Harrison Benjamin J, Venkat Gayathri, Hutson Thomas, Rau Kristofer K, Bunge Mary Bartlett, Mendell Lorne M, Gage Fred H, Johnson Richard D, Hill Caitlin, Rouchka Eric C, Moon Lawrence, Petruska Jeffrey C
Department of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40202, United States ; Kentucky Spinal Cord Injury Research Center (KSCIRC), University of Louisville, Louisville, KY 40202, United States ; Kentucky Biomedical Research Infrastructure Network Bioinformatics Core, University of Louisville, Louisville, KY 40292, United States.
Department of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40202, United States ; Kentucky Spinal Cord Injury Research Center (KSCIRC), University of Louisville, Louisville, KY 40202, United States.
Genom Data. 2015 Oct 23;6:249-52. doi: 10.1016/j.gdata.2015.10.005. eCollection 2015 Dec.
Primary afferent collateral sprouting is a process whereby non-injured primary afferent neurons respond to some stimulus and extend new branches from existing axons. Neurons of both the central and peripheral nervous systems undergo this process, which contributes to both adaptive and maladaptive plasticity (e.g., [1], [2], [3], [4], [5], [6], [7], [8], [9]). In the model used here (the "spared dermatome" model), the intact sensory neurons respond to the denervation of adjacent areas of skin by sprouting new axon branches into that adjacent denervated territory. Investigations of gene expression changes associated with collateral sprouting can provide a better understanding of the molecular mechanisms controlling this process. Consequently, it can be used to develop treatments to promote functional recovery for spinal cord injury and other similar conditions. This report includes raw gene expression data files from microarray experiments in order to study the gene regulation in spared sensory ganglia in the initiation (7 days) and maintenance (14 days) phases of the spared dermatome model relative to intact ("naïve") sensory ganglia. Data has been deposited into GEO (GSE72551).
初级传入侧支发芽是一个过程,在此过程中未受损的初级传入神经元对某种刺激做出反应,并从现有的轴突延伸出新的分支。中枢神经系统和外周神经系统的神经元都会经历这个过程,它有助于适应性和适应不良性可塑性(例如,[1]、[2]、[3]、[4]、[5]、[6]、[7]、[8]、[9])。在本文使用的模型(“保留皮节”模型)中,完整的感觉神经元通过向相邻的去神经支配区域长出新的轴突分支来对相邻皮肤区域的去神经支配做出反应。对与侧支发芽相关的基因表达变化的研究可以更好地理解控制这一过程的分子机制。因此,它可用于开发促进脊髓损伤和其他类似病症功能恢复的治疗方法。本报告包括来自微阵列实验的原始基因表达数据文件,以便研究在“保留皮节”模型的起始阶段(7天)和维持阶段(14天)相对于完整(“未处理”)感觉神经节的保留感觉神经节中的基因调控。数据已存入基因表达综合数据库(GSE72551)。