成骨细胞
破骨细胞
细胞生物学
化学
骨吸收
细胞分化
吸收
骨髓
外体
内分泌学
生物
免疫学
微泡
生物化学
体外
小RNA
基因
作者
Yu-Seong Park,Hyun‐Woo Kim,Jin-Hyeon Hwang,Jung‐Young Eom,Dong-Ha Kim,Jinho Park,Hyun‐Jin Tae,Seunghoon Lee,Jae Gyu Yoo,Jee‐In Kim,Jae‐Hwan Lim,In‐Sook Kwun,Moon‐Chang Baek,Young‐Eun Cho,Do‐Kyun Kim
出处
期刊:Nutrients
[Multidisciplinary Digital Publishing Institute]
日期:2023-04-27
卷期号:15 (9): 2107-2107
被引量:11
摘要
Osteoblasts and osteoclasts play crucial roles in bone formation and bone resorption. We found that plum-derived exosome-like nanovesicles (PENVs) suppressed osteoclast activation and modulated osteoblast differentiation. PENVs increased the proliferation, differentiation, and mineralization of osteoblastic MC3T3-E1 cells and osteoblasts from mouse bone marrow cultures. Notably, PENVs elevated the expression of osteoblastic transcription factors and osteoblast differentiation marker proteins in MC3T3-E1 cells. Higher levels of phosphorylated BMP-2, p38, JNK, and smad1 proteins were detected in PENV-treated MC3T3-E1 cells. Additionally, the number of TRAP-positive cells was significantly decreased in PENV-treated osteoclasts isolated from osteoblasts from mouse bone marrow cultures. Importantly, osteoclastogenesis of marker proteins such as PPAR-gamma, NFATc1, and c-Fos were suppressed by treatment with PENVs (50 μg/mL). Taken together, these results demonstrate that PENVs can be used as therapeutic targets for treating bone-related diseases by improving osteoblast differentiation and inhibiting osteoclast activation for the first time.
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