Isolation of Adipose Tissue Nuclei for Single-Cell Genomic Applications

被引:7
|
作者
Benitez, Gabrielle J. [1 ]
Shinoda, Kosaku [1 ,2 ,3 ]
机构
[1] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
[2] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10467 USA
[3] Fleischer Inst Diabet & Metab, Bronx, NY 10461 USA
来源
基金
美国国家卫生研究院;
关键词
MESSENGER-RNA; BROWN;
D O I
10.3791/61230
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Brown and beige fat are specialized adipose tissues that dissipate energy for thermogenesis by UCP1 (Uncoupling Protein-1)-dependent and independent pathways. Until recently, thermogenic adipocytes were considered a homogeneous population. However, recent studies have indicated that there are multiple subtypes or subpopulations that are distinct in developmental origin, substrate use, and transcriptome. Despite advances in single-cell genomics, unbiased decomposition of adipose tissues into cellular subtypes has been challenging because of the fragile nature of lipid-filled adipocytes. The protocol presented was developed to circumvent these obstacles by effective isolation of single nuclei from adipose tissue for downstream applications, including RNA sequencing. Cellular heterogeneity can then be analyzed by RNA sequencing and bioinformatic analyses.
引用
收藏
页码:1 / 9
页数:9
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