Genetic dissection of intercellular interactions in vivo by membrane-permeable protein.
Shaohua ZhangQianyu ZhangZixin LiuKuo LiuLingjuan HeKathy O LuiLi-Xin WangBin ZhouPublished in: Proceedings of the National Academy of Sciences of the United States of America (2022)
Unraveling cell-cell interaction is fundamental to understanding many biological processes. To date, genetic tools for labeling neighboring cells in mammals are not available. Here, we developed a labeling strategy based on the Cre-induced intercellular labeling protein (CILP). Cre-expressing donor cells release a lipid-soluble and membrane-permeable fluorescent protein that is then taken up by recipient cells, enabling fluorescent labeling of neighboring cells. Using CILP, we specifically labeled endothelial cells surrounding a special population of hepatocytes in adult mice and revealed their distinct gene signatures. Our results highlight the potential of CILP as a platform to reveal cell-cell interactions and communications in vivo.
Keyphrases
- induced apoptosis
- single cell
- cell cycle arrest
- endothelial cells
- genome wide
- cell therapy
- endoplasmic reticulum stress
- copy number
- stem cells
- cell death
- high glucose
- oxidative stress
- computed tomography
- quantum dots
- signaling pathway
- adipose tissue
- metabolic syndrome
- risk assessment
- transcription factor
- skeletal muscle
- living cells
- cell proliferation
- drug induced
- single molecule