School of Medicine, Huaqiao University, Quanzhou, Fujian 362021, China; Stem Cell Laboratory, The Second Affiliated Hospital of Fujian Medical University, China.
School of Medicine, Huaqiao University, Quanzhou, Fujian 362021, China.
Gene. 2021 Apr 5;775:145447. doi: 10.1016/j.gene.2021.145447. Epub 2021 Jan 19.
Limbal stem cells (LSCs) reside in the basal layer of limbal epithelial cells (LECs). They are crucial for maintenance of corneal epithelium homeostasis and corneal wound healing. Their stemness is determined by their gene expression pattern. Despite of several positive identifiers have been reported, the unique biomarker for LSCs still remain elusive. Differentially expressed genes (DEGs) between stem cells and differentiated cells affect the fate of stem cells via specific signaling pathway. In order to understand the DEGs in the LSCs, RNA-seq was firstly conducted using a mouse model. A total of 1907 up-regulated DEGs and 395 down-regulated DEGs were identified in the limbus (L) compared to central cornea (CC) and conjunctiva (Cj). Reliability of the expression of genes from RNA-seq analysis was evaluated by quantitative real-time polymerase chain reaction (qRT-PCR) and immunofluorescence staining. The expression pattern of putative biomarkers was considered to be age-related. In up-regulated DEGs GO analysis, 570 gene ontology (GO) terms were significantly enriched. Five groups of genes related with biological processes from these significantly enriched GO terms comprised ionic transport, regulation of tissue development, muscle contraction, visual perception, and cell adhesion, which were clustered as a weighted similar network. Whereas, in down-regulated DEGs GO analysis, 61 GO terms were significantly enriched and only one group of ATP biosynthesis and metabolic process were clustered. Furthermore, we identified 55 signaling pathways by the Kyoto Encyclopedia of Genes and Genomes (KEGG) database based on up-regulated genes and 14 KEGG pathways based on down-regulated genes. In this study, we provide a landscape of the expression of putative LSCs biomarkers and stemness-related signaling pathways in a mouse model. Our findings could aid in the identification of LSC niche factors that may be related to the stemness of the LSCs.
角膜缘干细胞 (LSCs) 位于角膜缘上皮细胞 (LECs) 的基底层。它们对于维持角膜上皮细胞稳态和角膜伤口愈合至关重要。它们的干性由其基因表达模式决定。尽管已经报道了几种阳性标志物,但 LSCs 的独特标志物仍然难以捉摸。干细胞和分化细胞之间差异表达的基因 (DEGs) 通过特定的信号通路影响干细胞的命运。为了了解 LSCs 中的 DEGs,首先使用小鼠模型进行了 RNA-seq 分析。与中央角膜 (CC) 和结膜 (Cj) 相比,在角膜缘 (L) 中总共鉴定出 1907 个上调的 DEGs 和 395 个下调的 DEGs。通过定量实时聚合酶链反应 (qRT-PCR) 和免疫荧光染色评估 RNA-seq 分析中基因表达的可靠性。基因表达模式被认为与年龄相关。在上调的 DEGs GO 分析中,570 个基因本体 (GO) 术语显著富集。从这些显著富集的 GO 术语中,与生物学过程相关的 5 组基因包括离子转运、组织发育调节、肌肉收缩、视觉感知和细胞黏附,它们被聚类为加权相似网络。相比之下,在下调的 DEGs GO 分析中,61 个 GO 术语显著富集,只有一组与 ATP 生物合成和代谢过程相关的基因被聚类。此外,我们根据上调基因确定了 55 个信号通路,根据下调基因确定了 14 个京都基因与基因组百科全书 (KEGG) 数据库的信号通路。在这项研究中,我们提供了一个小鼠模型中 LSCs 潜在标志物和干性相关信号通路表达的图谱。我们的研究结果可能有助于确定与 LSCs 干性相关的 LSC 生态位因素。