Department of Biological Sciences, Korea Advanced Institute of Science and Technology, 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, South Korea.
Exp Mol Med. 2020 Nov;52(11):1787-1797. doi: 10.1038/s12276-020-00522-6. Epub 2020 Nov 26.
Aging is associated with gradual deterioration of physiological and biochemical functions, including cognitive decline. Transcriptome profiling of brain samples from individuals of varying ages has identified the whole-transcriptome changes that underlie age-associated cognitive declines. In this review, we discuss transcriptome-based research on human brain aging performed by using microarray and RNA sequencing analyses. Overall, decreased synaptic function and increased immune function are prevalent in most regions of the aged brain. Age-associated gene expression changes are also cell dependent and region dependent and are affected by genotype. In addition, the transcriptome changes that occur during brain aging include different splicing events, intersample heterogeneity, and altered levels of various types of noncoding RNAs. Establishing transcriptome-based hallmarks of human brain aging will improve the understanding of cognitive aging and neurodegenerative diseases and eventually lead to interventions that delay or prevent brain aging.
衰老是生理和生化功能逐渐恶化的过程,包括认知能力下降。对不同年龄段个体的大脑样本进行转录组谱分析,确定了与年龄相关的认知能力下降的全转录组变化。在这篇综述中,我们讨论了使用微阵列和 RNA 测序分析进行的人类大脑衰老的基于转录组的研究。总的来说,在大多数老年人大脑区域,突触功能下降和免疫功能增强是普遍存在的。与年龄相关的基因表达变化也依赖于细胞和区域,并受基因型的影响。此外,大脑衰老过程中发生的转录组变化包括不同的剪接事件、样本间异质性以及各种类型非编码 RNA 水平的改变。建立基于转录组的人类大脑衰老标志将有助于更好地理解认知衰老和神经退行性疾病,并最终导致延缓或预防大脑衰老的干预措施的出现。