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脑卒中后恢复相关基因在小鼠中的时空表达谱。

Temporal and Spatial Gene Expression Profile of Stroke Recovery Genes in Mice.

机构信息

Faculty of Medicine, University of Cologne, 50923 Cologne, Germany.

Department of Neurology, University Hospital Cologne, 50931 Cologne, Germany.

出版信息

Genes (Basel). 2023 Feb 9;14(2):454. doi: 10.3390/genes14020454.

DOI:10.3390/genes14020454
PMID:36833381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9956317/
Abstract

Stroke patients show some degree of spontaneous functional recovery, but this is not sufficient to prevent long-term disability. One promising approach is to characterize the dynamics of stroke recovery genes in the lesion and distant areas. We induced sensorimotor cortex lesions in adult C57BL/6J mice using photothrombosis and performed qPCR on selected brain areas at 14, 28, and 56 days post-stroke (P14-56). Based on the grid walk and rotating beam test, the mice were classified into two groups. The expression of cAMP pathway genes , , and , was higher in poor- compared to well-recovered mice in contralesional primary motor cortex (cl-MOp) at P14&56 and cl-thalamus (cl-TH), but lower in cl-striatum (cl-Str) at P14 and cl-primary somatosensory cortex (cl-SSp) at P28. Plasticity and axonal sprouting genes, and , were decreased in cl-MOp at P14 and cl-Str at P28 and increased in cl-SSp at P28 and cl-Str at P14, respectively. In the cl-TH, was increased, and decreased at P14. , also involved in axonal sprouting, was only increased in poor-recovered mice in cl-MOp at P28. The results underline the gene expression dynamics and spatial variability and challenge existing theories of restricted neural plasticity.

摘要

中风患者表现出一定程度的自发性功能恢复,但这不足以防止长期残疾。一种有前途的方法是描述病变和远处区域中风恢复基因的动力学。我们使用光血栓形成在成年 C57BL/6J 小鼠中诱导感觉运动皮层损伤,并在中风后 14、28 和 56 天(P14-56)对选定的大脑区域进行 qPCR。根据网格行走和旋转梁测试,将小鼠分为两组。在 P14 和 P28 的 cl-Str 和 P14 的 cl-SSp 中,在 P14 和 P56 的 cl-MOp 和 cl-TH 中,与恢复良好的小鼠相比,cAMP 通路基因 、 和 在对侧运动皮层(cl-MOp)和对侧丘脑(cl-TH)中的表达更高,但在 P14 的 cl-Str 和 P28 的 cl-SSp 中表达较低。可塑性和轴突发芽基因 、 和 在 P14 的 cl-MOp 和 P28 的 cl-Str 中降低,在 P28 的 cl-SSp 和 P14 的 cl-Str 中增加。在 cl-TH 中, 在 P14 时增加, 在 P14 时减少。 ,也参与轴突发芽,仅在 P28 的 cl-MOp 中恢复不佳的小鼠中增加。这些结果强调了基因表达的动态变化和空间变异性,挑战了现有的神经可塑性受限理论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/d7bb4cda7196/genes-14-00454-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/89e325b6b95c/genes-14-00454-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/ecc7e62bff70/genes-14-00454-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/08c378aabfbf/genes-14-00454-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/501b6497d959/genes-14-00454-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/477f19f88f9e/genes-14-00454-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/d7bb4cda7196/genes-14-00454-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/89e325b6b95c/genes-14-00454-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/539852a18b91/genes-14-00454-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/ecc7e62bff70/genes-14-00454-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/08c378aabfbf/genes-14-00454-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/501b6497d959/genes-14-00454-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/477f19f88f9e/genes-14-00454-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f97/9956317/d7bb4cda7196/genes-14-00454-g007.jpg

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