Choi Hee Joo, Wang Rui, Jakobs Tatjana C
Department of Ophthalmology, Massachusetts Eye and Ear Infirmary/Schepens Eye Research Institute, Harvard Medical School, 20 Staniford Street, Boston, MA, 02114, USA.
Department of Ophthalmology, The First Hospital of Xi'an, Xi'an, Shaanxi, 710002, China.
Methods Mol Biol. 2018;1695:311-334. doi: 10.1007/978-1-4939-7407-8_21.
Recent technological advances have extended the range of analytic tools to very small samples. It is now possible to assay the transcriptome, and in some cases even the proteome, of single cells reliably. This allows addressing novel questions, such as the genotype/phenotype relationships of single neurons, heterogeneity within individual cells of the same type, or the basis of differential vulnerability to injury. An important prerequisite for these kinds of studies is the ability to isolate well-defined individual cells without contamination by adjacent tissue. In the retina and optic nerve, cells of different types and functions are closely intermingled, limiting the use of standard methods such as laser capture microdissection. Here, we describe a simple method to isolate morphologically intact cells from the retina and the optic nerve and discuss considerations in recognizing and isolating different cell types after dissociation.
最近的技术进步已将分析工具的范围扩展到非常小的样本。现在可以可靠地分析单个细胞的转录组,在某些情况下甚至可以分析其蛋白质组。这使得能够解决新的问题,例如单个神经元的基因型/表型关系、同一类型单个细胞内的异质性或对损伤的不同易感性的基础。这类研究的一个重要前提是能够分离出明确的单个细胞而不被相邻组织污染。在视网膜和视神经中,不同类型和功能的细胞紧密交织在一起,限制了激光捕获显微切割等标准方法的使用。在这里,我们描述了一种从视网膜和视神经中分离形态完整细胞的简单方法,并讨论了在解离后识别和分离不同细胞类型时的注意事项。