Sonntag Kai-Christian, Woo Tsung-Ung W
Laboratory for Translational Research on Neurodegeneration, Belmont, MA, United States; Department of Psychiatry, Harvard Medical School, Boston, MA, United States.
Laboratory of Cellular Neuropathology, McLean Hospital, Belmont, MA, United States; Department of Psychiatry, Harvard Medical School, Boston, MA, United States.
Handb Clin Neurol. 2018;150:263-272. doi: 10.1016/B978-0-444-63639-3.00018-9.
Laser microdissection in combination with gene expression profiling using postmortem human brain tissue provides a powerful approach to interrogating cell type-specific pathologies within neural circuits that are known to be dysfunctional in neuropsychiatric disorders. The success of these experiments critically depends on a number of factors, such as the cellular purity of the sample, the quality of the RNA, the methodologies of data normalization and computational data analysis, and how data are interpreted. Data obtained from these experiments should be validated at the protein level. Furthermore, from the perspective of disease mechanism discovery, it would be ideal to investigate whether manipulation of the expression of genes identified as differentially expressed can rescue or ameliorate the neurobiologic or behavioral phenotypes associated with the specific disease. Thus, the ultimate value of this approach rests upon the fact that the generation of novel disease-related pathophysiologic hypotheses may lead to deeper understanding of disease mechanisms and possible development of effective targeted treatments.
结合使用死后人类脑组织进行基因表达谱分析的激光显微切割技术,为探究神经回路中特定细胞类型的病理变化提供了一种强大的方法,这些神经回路在神经精神疾病中已知存在功能障碍。这些实验的成功关键取决于许多因素,例如样本的细胞纯度、RNA的质量、数据标准化和计算数据分析的方法,以及数据的解释方式。从这些实验中获得的数据应在蛋白质水平上进行验证。此外,从疾病机制发现的角度来看,研究对鉴定为差异表达的基因的表达进行操纵是否能够挽救或改善与特定疾病相关的神经生物学或行为表型将是理想的。因此,这种方法的最终价值在于,新的疾病相关病理生理假说的产生可能会导致对疾病机制的更深入理解以及有效靶向治疗的可能发展。