A Spatiotemporal and Machine-Learning Platform Accelerates the Manufacturing of hPSC-derived Esophageal Mucosa.
Ying YangCarmel Grace McCulloughLucas SeningeLihao GuoWoo-Joo KwonYongchun ZhangNancy Yanzhe LiSadhana GaddamCory PanHanson ZhenJessica TorkelsonIan A Glassnull nullGreg CharvilleJianwen QueJoshua M StuartHongxu DingAnthony E OroPublished in: bioRxiv : the preprint server for biology (2023)
Human pluripotent stem cell-derived tissue engineering offers great promise in designer cell-based personalized therapeutics. To harness such potential, a broader approach requires a deeper understanding of tissue-level interactions. We previously developed a manufacturing system for the ectoderm-derived skin epithelium for cell replacement therapy. However, it remains challenging to manufacture the endoderm-derived esophageal epithelium, despite both possessing similar stratified structure. Here we employ single cell and spatial technologies to generate a spatiotemporal multi-omics cell atlas for human esophageal development. We illuminate the cellular diversity, dynamics and signal communications for the developing esophageal epithelium and stroma. Using the machine-learning based Manatee, we prioritize the combinations of candidate human developmental signals for in vitro derivation of esophageal basal cells. Functional validation of the Manatee predictions leads to a clinically-compatible system for manufacturing human esophageal mucosa. Our approach creates a versatile platform to accelerate human tissue manufacturing for future cell replacement therapies to treat human genetic defects and wounds.
Keyphrases
- single cell
- endothelial cells
- machine learning
- induced pluripotent stem cells
- pluripotent stem cells
- rna seq
- cell therapy
- replacement therapy
- stem cells
- gene expression
- artificial intelligence
- deep learning
- genome wide
- bone marrow
- dna methylation
- cell proliferation
- mesenchymal stem cells
- smoking cessation
- copy number
- pi k akt
- wound healing
- cell cycle arrest