Dynamic Expression Pattern of Neuro-oncological Ventral Antigen 1 (Nova1) in the Rat Brain after Focal Cerebral Ischemia/Reperfusion Insults

Author:

Li Hualing1234,Sun Changqing1234,Wang Yu1234,Gao Yuxiao1234,Liu Yichen1234,Gao Yan1234,Li Xu1234,Zhang Chenggang1234

Affiliation:

1. Beijing Institute of Radiation Medicine, State Key Laboratory of Proteomics, State Key Laboratory of Medical Neurobiology, Cognitive and Mental Health Research Center, Beijing, China (HL, CS, YW, YuxiaoG, YL, YanG, CZ)

2. Department of Biochemistry and Molecular Biology, Medical College of Yangzhou University, Jiangsu, China (HL)

3. Department of Neurosurgery, Tianjin Baodi Hospital, Tianjin, China (CS)

4. Medical Laboratory Center of the First Affiliated Hospital, Medical School of Xi’an Jiaotong University, Xi’an, China (YW,XL)

Abstract

The present study aimed to evaluate the expression of neuro-oncological ventral antigen 1 (Nova1) in cerebral ischemia/reperfusion (I/R) insults by immunohistochemistry. The focal cerebral I/R model was induced by right middle cerebral artery occlusion (MCAO) for 120 min followed by 1 day, 7 days, and 14 days of reperfusion in Sprague-Dawley (SD) rats. The results showed that Nova1 was expressed in nearly the whole brain, although with higher density in hippocampus, hypothalamus, cingulate cortex, and medial habenular nucleus. The immunoreactivity of Nova1 neurons was increased dramatically, especially on both sides of the hippocampal CA1 region, after 1 day of reperfusion. A strong response occurred at the ipsilateral CA1 region between 1 day and 7 days of reperfusion. Likewise, strong compensatory responses of Nova1 expression were observed on the contralateral side of the striate cortex, dentate gyrus, and hypothalamus. Interestingly, more Nova1 neurons were observed to translocate to the dendrites and growth cones of the axons in the hypothalamus on the ischemic side after 7 days of reperfusion. In conclusion, our data suggest that Nova1 might mediate neuronal responsiveness, and its expression might positively correlate with neural repair after I/R insults in the rat brain.

Publisher

SAGE Publications

Subject

Histology,Anatomy

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