Endothelial cell heterogeneity and microglia regulons revealed by a pig cell landscape at single-cell level.
Fei WangPeiwen DingXue LiangXiangning DingCamilla Blunk BrandtEvelina SjöstedtJiacheng ZhuSaga BolundLijing ZhangLaura P M H de RooijLihua LuoYanan WeiWandong ZhaoZhiyuan LvJános HaskóRunchu LiQiuyu QinYi JiaWendi WuYuting YuanMingyi PuHaoyu WangAiping WuLin XiePing LiuFang ChenJacqueline HeroldJoanna M KaluckaMax J KarlssonXiuqing ZhangRikke Bek HelmigLinn FagerbergCecilia LindskogFrederik PonténMathias UhlenLars BolundNiels JessenHui JiangXue LiuHuanming YangPeter CarmelietJan MulderDongsheng ChenLin LinYonglun LuoPublished in: Nature communications (2022)
Pigs are valuable large animal models for biomedical and genetic research, but insights into the tissue- and cell-type-specific transcriptome and heterogeneity remain limited. By leveraging single-cell RNA sequencing, we generate a multiple-organ single-cell transcriptomic map containing over 200,000 pig cells from 20 tissues/organs. We comprehensively characterize the heterogeneity of cells in tissues and identify 234 cell clusters, representing 58 major cell types. In-depth integrative analysis of endothelial cells reveals a high degree of heterogeneity. We identify several functionally distinct endothelial cell phenotypes, including an endothelial to mesenchymal transition subtype in adipose tissues. Intercellular communication analysis predicts tissue- and cell type-specific crosstalk between endothelial cells and other cell types through the VEGF, PDGF, TGF-β, and BMP pathways. Regulon analysis of single-cell transcriptome of microglia in pig and 12 other species further identifies MEF2C as an evolutionally conserved regulon in the microglia. Our work describes the landscape of single-cell transcriptomes within diverse pig organs and identifies the heterogeneity of endothelial cells and evolutionally conserved regulon in microglia.
Keyphrases
- single cell
- endothelial cells
- rna seq
- high throughput
- high glucose
- inflammatory response
- gene expression
- genome wide
- vascular endothelial growth factor
- neuropathic pain
- adipose tissue
- transcription factor
- mesenchymal stem cells
- induced apoptosis
- insulin resistance
- metabolic syndrome
- skeletal muscle
- cell therapy
- signaling pathway
- optical coherence tomography
- transforming growth factor
- copy number