PMID- 37516879 OWN - NLM STAT- MEDLINE DCOM- 20230731 LR - 20230801 IS - 1749-799X (Electronic) IS - 1749-799X (Linking) VI - 18 IP - 1 DP - 2023 Jul 29 TI - Exosomes promote hFOB1.19 proliferation and differentiation via LINC00520. PG - 546 LID - 10.1186/s13018-023-04021-y [doi] LID - 546 AB - BACKGROUND: Osteoporosis remains a significant clinical challenge worldwide. Recent studies have shown that exosomes stimulate bone regeneration. Thus, it is worthwhile to explore whether exosomes could be a useful therapeutic strategy for osteoporosis. The purpose of this study was to investigate the effects of exosomes derived from human umbilical cord mesenchymal stem cells (hucMSCs) on osteoblast proliferation and differentiation. METHODS: Exosomes were isolated from hucMSCs. Bioinformatics analysis was performed to identify the differentially expressed lncRNAs in myeloma-derived mesenchymal stem cells. Plasmids encoding LINC00520 or short hairpin RNA of LINC00520 were transfected into hucMSCs and then exosomes were isolated. After human osteoblasts hFOB1.19 were exposed to the obtained exosomes, cell survival, cell cycle, apoptosis and calcium deposits of hFOB1.19 cell were detected by MTT, 7-aminoactinomycin D, Annexin V-FITC/propidium iodide and Alizarin red staining, respectively. RESULTS: In hFOB1.19 cells, 10 x 10(9)/mL hucMSC-derived exosomes inhibited cell proliferation, arrested cell cycle, and promoted apoptosis, while hucMSCs or 1 x 10(9)/mL exosomes promoted cell proliferation, accelerated cell cycle, and promoted calcium deposits and the expression of OCN, RUNX2, collagen I and ALP. In hFOB1.19 cells, exosomes from hucMSCs with LINC00520 knockdown reduced the survival and calcium deposits, arrested the cell cycle, and enhanced the apoptosis, while exosomes from hucMSCs overexpressing LINC00520 enhance the proliferation and calcium deposits and accelerated the cell cycle. CONCLUSIONS: LINC00520 functions as a modulator of calcium deposits, and exosomes derived from hucMSCs overexpressing LINC00520 might be a novel therapeutic approach for osteoporosis. CI - (c) 2023. The Author(s). FAU - Wu, Jin AU - Wu J AD - Medical School of Chinese PLA, Chinese PLA General Hospital, No. 28 Fuxing Road, Haidian District, Beijing, 100853, China. AD - Department of Orthopedics, National Clinical Research Center for Orthopedics, Sports Medicine and Rehabilitation, Chinese PLA General Hospital, Beijing, 100853, China. AD - Department of Orthopedics, The 909th Hospital, School of Medicine, Xiamen University, Zhangzhou, 363000, China. FAU - Zhang, Licheng AU - Zhang L AD - Medical School of Chinese PLA, Chinese PLA General Hospital, No. 28 Fuxing Road, Haidian District, Beijing, 100853, China. zhanglcheng218@126.com. AD - Department of Orthopedics, National Clinical Research Center for Orthopedics, Sports Medicine and Rehabilitation, Chinese PLA General Hospital, Beijing, 100853, China. zhanglcheng218@126.com. FAU - Liu, Hui AU - Liu H AD - Department of Orthopedics, The 909th Hospital, School of Medicine, Xiamen University, Zhangzhou, 363000, China. FAU - Zhang, Jinhui AU - Zhang J AD - Department of Orthopedics, The 909th Hospital, School of Medicine, Xiamen University, Zhangzhou, 363000, China. FAU - Tang, Peifu AU - Tang P AD - Medical School of Chinese PLA, Chinese PLA General Hospital, No. 28 Fuxing Road, Haidian District, Beijing, 100853, China. pftang301@163.com. AD - Department of Orthopedics, National Clinical Research Center for Orthopedics, Sports Medicine and Rehabilitation, Chinese PLA General Hospital, Beijing, 100853, China. pftang301@163.com. LA - eng PT - Journal Article DEP - 20230729 PL - England TA - J Orthop Surg Res JT - Journal of orthopaedic surgery and research JID - 101265112 RN - SY7Q814VUP (Calcium) SB - IM MH - Humans MH - *Calcium MH - *Exosomes/genetics MH - Cell Cycle/genetics MH - Cell Differentiation/genetics MH - Cell Proliferation/genetics PMC - PMC10387216 OTO - NOTNLM OT - Human umbilical cord mesenchymal stem cell-derived exosomes OT - LINC00520 OT - Osteoblast OT - Osteoporosis COIS- No competing interests were involved in this study. EDAT- 2023/07/30 01:06 MHDA- 2023/07/31 11:42 PMCR- 2023/07/29 CRDT- 2023/07/29 23:27 PHST- 2023/01/13 00:00 [received] PHST- 2023/07/15 00:00 [accepted] PHST- 2023/07/31 11:42 [medline] PHST- 2023/07/30 01:06 [pubmed] PHST- 2023/07/29 23:27 [entrez] PHST- 2023/07/29 00:00 [pmc-release] AID - 10.1186/s13018-023-04021-y [pii] AID - 4021 [pii] AID - 10.1186/s13018-023-04021-y [doi] PST - epublish SO - J Orthop Surg Res. 2023 Jul 29;18(1):546. doi: 10.1186/s13018-023-04021-y.