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Laser-Capture Microdissection a Tool for the Global Analysis of Gene Expression in Specific Plant Cell Types

机译:激光捕获显微切割术一种用于分析特定植物细胞类型中基因表达的整体工具

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摘要

Laser-capture microdissection (LCM) allows for the one-step procurement of large homogeneous populations of cells from tissue sections. In mammals, LCM has been used to conduct cDNA microarray and proteomics studies on specific cell types. However, LCM has not been applied to plant cells, most likely because plant cell walls make it difficult to separate target cells from surrounding cells and because ice crystals can form in the air spaces between cells when preparing frozen sections. By fixing tissues, using a cryoprotectant before freezing, and using an adhesive-coated slide system, it was possible to capture large numbers (>10,000) of epidermal cells and vascular tissues (vascular bundles and bundle sheath cells) from ethanol:acetic acid–fixed coleoptiles of maize. RNA extracted from these cells was amplified with T7 RNA polymerase and used to hybridize a microarray containing ∼8800 maize cDNAs. Approximately 250 of these were expressed preferentially in epidermal cells or vascular tissues. These results demonstrate that the combination of LCM and microarrays makes it feasible to conduct high-resolution global gene expression analyses of plants. This approach has the potential to enhance our understanding of diverse plant cell type–specific biological processes.
机译:激光捕获显微切割(LCM)允许从组织切片中一步采购大量均匀的细胞。在哺乳动物中,LCM已用于对特定细胞类型进行cDNA微阵列和蛋白质组学研究。但是,LCM尚未应用于植物细胞,这很可能是因为植物细胞壁难以将靶细胞与周围细胞分离,并且在制备冷冻切片时细胞之间的空隙中会形成冰晶。通过固定组织,在冷冻前使用冷冻保护剂以及使用粘合剂涂层的载玻片系统,可以从乙醇:乙酸中捕获大量(> 10,000)表皮细胞和血管组织(血管束和束鞘细胞)–固定玉米胚芽鞘。用T7 RNA聚合酶扩增从这些细胞中提取的RNA,并用于杂交含有约8800个玉米cDNA的微阵列。其中约250个优先在表皮细胞或血管组织中表达。这些结果证明,LCM和微阵列的结合使得进行植物的高分辨率全局基因表达分析是可行的。这种方法有可能加深我们对特定植物细胞类型特异性生物过程的理解。

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