2020
DOI: 10.1089/scd.2019.0277
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Identification and Comparison of piRNA Expression Profiles of Exosomes Derived from Human Stem Cells from the Apical Papilla and Bone Marrow Mesenchymal Stem Cells

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Cited by 40 publications
(41 citation statements)
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“…Identification. SCAP-Exo were isolated according to previous protocols [17,18]. For exosome isolation, a conventional culture medium was replaced with a serum-free medium when cells reached 60-80% confluence, and SCAP were cultured for an additional 48 h. Then, the supernatant was centrifuged sequentially at 4°C 3,000 × g for 20 min, 20,000 × g for 30 min, and 120,000 × g for 2 h. Finally, the exosome pellets were resuspended in 200 μL of PBS.…”
Section: Scap-exo Isolation Andmentioning
confidence: 99%
“…Identification. SCAP-Exo were isolated according to previous protocols [17,18]. For exosome isolation, a conventional culture medium was replaced with a serum-free medium when cells reached 60-80% confluence, and SCAP were cultured for an additional 48 h. Then, the supernatant was centrifuged sequentially at 4°C 3,000 × g for 20 min, 20,000 × g for 30 min, and 120,000 × g for 2 h. Finally, the exosome pellets were resuspended in 200 μL of PBS.…”
Section: Scap-exo Isolation Andmentioning
confidence: 99%
“…Importantly, researchers are investigating the most suitable stem cells for specific applications by analyzing their molecular content and phenotypical behavior. Bone marrow mesenchymal stem cells (BMMSCs) and stem cells from the apical papilla (SCAP) of teeth were compared in terms of their piRNAs exosomal cargo content in order to highlight the potential signaling pathways modulated by the secreted vesicles [74]. Previous studies have shown that the exosomes secreted by MSCs exhibit synonymous functions with the cell itself in terms of regeneration, inhibition of inflammation, immunoregulation and tissue repair [75][76][77].…”
Section: Exosomal Loading Of Rare Rnas In Hematological Malignancies mentioning
confidence: 99%
“…hsa-piR-020326, hsa-piR-016735 and hsa-piR-017716 were identified as being highly expressed in SCAP, while hsa-piR-016735 demonstrated high expression in BMMSCs; moreover, 21 miRNAs were identified as being differentially expressed between the exosomes secreted by the two types of cells. Gene enrichment analysis associated the differentially expressed piRNAs with metabolic processes, biological regulation, binding and catalytic activity and cellular processes, all pathways being previously connected with the function of MSCs [74]. The RNA deep sequencing of plasma EVs revealed that indeed the miRNAs are the most abundant RNA species loaded into these vesicles: they constituted 76.20% of mappable reads, followed by piRNA (1.31%), tRNA (1.24%), snRNA (0.18%) and snoRNA (0.01%) [78].…”
Section: Exosomal Loading Of Rare Rnas In Hematological Malignancies mentioning
confidence: 99%
“…As a type of mesenchymal stem cell isolated from early stage tissues during tooth root development, the piRNA expression profiles of SCAPs-derived exosomes was different from BMSCs, including 15 piRNAs that were upregulated, and 6 piRNAs that were downregulated in SCAPs-Exos [ 41 ]. The target genes of the upregulated piRNAs in SCAPs-Exos compared to BMMSC-Exos were significantly enriched in the mitogen-activated protein kinase (MAPK) signaling pathway, which plays an important role in osteogenesis [ 41 ]. However, the specific biological role of piRNAs in osteogenesis, especially the unreported piRNAs (hsa-piR-011273 and hsa-piR-007832), must be further studied.…”
Section: Biological Function Of Exosomes Derived From Oral Tissue Stementioning
confidence: 99%