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单细胞 RNA 测序揭示了 PDGFRα+基质细胞亚群,这些细胞亚群在胚胎唾液腺类器官中促进前腺泡细胞分化。

Single-cell RNA sequencing reveals PDGFRα+ stromal cell subpopulations that promote proacinar cell differentiation in embryonic salivary gland organoids.

机构信息

Department of Biological Sciences, University at Albany, State University of New York, Albany, NY 12222, USA.

Graduate Program in Molecular, Cellular, Developmental and Neural Biology, University at Albany, State University of New York, Albany, NY 12222, USA.

出版信息

Development. 2022 Mar 15;149(6). doi: 10.1242/dev.200167. Epub 2022 Mar 25.

Abstract

Stromal cells can direct the differentiation of epithelial progenitor cells during organ development. Fibroblast growth factor (FGF) signaling is essential for submandibular salivary gland development. Through stromal fibroblast cells, FGF2 can indirectly regulate proacinar cell differentiation in organoids, but the mechanisms are not understood. We performed single-cell RNA-sequencing and identified multiple stromal cell subsets, including Pdgfra+ stromal subsets expressing both Fgf2 and Fgf10. When combined with epithelial progenitor cells in organoids, magnetic-activated cell-sorted PDGFRα+ cells promoted proacinar cell differentiation similarly to total stroma. Gene expression analysis revealed that FGF2 increased the expression of multiple stromal genes, including Bmp2 and Bmp7. Both BMP2 and BMP7 synergized with FGF2, stimulating proacinar cell differentiation but not branching. However, stromal cells grown without FGF2 did not support proacinar organoid differentiation and instead differentiated into myofibroblasts. In organoids, TGFβ1 treatment stimulated myofibroblast differentiation and inhibited the proacinar cell differentiation of epithelial progenitor cells. Conversely, FGF2 reversed the effects of TGFβ1. We also demonstrated that adult salivary stromal cells were FGF2 responsive and could promote proacinar cell differentiation. These FGF2 signaling pathways may have applications in future regenerative therapies.

摘要

基质细胞可以在器官发育过程中指导上皮祖细胞的分化。成纤维细胞生长因子(FGF)信号对于下颌下唾液腺的发育至关重要。通过基质成纤维细胞,FGF2 可以间接调节类器官中前腺泡细胞的分化,但机制尚不清楚。我们进行了单细胞 RNA 测序,鉴定出多种基质细胞亚群,包括同时表达 Fgf2 和 Fgf10 的 Pdgfra+基质亚群。当与类器官中的上皮祖细胞结合时,经过磁激活细胞分选的 PDGFRα+细胞与总基质相似,促进前腺泡细胞的分化。基因表达分析显示,FGF2 增加了多个基质基因的表达,包括 Bmp2 和 Bmp7。BMP2 和 BMP7 与 FGF2 协同作用,刺激前腺泡细胞分化而不刺激分支。然而,在没有 FGF2 的情况下生长的基质细胞不能支持前腺泡类器官的分化,而是分化为肌成纤维细胞。在类器官中,TGFβ1 处理刺激肌成纤维细胞分化并抑制上皮祖细胞的前腺泡细胞分化。相反,FGF2 逆转了 TGFβ1 的作用。我们还证明了成年唾液腺基质细胞对 FGF2 有反应,并能促进前腺泡细胞的分化。这些 FGF2 信号通路可能在未来的再生治疗中有应用。

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