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Inhibition by rno-circRNA-013017 of the apoptosis of motor neurons in anterior horn and descending axonal degeneration in rats after traumatic spinal cord injury.
Qin, Chuan; Liu, Yi; Xu, Pei-Pei; Zhang, Xin; Talifu, Zuliyaer; Liu, Jia-Yi; Jing, Ying-Li; Bai, Fan; Zhao, Li-Xi; Yu, Yan; Gao, Feng; Li, Jian-Jun.
Afiliación
  • Qin C; Department of Urology, Beijing Friendship Hospital, Beijing, China.
  • Liu Y; School of Rehabilitation Medicine, Capital Medical University, Beijing, China.
  • Xu PP; China Rehabilitation Science Institute, Beijing, China.
  • Zhang X; Center of Neural Injury and Repair, Beijing Institute for Brain Disorders, Beijing, China.
  • Talifu Z; Department of Spinal and Neural Functional Reconstruction, China Rehabilitation Research Center, Beijing, China.
  • Liu JY; Beijing Key Laboratory of Neural Injury and Rehabilitation, Beijing, China.
  • Jing YL; School of Rehabilitation Medicine, Capital Medical University, Beijing, China.
  • Bai F; Center of Neural Injury and Repair, Beijing Institute for Brain Disorders, Beijing, China.
  • Zhao LX; Department of Spinal and Neural Functional Reconstruction, China Rehabilitation Research Center, Beijing, China.
  • Yu Y; Beijing Key Laboratory of Neural Injury and Rehabilitation, Beijing, China.
  • Gao F; Department of Rehabilitation Medicine, The Second Hospital of Anhui Medical University, Hefei, China.
  • Li JJ; School of Rehabilitation Medicine, Capital Medical University, Beijing, China.
Front Neurosci ; 16: 1065897, 2022.
Article en En | MEDLINE | ID: mdl-36590290
ABSTRACT

Introduction:

Spinal cord injury (SCI) often causes continuous neurological damage to clinical patients. Circular RNAs (circRNAs) are related to a lot of diseases, including SCI. We previously found five candidate circRNAs which were likely to regulate the secondary pathophysiological changes in rat model after traumatic SCI.

Methods:

In this study, we first selected and overexpressed target circRNA in rats. We then explored its functional roles using various functional assays in a rat model after SCI.

Results:

We found that rno-circRNA-013017-the selected target circRNA-reduced neuron apoptosis, preserved the survival and activity of motor neurons, and regulated apoptosis-related proteins at 3 days post-SCI using western blot, immunofluorescence and polymerase chain reaction. Additionally, we found that rno-circRNA-013017 inhibited descending axonal degeneration and preserved motor neurons and descending axons at 6 weeks post-SCI using immunofluorescence, biotin dextran amine diffusion tensor imaging. Finally, the overexpression of rno-circRNA-013017 promoted the locomotor function of rats after SCI using open-field test and gait analysis.

Conclusion:

Focusing on the functions of rno-circRNA-013017, this study provides new options for future studies exploring therapeutic targets and molecular mechanisms for SCI.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2022 Tipo del documento: Article País de afiliación: China