Theranostics 2021; 11(4):1814-1827. doi:10.7150/thno.51550 This issue Cite

Research Paper

Retina as a window to cerebral dysfunction following studies with circRNA signature during neurodegeneration

Qin Jiang1,2*, Dong-Yuan Su3*, Zhen-Zhen Wang1,2*, Chang Liu1,2*, Ya-Nan Sun4, Hong Cheng5, Xiu-Miao Li1, Biao Yan4,6✉

1. The Affiliated Eye Hospital, Nanjing Medical University, Nanjing, China.
2. The Fourth School of Clinical Medicine, Nanjing Medical University, Nanjing, China.
3. Jiangsu Province Key Laboratory of Neurodegeneration, Center for Global Health, Nanjing Medical University, Nanjing, China.
4. Eye Institute, Eye & ENT Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
5. Department of Neurology, Jiangsu Province Hospital, Nanjing, China.
6. NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, and Shanghai Key Laboratory of Visual Impairment and Restoration (Fudan University), Shanghai, China.
*These authors contributed equally to this work.

Citation:
Jiang Q, Su DY, Wang ZZ, Liu C, Sun YN, Cheng H, Li XM, Yan B. Retina as a window to cerebral dysfunction following studies with circRNA signature during neurodegeneration. Theranostics 2021; 11(4):1814-1827. doi:10.7150/thno.51550. https://www.thno.org/v11p1814.htm
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Abstract

Graphic abstract

Ischemia-induced cerebral injury is a major cause of dementia or death worldwide. The pre-diagnosis is still challenging due to the retarded symptoms. The retina is regarded as the extension of cerebral tissue. Circular RNAs have emerged as the crucial regulators in gene regulatory network and disease progression. However, it is still unknown whether circRNAs can be used as the common regulators and diagnostic markers for cerebral neurodegeneration and retinal neurodegeneration.

Methods: C57BL/6J mice were subjected to transient middle cerebral artery occlusion and circRNA microarray profiling was performed to identify neurodegeneration-related circRNAs. Quantitative reverse-transcription PCR (qRT-PCR) assays were performed to verify circRNA expression pattern. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis was performed to determine the biologic modules and signaling pathway. TTC staining, Nissl's staining, and immunofluorescence staining assays were performed to investigate the role of circRNA in cerebral neurodegeneration and retinal neurodegeneration in vivo. MTT assay, Propidium iodide (PI)/Calcein-AM staining, and Rhodamine 123 assays were performed to investigate the role of circRNA in neuronal injury in vitro. Bioinformatics, RIP, and luciferase activity assays were performed to determine the regulatory mechanism of circRNA in neurodegeneration.

Results: 217 differentially expressed circRNAs were identified between ischemic cerebral tissues and normal controls. Among them, cGLIS3 was shown as the common regulator of cerebral neurodegeneration and retinal neurodegeneration. cGLIS3 silencing alleviated ischemia-induced retinal neurodegeneration and MCAO-induced cerebral neurodegeneration in vivo. cGLIS3 silencing protected against OGD/R-induced RGC injury in vitro. The circulating levels of cGLIS3 were significantly increased in the patients with ischemic stroke compared to healthy subjects. cGLIS3 levels were also increased in the aqueous humor of the patients with retinal vein occlusion. cGLIS3 regulated neuronal cell injury by acting as miR-203 sponge and its level was controlled by EIF4A3.

Conclusions: This study provides molecular evidence that the retina is window of the brain from circRNA perspective. cGLIS3 is a common regulator and diagnostic marker of cerebral neurodegeneration and retinal neurodegeneration.

Keywords: Circular RNAs, Ischemia, MCAO, OGD/R, retinal neurodegeneration


Citation styles

APA
Jiang, Q., Su, D.Y., Wang, Z.Z., Liu, C., Sun, Y.N., Cheng, H., Li, X.M., Yan, B. (2021). Retina as a window to cerebral dysfunction following studies with circRNA signature during neurodegeneration. Theranostics, 11(4), 1814-1827. https://doi.org/10.7150/thno.51550.

ACS
Jiang, Q.; Su, D.Y.; Wang, Z.Z.; Liu, C.; Sun, Y.N.; Cheng, H.; Li, X.M.; Yan, B. Retina as a window to cerebral dysfunction following studies with circRNA signature during neurodegeneration. Theranostics 2021, 11 (4), 1814-1827. DOI: 10.7150/thno.51550.

NLM
Jiang Q, Su DY, Wang ZZ, Liu C, Sun YN, Cheng H, Li XM, Yan B. Retina as a window to cerebral dysfunction following studies with circRNA signature during neurodegeneration. Theranostics 2021; 11(4):1814-1827. doi:10.7150/thno.51550. https://www.thno.org/v11p1814.htm

CSE
Jiang Q, Su DY, Wang ZZ, Liu C, Sun YN, Cheng H, Li XM, Yan B. 2021. Retina as a window to cerebral dysfunction following studies with circRNA signature during neurodegeneration. Theranostics. 11(4):1814-1827.

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