Department of Oral Biology, School of Dental Medicine, State University of New York at Buffalo, Buffalo, NY, USA.
Genomics and Bioinformatics Core, State University of New York at Buffalo, Buffalo, NY, USA.
J Dent Res. 2023 May;102(5):525-535. doi: 10.1177/00220345221147908. Epub 2023 Feb 1.
Saliva-secreting and transporting cells are part of the complex cellular milieu of the human salivary gland, where they play important roles in normal glandular physiology and diseased states. However, comprehensive molecular characterization, particularly at single-cell resolution, is still incomplete, in part due to difficulty in procuring normal human tissues. Here, we perform an in-depth analysis of male and female adult human submandibular gland (SMG) samples by bulk RNA sequencing (RNA-seq) and examine the molecular underpinnings of the heterogeneous cell populations by single-cell (sc) RNA-seq. Our results from scRNA-seq highlight the remarkable diversity of clusters of epithelial and nonepithelial cells that reside in the SMG that is also faithfully recapitulated by deconvolution of the bulk-RNA data sets. Our analyses reveal complex transcriptomic heterogeneity within both the ductal and acinar subpopulations and identify atypical SMG cell types, such as mucoacinar cells that are unique to humans and ionocytes that have been recently described in the mouse. We use CellChat to explore ligand-receptor interactome predictions that likely mediate crucial cell-cell communications between the various cell clusters. Finally, we apply a trajectory inference method to investigate specific cellular branching points and topology that offers insights into the dynamic and complex differentiation process of the adult SMG. The data sets and the analyses herein comprise an extensive wealth of high-resolution information and a valuable resource for a deeper mechanistic understanding of human SMG biology and pathophysiology.
唾液分泌和运输细胞是人类唾液腺复杂细胞环境的一部分,在正常腺体生理学和疾病状态中发挥着重要作用。然而,全面的分子特征描述,特别是单细胞分辨率的描述,仍然不完全,部分原因是难以获得正常的人类组织。在这里,我们通过批量 RNA 测序(RNA-seq)对男性和女性成人下颌下腺(SMG)样本进行了深入分析,并通过单细胞(sc)RNA-seq 检查了异质细胞群体的分子基础。我们的 scRNA-seq 结果突出了存在于 SMG 中的上皮和非上皮细胞簇的显著多样性,这也通过批量 RNA 数据集的去卷积得到了忠实再现。我们的分析揭示了导管和腺泡亚群内复杂的转录组异质性,并鉴定了一些非典型的 SMG 细胞类型,如人类特有的粘液腺细胞和最近在小鼠中描述的离子细胞。我们使用 CellChat 来探索配体-受体相互作用体预测,这些预测可能介导各种细胞簇之间的关键细胞间通讯。最后,我们应用轨迹推断方法来研究特定的细胞分支点和拓扑结构,这为成人 SMG 的动态和复杂分化过程提供了深入的了解。本研究提供了丰富的高分辨率信息数据集和分析,为深入了解人类 SMG 生物学和病理生理学的机制提供了有价值的资源。