Department of Molecular & Integrative Physiology, Kansas University Medical Center, Kansas City, KS 66160, USA.
Mol Cell Biochem. 2012 Oct;369(1-2):267-86. doi: 10.1007/s11010-012-1390-z. Epub 2012 Jul 21.
After cortical injury resulting from stroke, some recovery can occur and may involve spared areas of the cerebral cortex reorganizing to assume functions previously controlled by the damaged cortical areas. No studies have specifically assessed gene expression changes in remote neurons with axonal processes that terminate in the infarcted tissue, i.e., the subset of neurons most likely to be involved in regenerative processes. By physiologically identifying the primary motor area controlling forelimb function in adult rats (caudal forelimb area = CFA), and injecting a retrograde tract-tracer, we labeled neurons within the non-primary motor cortex (rostral forelimb area = RFA) that project to CFA. Then, 7 days after a CFA infarct (n = 6), we used laser capture microdissection techniques to harvest labeled neurons in RFA. Healthy, uninjured rats served as controls (n = 6). Biological interactions and functions of gene profiling were investigated by Affymetrix Microarray, and Ingenuity Pathway Analysis. A total of 143 up- and 128 down-regulated genes showed significant changes (fold change ≥1.3 and p < 0.05). The canonical pathway, "Axonal Guidance Signaling," was overrepresented (p value = 0.002). Significantly overrepresented functions included: branching of neurites, organization of cytoskeleton, dendritic growth and branching, organization of cytoplasm, guidance of neurites, development of cellular protrusions, density of dendritic spines, and shape change (p = 0.000151-0.0487). As previous studies have shown that spared motor areas are important in recovery following injury to the primary motor area, the results suggest that these gene expression changes in remote, interconnected neurons may underlie reorganization and recovery mechanisms.
在中风导致皮质损伤后,一些恢复可能会发生,并且可能涉及大脑皮质的未受损区域重新组织,以承担以前由受损皮质区域控制的功能。没有研究专门评估轴突过程终末于梗塞组织中的远程神经元的基因表达变化,即最有可能参与再生过程的神经元亚群。通过生理上确定控制成年大鼠前肢功能的初级运动区(后肢区= CFA),并注射逆行示踪剂,我们标记了投射到 CFA 的非初级运动皮层(前肢区= RFA)内的神经元。然后,在 CFA 梗塞后 7 天(n = 6),我们使用激光捕获显微解剖技术收获 RFA 中的标记神经元。健康,未受伤的大鼠作为对照(n = 6)。通过 Affymetrix 微阵列和 Ingenuity 通路分析研究了基因谱的生物学相互作用和功能。总共发现 143 个上调和 128 个下调基因显示出显着变化(倍数变化≥1.3 和 p <0.05)。“轴突导向信号”的经典途径被过度表示(p 值= 0.002)。显著过度表示的功能包括:神经突分支,细胞骨架组织,树突生长和分支,细胞质组织,神经突导向,细胞突起的发育,树突棘密度和形状变化(p = 0.000151-0.0487)。如先前的研究表明,在初级运动区损伤后,未受损的运动区在恢复中很重要,因此结果表明,这些远程,相互连接的神经元中的基因表达变化可能是重新组织和恢复机制的基础。