微泡
小桶
牙周膜干细胞
细胞生物学
小RNA
生物
外体
间充质干细胞
化学
细胞分化
信号转导
碱性磷酸酶
基因表达
转录组
基因
遗传学
生物化学
酶
作者
Liangkun Xie,Jianzhong Chen,Xiaobin Ren,Mingzhu Zhang,Nattawut Thuaksuban,Thongchai Nuntanaranont,Zheng Guan
标识
DOI:10.1016/j.archoralbio.2020.104984
摘要
This study investigated circRNA and lncRNA expression profile in exosomes derived from periodontal ligament stem cell (PDLSC) before and after its osteogenic differentiation. Exosomes derived from PDLSCs before (EX0) and after osteogenic induction for 5 (EX5) and 7 (EX7) days were harvested and exosomal circRNAs and lncRNAs were analyzed by RNA sequencing. Certain RNAs showing significantly altered expression were selected for qRT-PCR verification. The circRNA–miRNA–mRNA network and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed. All groups of exosomes showed typical characteristics under nanoparticle tracking analysis, flow cytometry assay and transmission electron microscopy. 69–557 circRNAs and 2907–11581 lncRNAs were found in EX0, EX5 and EX7, which were broadly distributed across the 24 pairs of human chromosomes. Compared with EX0, 3 circRNAs and 2 lncRNAs were up-regulated and 39 circRNAs and 5 lncRNAs down-regulated consistently through out of EX5 and EX7, p < 0.05. qRT-PCR confirmed certain those consistently expressed RNAs, such as circ lysophosphatidic acid receptor 1 (LPAR1). KEGG analysis showed that those consistent expressed RNAs closely related to TGF-beta pathway, MAPK pathway, mTOR pathway and FoxO signaling pathways regulating pluripotency of stem cells. Exosomal circRNAs and lncRNAs had significant expression changes during the early phase of osteogenic differentiation of PDLSCs. Further study would be taken for understanding the roles of exosomal circRNAs and lncRNAs playing in osteogenic differentiation of PDLSCs.
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