Murtie Joshua C, Macklin Wendy B, Corfas Gabriel
Division of Neuroscience, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Neurosci Res. 2007 Aug 1;85(10):2080-6. doi: 10.1002/jnr.21339.
Oligodendrocytes (OLs), the myelinating cells of the central nervous system, have specialized morphologies that subserve their function. Numerous qualitative studies suggest that OLs in different brain regions can differ in their morphological characteristics, including number of branches and internodes, internode length, etc. However, progress in identifying and characterizing the diverse types of OLs and their distribution in the brain has been made difficult by several technical constraints. Here we report a new strategy to analyze OL morphology with a high degree of quantitative power and throughput. We used confocal microscopy and three-dimensional cell tracing software to study OLs in the frontal cortex of mice expressing enhanced green fluorescent protein (eGFP) under the control of the proteolipid protein (Plp) gene promoter. Three-dimensional reconstructions were then used to analyze and quantify cell morphology, including total process length, total process surface area, total internode length, number of primary processes, number of branch points, and number of internodes. In addition, these reconstructions were subjected to Sholl analysis, which allows for the quantitative measure of OL arbor complexity. By using this approach, we identified and characterized a previously undescribed population of small OLs with a compact but complex morphology that includes numerous branching processes and a large number of short internodes. Our data suggest that other populations of OLs remain to be identified and characterized and that the tools we have developed could help in the process of characterizing them.
少突胶质细胞(OLs)是中枢神经系统的髓鞘形成细胞,具有专门的形态以履行其功能。大量定性研究表明,不同脑区的少突胶质细胞在形态特征上可能存在差异,包括分支数量、节间数量、节间长度等。然而,由于一些技术限制,在识别和表征不同类型的少突胶质细胞及其在大脑中的分布方面进展困难。在此,我们报告一种新策略,可高度定量且高通量地分析少突胶质细胞形态。我们使用共聚焦显微镜和三维细胞追踪软件来研究在蛋白脂蛋白(Plp)基因启动子控制下表达增强型绿色荧光蛋白(eGFP)的小鼠额叶皮质中的少突胶质细胞。然后利用三维重建来分析和量化细胞形态,包括总突起长度、总突起表面积、总结间长度、初级突起数量、分支点数量和节间数量。此外,对这些重建进行了肖尔分析,该分析可对少突胶质细胞树突复杂性进行定量测量。通过使用这种方法,我们识别并表征了一群以前未描述过的小型少突胶质细胞,其形态紧凑但复杂,包括许多分支突起和大量短节间。我们的数据表明,其他少突胶质细胞群体仍有待识别和表征,并且我们开发的工具可能有助于这一表征过程。