Neural cell diversity in the light of single-cell transcriptomics

被引:3
作者
Fernandez-Moya, Sandra Maria [1 ,2 ,4 ]
Ganesh, Akshay Jaya [1 ,2 ]
Plass, Mireya [1 ,2 ,3 ,4 ]
机构
[1] Bellvitge Inst Biomed Res IDIBELL, Regenerat Med Program, Gene Regulat Cell Ident, Barcelona, Spain
[2] Program Adv Clin Translat Regenerat Med Catalonia, Barcelona, Spain
[3] Ctr Networked Biomed Res Bioengn Biomat & Nanomed, Madrid, Spain
[4] Bellvitge Inst Biomed Res IDIBELL, Regenerat Med Program, Gene Regulat Cell Ident, Barcelona 08908, Spain
来源
TRANSCRIPTION-AUSTIN | 2023年 / 14卷 / 3-5期
关键词
Cell diversity; single-cell transcriptomics; neural cells; brain; gene regulatory networks; RNA-SEQ; CHROMATIN; ATLAS; NEURONS; PROTEINS; SUBTYPES; DORSAL; MOUSE;
D O I
10.1080/21541264.2023.2295044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of highly parallel and affordable high-throughput single-cell transcriptomics technologies has revolutionized our understanding of brain complexity. These methods have been used to build cellular maps of the brain, its different regions, and catalog the diversity of cells in each of them during development, aging and even in disease. Now we know that cellular diversity is way beyond what was previously thought. Single-cell transcriptomics analyses have revealed that cell types previously considered homogeneous based on imaging techniques differ depending on several factors including sex, age and location within the brain. The expression profiles of these cells have also been exploited to understand which are the regulatory programs behind cellular diversity and decipher the transcriptional pathways driving them. In this review, we summarize how single-cell transcriptomics have changed our view on the cellular diversity in the human brain, and how it could impact the way we study neurodegenerative diseases. Moreover, we describe the new computational approaches that can be used to study cellular differentiation and gain insight into the functions of individual cell populations under different conditions and their alterations in disease.
引用
收藏
页码:158 / 176
页数:19
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