Zhang Siqi, Sui Yi, Zhang Yifei, Yan Shuang, Ding Chong, Feng Yanrui, Xiong Jingwei, Wei Shicheng
Central Laboratory, and Department of Oral and Maxillofacial Surgery School and Hospital of Stomatology, Peking University, Beijing, 100081, China.
Institute of Molecular Medicine, Peking University, Beijing, 100871, China.
Stem Cell Rev Rep. 2023 Feb;19(2):430-442. doi: 10.1007/s12015-022-10431-y. Epub 2022 Aug 10.
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.
从人多能干细胞(hPSC)中衍生唾液腺上皮祖细胞(SGEP)在发育生物学和再生医学中具有巨大潜力。目前,尚无有效的方法从hPSC中生成唾液腺细胞。在此,我们首次描述了一种通过模拟视黄酸和Wnt信号通路将hPSC直接分化为SGEP的可靠方案。这些源自hPSC的SGEP表达SOX9、KRT5和KRT19,这些是发育中唾液腺的重要祖细胞标志物。SGEP培养物中也存在能够恢复受损唾液腺功能的CD24和α-SMA阳性细胞。重要的是,RNA测序显示SGEP类似于人类胎儿下颌下腺的转录谱。因此,我们提供了一种诱导hPSC分化为SGEP的有效方案。我们的研究为生成功能性hPSC衍生的唾液腺腺泡细胞和三维类器官奠定了基础,有可能作为基础研究和未来转化研究的新模型。