Liposomal Nanoparticle-Mediated miR-27b Influences Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells via Peroxisome Proliferator-Activated Receptor Gamma in a Microgravity Environment

Zhiwei He, Yan Zhu, Gentao Fan, H. Qian
{"title":"Liposomal Nanoparticle-Mediated miR-27b Influences Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells via Peroxisome Proliferator-Activated Receptor Gamma in a Microgravity Environment","authors":"Zhiwei He, Yan Zhu, Gentao Fan, H. Qian","doi":"10.1166/NNL.2020.3236","DOIUrl":null,"url":null,"abstract":"This study was aimed at analyzing the effects of liposomal nanoparticle-based miR-27b on PPARγ and osteogenic differentiation of bone marrow mesenchymal stem cells under microgravity. The rat bone marrow mesenchymal stem cells were set as the research object, and the gyroscope\n was employed for simulation of microgravity. The cells were randomized into four groups, including the experimental group A (simulated microgravity+liposomal nanoparticle-mediated miR-27b transfection group), as well as the control groups: group B (simulated microgravity+negative control group),\n group C (simulated microgravity+transfection reagent group) and group D (normal gravity+liposomal nanoparticle-mediatedmiR-27b transfection group). After a two-week osteogenic induction in vitro, staining was performed to assess the lipogenesis rate of the samples. In addition, ALP\n activity and PPARγ mRNA level was detected. The number of alizarin staining-positive osteogenic nodules and ALP activity (0.21±0.44 King unit) in group A was significantly diminished compared to those in group B, C, and D. Moreover, its lipogenesis rate (9.31±1.02%)\n and PPARγ mRNA level (1.86±0.39) were significantly higher than those in group B, C, and D (P < 0.05). The number of alizarin staining-positive osteogenic nodules and ALP activity (0.96±0.18 King unit) in group D were significantly reduced in comparison\n with those in groups B and C, while the lipogenesis rate (4.86±0.77%) and PPARγ mRNA level (0.93±0.34) were significantly higher than those in group B and C (P < 0.05) without difference between group B and group C (P > 0.05). Under a microgravity\n condition, liposomal nanoparticle-mediated miR-27b can impede the differentiation of BMSCs into osteoblasts via regulating PPARγ signal transduction.","PeriodicalId":18871,"journal":{"name":"Nanoscience and Nanotechnology Letters","volume":"12 1","pages":"1301-1308"},"PeriodicalIF":0.0000,"publicationDate":"2020-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanoscience and Nanotechnology Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1166/NNL.2020.3236","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

This study was aimed at analyzing the effects of liposomal nanoparticle-based miR-27b on PPARγ and osteogenic differentiation of bone marrow mesenchymal stem cells under microgravity. The rat bone marrow mesenchymal stem cells were set as the research object, and the gyroscope was employed for simulation of microgravity. The cells were randomized into four groups, including the experimental group A (simulated microgravity+liposomal nanoparticle-mediated miR-27b transfection group), as well as the control groups: group B (simulated microgravity+negative control group), group C (simulated microgravity+transfection reagent group) and group D (normal gravity+liposomal nanoparticle-mediatedmiR-27b transfection group). After a two-week osteogenic induction in vitro, staining was performed to assess the lipogenesis rate of the samples. In addition, ALP activity and PPARγ mRNA level was detected. The number of alizarin staining-positive osteogenic nodules and ALP activity (0.21±0.44 King unit) in group A was significantly diminished compared to those in group B, C, and D. Moreover, its lipogenesis rate (9.31±1.02%) and PPARγ mRNA level (1.86±0.39) were significantly higher than those in group B, C, and D (P < 0.05). The number of alizarin staining-positive osteogenic nodules and ALP activity (0.96±0.18 King unit) in group D were significantly reduced in comparison with those in groups B and C, while the lipogenesis rate (4.86±0.77%) and PPARγ mRNA level (0.93±0.34) were significantly higher than those in group B and C (P < 0.05) without difference between group B and group C (P > 0.05). Under a microgravity condition, liposomal nanoparticle-mediated miR-27b can impede the differentiation of BMSCs into osteoblasts via regulating PPARγ signal transduction.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在微重力环境下,脂质体纳米颗粒介导的miR-27b通过过氧化物酶体增殖物激活受体γ影响骨髓间充质干细胞的成骨分化
本研究旨在分析基于脂质体纳米颗粒的miR-27b对微重力下骨髓间充质干细胞PPARγ和成骨分化的影响。以大鼠骨髓间充质干细胞为研究对象,利用陀螺仪模拟微重力环境。将细胞随机分为实验A组(模拟微重力+脂质体纳米颗粒介导的miR-27b转染组)和对照组:B组(模拟微重力+阴性对照组)、C组(模拟微重力+转染试剂组)和D组(正常重力+脂质体纳米颗粒介导的miR-27b转染组)。体外成骨诱导两周后,染色评估样品的脂肪生成率。同时检测ALP活性和PPARγ mRNA水平。与B、C、D组相比,A组茜素染色阳性的成骨结节数量和ALP活性(0.21±0.44 King unit)均显著降低,脂肪生成率(9.31±1.02%)和PPARγ mRNA水平(1.86±0.39)均显著高于B、C、D组(P < 0.05)。与B、C组相比,D组茜素染色阳性成骨结节数和ALP活性(0.96±0.18 King unit)显著降低,脂肪生成率(4.86±0.77%)和PPARγ mRNA水平(0.93±0.34)显著高于B、C组(P < 0.05), B、C组差异无统计学意义(P < 0.05)。在微重力条件下,脂质体纳米颗粒介导的miR-27b可通过调节PPARγ信号转导阻碍骨髓间充质干细胞向成骨细胞的分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Nanoscience and Nanotechnology Letters
Nanoscience and Nanotechnology Letters Physical, Chemical & Earth Sciences-MATERIALS SCIENCE, MULTIDISCIPLINARY
自引率
0.00%
发文量
0
审稿时长
2.6 months
期刊最新文献
Identification of Immune-Related Prognostic Biomarkers in Pancreatic Cancer Nanocomposite Detection of Elemental Impurities and Process Correlation Analysis of Ceftriaxone Sodium for Injection Astragalus Polysaccharide Nano-Liposomes Modulate the Inflammatory Response and Oxidative Stress in Stroke-Associated Pneumonia by Increasing OIP5-AS1 to Regulate the miR-128-3p/SIRT1 Pathway miR-199a-3p Inhibitor Delivered Through Nano-Drug Delivery Systems Suppresses Tumor Cell Survival and Metastasis Construction of Functional Renal Targeting Nano Drug Liposome and Its Effect on Lupus Nephritis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1