| Literature DB >> 35948781 |
Siqi Zhang1,2, Yi Sui1, Yifei Zhang1, Shuang Yan1, Chong Ding1, Yanrui Feng1, Jingwei Xiong2, Shicheng Wei3,4.
Abstract
Derivation of salivary gland epithelial progenitors (SGEPs) from human pluripotent stem cells (hPSCs) has great potential in developmental biology and regenerative medicine. At present, no efficient method is available to generate salivary gland cells from hPSCs. Here, we described for the first time a robust protocol for direct differentiation of hPSCs into SGEPs by mimicking retinoic acid and Wnt signaling. These hPSC-derived SGEPs expressed SOX9, KRT5, and KRT19, important progenitor markers of developing salivary glands. CD24 and α-SMA positive cells, capable of restoring the functions of injured salivary glands, were also present in SGEP cultures. Importantly, RNA-sequencing revealed that the SGEPs resembled the transcript profiles of human fetal submandibular glands. Therefore, we provided an efficient protocol to induce hPSCs differentiation into SGEPs. Our study provides a foundation for generating functional hPSCs derived salivary gland acinar cells and three-dimensional organoids, potentially serving as new models for basic study and future translational research.Entities:
Keywords: Differentiation; Human pluripotent stem cells; Progenitors; Protocol; Salivary glands
Year: 2022 PMID: 35948781 DOI: 10.1007/s12015-022-10431-y
Source DB: PubMed Journal: Stem Cell Rev Rep ISSN: 2629-3277 Impact factor: 6.692