. (2013). Long intergenic non-coding RNA TUG1 is overexpressed in urothelial carcinoma of the bladder. Journal of Surgical Oncology, 107(5), 555–559. https://doi.org/10.1002/jso.23264 Horvath, I., Iashchishyn, I. A., Moskalenko, R. A., Wang, C., Warmlander, S., Wallin, C., et al. (2018). Co-aggregation of pro-inflammatory S100A9 with alpha-synuclein in Parkinson’s disease: Ex vivo and in vitro studies. Journal of Neuroinflammation, 15(1), 172. https://doi.org/10.1186/s12974-018-1210-9 Hugh-Jones, M. E., Peele, R. H., & Wilson, V. L. (2020). Parkinson’s disease in Louisiana, 1999–2012: Based on hospital primary discharge diagnoses, incidence, and risk in relation to local agricultural crops, pesticides, and aquifer recharge. International Journal of Environmental Research and Public Health, 17(5), 1584. https://doi.org/10.3390/ijerph17051584 Johnson, R. (2012). Long non-coding RNAs in Huntington’s disease neurodegeneration. Neurobiology of Diseases, 46(2), 245–254. https://doi.org/10.1016/j.nbd.2011.12.006 Kim, H. W., Lee, H. S., Kang, J. M., Bae, S. H., Kim, C., Lee, S. H., et al. (2018). Dual effects of human placenta-derived neural cells on neuroprotection and the inhibition of neuroinflammation in a rodent model of Parkinson’s disease. Cell Transplantation, 27(5), 814–830. https://doi.org/10.1177/0963689718766324 Long, T., He, W., Pan, Q., Zhang, S., Zhang, D., Qin, G., et al. (2020). Microglia P2X4R-BDNF signalling contributes to central sensitization in a recurrent nitroglycerin-induced chronic migraine model. The Journal of Headache and Pain, 21(1), 4. https://doi.org/10.1186/s10194-019-1070-4 Mollenhauer, B., Zimmermann, J., Sixel-Doring, F., Focke, N. K., Wicke, T., Ebentheuer, J., et al. (2019). Baseline predictors for progression 4 years after Parkinson’s disease diagnosis in the De Novo Parkinson Cohort (DeNoPa). Movement Disorders, 34(1), 67–77. https://doi.org/10.1002/mds.27492 Neves, K. R., Nobre, H. V., Jr., Leal, L. K., de Andrade, G. M., Brito, G. A., & Viana, G. S. (2015). Pentoxifylline neuroprotective effects are possibly related to its anti-inflammatory and TNF-alpha inhibitory properties, in the 6-OHDA model of Parkinson’s disease. Parkinsons Diseases, 2015, 108179. https://doi.org/10.1155/2015/108179 Nolan, R., & Gaskill, P. J. (2019). The role of catecholamines in HIV neuropathogenesis. Brain Research, 1702, 54–73. https://doi.org/10.1016/j.brainres.2018.04.030 Olmedillas Del Moral, M., Asavapanumas, N., Uzcategui, N. L., & Garaschuk, O. (2019). Healthy brain aging modifies microglial calcium signaling in vivo. International Journal of Molecular Sciences, 20(3), 589. https://doi.org/10.3390/ijms20030589 Santoro, M., Nociti, V., Lucchini, M., Loiodice, M., Centofanti, F., Botta, A., et al. (2020). A pilot study of lncRNAs expression profile in serum of progressive multiple sclerosis patients. European Review for Medical and Pharmacological Sciences, 24(6), 3267–3273. https://doi.org/10.26355/eurrev_202003_20694 Seo, J., Jung, J., Jang, D. S., Kim, J., & Kim, J. H. (2017). Induction of cell death by betulinic acid through induction of apoptosis and inhibition of autophagic flux in microglia BV-2 cells. Biomolecules and Therapeutics (Seoul), 25(6), 618–624. https://doi.org/10.4062/biomolther.2016.255 Wang, H., Liao, S., Li, H., Chen, Y., & Yu, J. (2019). Long non-coding RNA TUG1 sponges Mir-145a-5p to regulate microglial polarization after oxygen-glucose deprivation. Frontiers in Molecular Neuroscience, 12, 215. https://doi.org/10.3389/fnmol.2019.00215 Wang, X. S., Zhang, Z., Wang, H. C., Cai, J. L., Xu, Q. W., Li, M. Q., et al. (2006). Rapid identification of UCA1 as a very sensitive and specific unique marker for human bladder carcinoma. Clinical Cancer Research, 12(16), 4851–4858. https://doi.org/10.1158/1078-0432.CCR-06-0134 Yamada, Y., Shinkawa, K., & Shimmei, K. (2020). Atypical repetition in daily conversation on different days for detecting Alzheimer disease: Evaluation of phone-call data from regular monitoring service. JMIR Mental Health, 7(1), e16790. https://doi.org/10.2196/16790 Ye, J., Sun, H., Feng, Z., Zhang, Q., Xia, Y., Ji, Y., et al. (2019). Prognostic significance of LncRNA GHET1 expression in various cancers: A systematic review and meta-analysis. Bioscience Reports. https://doi.org/10.1042/BSR20190608 Yin, D. D., Zhang, E. B., You, L. H., Wang, N., Wang, L. T., Jin, F. Y., et al. (2015). Downregulation of lncRNA TUG1 affects apoptosis and insulin secretion in mouse pancreatic beta cells. Cellular Physiology and Biochemistry, 35(5), 1892–1904. https://doi.org/10.1159/000373999 Young, T. L., Matsuda, T., & Cepko, C. L. (2005). The noncoding RNA taurine upregulated gene 1 is required for differentiation of the murine retina. Current Biology, 15(6), 501–512. https://doi.org/10.1016/j.cub.2005.02.027 Zhang, Q., Geng, P. L., Yin, P., Wang, X. L., Jia, J. P., & Yao, J. (2013). Down-regulation of long non-coding RNA TUG1 inhibits osteosarcoma cell proliferation and promotes apoptosis. Asian Pacific Journal of Cancer Prevention, 14(4), 2311–2315. https://doi.org/10.7314/apjcp.2013.14.4.2311 Zhao, Z. H., Chen, Z. T., Zhou, R. L., Zhang, X., Ye, Q. Y., & Wang, Y. Z. (2018). Increased DJ-1 and alpha-synuclein in plasma neural-derived exosomes as potential markers for Parkinson’s disease. Frontiers in Aging Neuroscience, 10, 438. https://doi.org/10.3389/fnagi.2018.00438