Department of Oral Medicine, Peking University School and Hospital of Stomatology & National Center of Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Laboratory for Digital and Material Technology of Stomatology & Beijing Key Laboratory of Digital Stomatology & Research Center of Engineering and Technology for Computerized Dentistry Ministry of Health, NMPA Key Laboratory for Dental Materials, Beijing, China.
Department of Oral Medicine, Peking University School and Hospital of Stomatology & National Center of Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Laboratory for Digital and Material Technology of Stomatology & Beijing Key Laboratory of Digital Stomatology & Research Center of Engineering and Technology for Computerized Dentistry Ministry of Health, NMPA Key Laboratory for Dental Materials, Beijing, China; Central Hospital of Shandong First Medical University, Shandong, China.
J Photochem Photobiol B. 2024 Jun;255:112907. doi: 10.1016/j.jphotobiol.2024.112907. Epub 2024 Apr 15.
The objective of this study is to investigate the variances in transcriptome gene expression of normal oral mucosa-derived mesenchymal stem cell (OM-MSC), oral leukoplakia-derived MSC (OLK-MSC) and oral squamous cell carcinoma-derived MSC(OSCC-MSC). as Additionally, the study aims to compare the in vitro proliferation, migration, invasion ability, and response to photodynamic therapy (PDT) of these three MSC, HOK, DOK, leuk1, and Cal27 cell lines.
HOK, DOK, leuk1, Cal27 cells were cultured in vitro. 3 MSC cells were obtained from OM, OLK, OSCC tissue (n = 3) and identified through flow cytometry. They were also cultured in vitro for osteogenic and lipogenic-induced differentiation. Based on the Illumina HiSeq high-throughput sequencing platform, OM-MSC, OLK-MSC, OSCC-MSC (n = 3) were subjected to transcriptome sequencing, functional annotation, and enrichment analysis of differentially expressed genes and related genes. CCK8 assay, wound healing assay, and transwell assay were performed to compare the proliferation, migration, and invasion of the seven types of cells. The 7 cells were incubated with 0, 0.125 mM, 0.25 mM, 0.5 mM, 1 mM, and 2 mM of the photosensitizer (5-aminolevulinic acid, 5-ALA) in vitro. Subsequently, they were irradiated with a 150 mM, 635 nm laser for 1 min, and the cell activity was detected using the CCK8 assay after 24 h. The mitochondrial changes in the 7 cells before and after the treatment of PDT were detected using the JC-10 probe, and the changes in ATP content were measured before and after the PDT treatment.
OM-MSC, OLK-MSC, and OSCC-MSC expressed positive MSC surface markers. After osteogenic and lipogenic-induced differentiation culture, stained calcium nodules and lipid droplets were visible, meeting the identification criteria of MSC. Pathway enrichment analysis revealed that the differentially expressed genes (DEGs) of OSCC-MSC compared to OLK-MSC were primarily associated with the PI3K-Akt signaling pathway and tumor-related pathways. OSCC-MSC exhibited stronger migratory and invasive abilities compared to Cal27. The IC50 values required for OM, OLK, and OSCC-derived MSC were lower than those required for epithelial cells treated with PDT, which were 1.396 mM, 0.9063 mM, and 2.924 mM, respectively. Cell membrane and mitochondrial disruption were observed in seven types of cells after 24 h of PDT treatment. However, HOK, DOK, leuk1, and Cal27 cells had an ATP content increased.
OLK, OSCC epithelial cells require higher concentrations of 5-ALA for PDT treatment than MSC of the same tissue origin. The concentration of 5-ALA required increases with increasing cell malignancy. Differences in the response of epithelial cells and MSC to PDT treatment may have varying impacts on OLK recurrence and malignancy.
本研究旨在探讨正常口腔黏膜来源间充质干细胞(OM-MSC)、口腔白斑病来源间充质干细胞(OLK-MSC)和口腔鳞状细胞癌来源间充质干细胞(OSCC-MSC)的转录组基因表达差异。此外,本研究还旨在比较这三种 MSC(HOK、DOK、leuk1 和 Cal27 细胞系)的体外增殖、迁移、侵袭能力以及对光动力疗法(PDT)的反应。
体外培养 HOK、DOK、leuk1、Cal27 细胞。从 OM、OLK、OSCC 组织中获得 3 个 MSC 细胞(n=3),并通过流式细胞术进行鉴定。还对其进行了成骨和脂肪诱导分化培养。基于 Illumina HiSeq 高通量测序平台,对 OM-MSC、OLK-MSC、OSCC-MSC(n=3)进行转录组测序、功能注释和差异表达基因及相关基因的富集分析。通过 CCK8 检测、划痕愈合实验和 Transwell 实验比较七种细胞的增殖、迁移和侵袭能力。将 7 种细胞在体外分别用 0、0.125 mM、0.25 mM、0.5 mM、1 mM 和 2 mM 的光敏剂(5-氨基酮戊酸,5-ALA)孵育,然后用 150 mM、635 nm 激光照射 1 min,24 h 后用 CCK8 检测细胞活性。用 JC-10 探针检测 7 种细胞在 PDT 治疗前后的线粒体变化,测量 PDT 治疗前后的 ATP 含量。
OM-MSC、OLK-MSC 和 OSCC-MSC 表达阳性 MSC 表面标志物。经成骨和脂肪诱导分化培养后,可见染色钙结节和脂滴,符合 MSC 的鉴定标准。通路富集分析显示,OSCC-MSC 与 OLK-MSC 相比,差异表达基因(DEGs)主要与 PI3K-Akt 信号通路和肿瘤相关通路有关。与 Cal27 相比,OSCC-MSC 具有更强的迁移和侵袭能力。与上皮细胞相比,OM、OLK 和 OSCC 来源的 MSC 所需的 PDT 治疗的 IC50 值更低,分别为 1.396 mM、0.9063 mM 和 2.924 mM。7 种细胞在 PDT 治疗 24 h 后,细胞膜和线粒体均发生破坏。然而,HOK、DOK、leuk1 和 Cal27 细胞的 ATP 含量增加。
OLK、OSCC 上皮细胞进行 PDT 治疗所需的 5-ALA 浓度高于同组织来源的 MSC。所需的 5-ALA 浓度随细胞恶性程度的增加而增加。上皮细胞和 MSC 对 PDT 治疗反应的差异可能对 OLK 复发和恶性程度产生不同的影响。