Fink Ludger, Kwapiszewska Grazyna, Wilhelm Jochen, Bohle Rainer M
Department of Pathology, University of Giessen Lung Center, Langhansstr 10, 35392 Giessen, Germany.
Exp Toxicol Pathol. 2006 Jun;57 Suppl 2:25-9. doi: 10.1016/j.etp.2006.02.010. Epub 2006 Apr 11.
Morphological study and identification of cell differentiation within tissues are the basis for assessment of physiological and pathological processes. Applying molecular techniques, the analysis of tissue homogenates may lead to masking of genetic deviations or expression changes of an individual cell type by the bulk of surrounding cells. To overcome the tissue heterogeneity, cells have to be isolated selectively. Therefore, microdissection techniques were developed making retrieval of target cells simple, rapid and precise. Presenting an overview of our approaches, it is demonstrated that single cell isolation is often preconditional for the investigation of splicing isoform expression. To reveal gene regulation combining microdissection of few cells and real-time RT-PCR allows to determine relative mRNA expression in a cell type-specific manner, even after immunofluorescence staining of target cells. Combination with RNA preamplification techniques and micro arrays results in cell type- or compartment-specific expression profiles that especially differ from those of tissue homogenates when minor represented cell types are investigated. For proteomic biomarker screening, the application of mass spectrometry techniques (SELDI/MALDI TOF) turned out to be feasible in combination with microdissected minute amounts of tissues. However, further identification of marker peaks still needs a remarkable effort. Strategies to deal with this problem are presented. In consequence, the isolation of cells or cell types allows a more accurate investigation of complex tissues and gives deeper insight to regulation processes and crosstalk of the respective cells.
组织内细胞分化的形态学研究与鉴定是评估生理和病理过程的基础。应用分子技术时,组织匀浆分析可能会因大量周围细胞而掩盖个体细胞类型的基因偏差或表达变化。为克服组织异质性,必须选择性地分离细胞。因此,开发了显微切割技术,使靶细胞的获取变得简单、快速且精确。概述我们的方法表明,单细胞分离通常是研究剪接异构体表达的先决条件。为揭示基因调控,将少数细胞的显微切割与实时逆转录聚合酶链反应相结合,即使在对靶细胞进行免疫荧光染色后,也能以细胞类型特异性方式确定相对mRNA表达。与RNA预扩增技术和微阵列相结合,可产生细胞类型或区室特异性表达谱,在研究少量代表性细胞类型时,这些表达谱尤其与组织匀浆的表达谱不同。对于蛋白质组学生物标志物筛选,质谱技术(表面增强激光解吸电离/基质辅助激光解吸电离飞行时间质谱)与显微切割的微量组织相结合被证明是可行的。然而,标记峰的进一步鉴定仍需付出巨大努力。本文提出了解决该问题的策略。因此,细胞或细胞类型的分离能够更准确地研究复杂组织,并更深入地了解各自细胞的调控过程和相互作用。