Avabhrath Nagashree, Foltz Lauren, Grimes Mark
Division of Biological Sciences, Center for Biomolecular Structure and Dynamics, and Center for Structural and Functional Neuroscience, The University of Montana, Missoula, MT 59812, USA.
Division of Biological Sciences, Center for Biomolecular Structure and Dynamics, and Center for Structural and Functional Neuroscience, The University of Montana, Missoula, MT 59812, USA.
STAR Protoc. 2025 Mar 21;6(1):103532. doi: 10.1016/j.xpro.2024.103532. Epub 2024 Dec 20.
Here, we present a protocol to generate craniofacial cartilage organoids from human stem cells via neural crest stem cells (NCSCs). We describe steps for inducing human embryonic stem cells (hESCs) or induced pluripotent stem cells (iPSCs) to form NCSCs using sequential treatments of small molecules and growth factors and isolating NCSCs by magnetic bead sorting. We then detail procedures for defining conditions where NCSCs migrate together and self-organize into craniofacial cartilage organoids. Recapitulating craniofacial chondrogenesis will facilitate craniofacial reconstruction and disease modeling. For complete details on the use and execution of this protocol, please refer to Foltz et al..
在此,我们展示了一种通过神经嵴干细胞(NCSCs)从人类干细胞生成颅面软骨类器官的方案。我们描述了使用小分子和生长因子的序贯处理诱导人类胚胎干细胞(hESCs)或诱导多能干细胞(iPSCs)形成NCSCs,并通过磁珠分选分离NCSCs的步骤。然后,我们详细说明了确定NCSCs一起迁移并自组织成颅面软骨类器官的条件的程序。重现颅面软骨形成将有助于颅面重建和疾病建模。有关本方案使用和执行的完整详细信息,请参考福尔茨等人的研究。