Research Center for Tissue Repair and Regeneration affiliated to the Medical Innovation Research Department, Chinese PLA General Hospital, 28 Fu Xing Road, 100048, Beijing, P. R. China.
PLA Key Laboratory of Tissue Repair and Regenerative Medicine, Beijing Key Research Laboratory of Skin Injury, Repair and Regeneration, Chinese PLA General Hospital and PLA Medical College, 28 Fu Xing Road, 100048, Beijing, P.R. China.
J Mol Histol. 2022 Oct;53(5):857-867. doi: 10.1007/s10735-022-10098-2. Epub 2022 Aug 25.
Eccrine sweat gland (SG) restrictedly exists in mouse foot pads indicating that mouse plantar dermis (PD) contains the SG lineage-restricted niches. However, it is still unclear how these niches can affect stem cell fate towards SG. In this study, we tried to find the key cues by which stem cells sense and interact with the SG lineage-specific niches both in vivo and in vitro. Firstly, we used transcriptomics RNA sequencing analysis to screen differentially expressed genes between SG cells and epidermal stem cells (ES), and used proteomic analysis to screen differentially expressed proteins between PD and dorsal dermis (DD). Notch1 was found differentially expressed in both gene and protein levels, and was closely related to SG morphogenesis based on Gene Ontology (GO) enrichment analysis. Secondly, the spatial-temporal changes of Notch1 during embryonic and post-natal development of SG were detected. Thirdly, mouse mesenchymal stem cells (MSCs) were introduced into SG-like cells in vitro in order to further verify the possible roles of Notch1. Results revealed that Notch1 was continuously down-regulated along with the process of SG morphogenesis in vivo, and also along with the process that MSCs differentiated into SG-like cells in vitro. Hence, we suggest that Notch1 possibly acts as with roles of "gatekeeper" during SG development and regulates the interactions between stem cells and the SG lineage-specific niches. This study might help for understanding mechanisms of embryonic SG organogenesis.
汗腺(SG)仅存在于小鼠的脚掌垫中,这表明小鼠足底真皮(PD)中含有 SG 谱系受限的小生境。然而,这些小生境如何影响干细胞向 SG 的命运仍然不清楚。在这项研究中,我们试图通过体内和体外实验来寻找干细胞感知和与 SG 谱系特异性小生境相互作用的关键线索。首先,我们使用转录组学 RNA 测序分析筛选 SG 细胞与表皮干细胞(ES)之间差异表达的基因,并使用蛋白质组学分析筛选 PD 与背皮(DD)之间差异表达的蛋白质。Notch1 在基因和蛋白水平上均有差异表达,基于基因本体论(GO)富集分析,Notch1 与 SG 形态发生密切相关。其次,检测了 Notch1 在 SG 胚胎和出生后发育过程中的时空变化。第三,将小鼠间充质干细胞(MSCs)引入体外 SG 样细胞中,以进一步验证 Notch1 的可能作用。结果表明,Notch1 在体内 SG 形态发生过程中持续下调,在 MSCs 体外分化为 SG 样细胞的过程中也持续下调。因此,我们认为 Notch1 可能在 SG 发育过程中充当“守门员”的角色,调节干细胞与 SG 谱系特异性小生境之间的相互作用。本研究有助于理解胚胎 SG 器官发生的机制。