A single-cell transcriptome atlas of pig skin characterizes anatomical positional heterogeneity.
Qin ZouRong YuanYu ZhangYifei WangTing ZhengRui ShiMei ZhangYujing LiKaixin FeiRan FengBinyun PanXinyue ZhangZhengyin GongLi ZhuGuoqing TangMingzhou LiXuewei LiYanzhi JiangPublished in: eLife (2023)
Different anatomical locations of the body skin show differences in their gene expression patterns depending on different origins, and the inherent heterogeneous information can be maintained in adults. However, highly resolvable cellular specialization is less well characterized in different anatomical regions of the skin. Pig is regarded as an excellent model animal for human skin research in view of its similar physiology to human. In this study, single-cell RNA sequencing was performed on pig skin tissues from six different anatomical regions of Chenghua (CH) pigs, with a superior skin thickness trait, and the back site of large white (LW) pigs. We obtained 233,715 cells, representing seven cell types, among which we primarily characterized the heterogeneity of the top three cell types, including smooth muscle cells (SMCs), endothelial cells (ECs), and fibroblasts (FBs). Then, we further identified several subtypes of SMCs, ECs, and FBs, and discovered the expression patterns of site-specific genes involved in some important pathways such as the immune response and extracellular matrix (ECM) synthesis in different anatomical regions. By comparing differentially expressed genes of skin FBs among different anatomical regions, we considered TNN, COL11A1, and INHBA as candidate genes for facilitating ECM accumulation. These findings of heterogeneity in the main skin cell types from different anatomical sites will contribute to a better understanding of inherent skin information and place the potential focus on skin generation, transmission, and transplantation, paving the foundation for human skin priming.
Keyphrases
- single cell
- rna seq
- soft tissue
- extracellular matrix
- gene expression
- endothelial cells
- wound healing
- high throughput
- immune response
- stem cells
- genome wide
- high glucose
- cell therapy
- risk assessment
- signaling pathway
- induced apoptosis
- optical coherence tomography
- social media
- cell cycle arrest
- cell death
- binding protein
- transcription factor