A single-cell sequence analysis of mouse subcutaneous white adipose tissue reveals dynamic changes during weaning.
Shu-Wen QianChenyang ZhangYan TangMengyuan DaiZhihui HeHong MaLinyuan WangQiqi YangYang LiuWei XuZhao ZhangQi-Qun TangPublished in: Communications biology (2024)
Adipose tissue development begins in the fetal period, and continues to expand after birth. Dysregulation of adipose tissue during weaning may predispose individuals to lifelong metabolic disorders. However, the developmental remodeling of adipose tissue during weaning remains largely unexplored. Here we comprehensively compare the changes in mouse subcutaneous white adipose tissue from 7 days after birth to 7 days after weaning using single-cell RNA sequencing along with other molecular and histologic assays. We characterize the developmental trajectory of preadipocytes and indicate the commitment of preadipocytes with beige potential during weaning. Meanwhile, we find immune cells unique to weaning period, whose expression of extracellular matrix proteins implies potential regulation on preadipocyte. Finally, the strongest cell-cell interaction during weaning determined by the TGFβ ligand-receptor pairs is between preadipocytes and endotheliocytes. Our results provide a detailed and unbiased cellular landscape and offer insights into the potential regulation of adipose tissue remodeling during weaning.
Keyphrases
- adipose tissue
- single cell
- mechanical ventilation
- rna seq
- insulin resistance
- high fat diet
- acute respiratory distress syndrome
- extracellular matrix
- high throughput
- intensive care unit
- type diabetes
- poor prognosis
- metabolic syndrome
- cell therapy
- pregnant women
- skeletal muscle
- human health
- epithelial mesenchymal transition
- binding protein
- transforming growth factor
- preterm birth