The Expression of Circ_0000615 in Tenon’s Capsule Fibroblasts and Its Effect on Cell Proliferation and Migration

IF 2.9 4区 医学 Q1 Medicine Journal of biomedical nanotechnology Pub Date : 2023-12-01 DOI:10.1166/jbn.2023.3716
Yanxi Wang, Xing Chen, Zhenhua Yang, Xuelin Yu, Manhua Xu, Gangjing Kang
{"title":"The Expression of Circ_0000615 in Tenon’s Capsule Fibroblasts and Its Effect on Cell Proliferation and Migration","authors":"Yanxi Wang, Xing Chen, Zhenhua Yang, Xuelin Yu, Manhua Xu, Gangjing Kang","doi":"10.1166/jbn.2023.3716","DOIUrl":null,"url":null,"abstract":"To explore the expression of circ_0000615 in HTFs and its effect on cell proliferation and migration. With in vitro culture of HTFs, qRT-PCR was performed to detect the expression of circ_0000615 in HTFs. Cells in logarithmic phase were taken for subsequent experiments, and the\n following groups were constructed, including HTF blank control group (C group); HTFs+10 ng/mL TGF-β1 group (TGF-β1 group); HTFs+si-NC group (si-NC group); and HTFs+si-circ_0000615 group (si-circ_0000615 group). CCK-8 assay was performed to detect cell proliferation,\n Cell Monoclonal Assay was used to detect Cell Monoclonal Formationand, Transwell assay was conducted simultaneously to detect cell migration. According to the results of qRT-PCR, compared with C group, after induction of HTFs with TGF-β1 for 24 h and 48 h, TGF-β1 group\n showed significantly increased expressions of circ_0000615, with statistically significant differences (P < 0.05). After induction of HTFs with TGF-β1, compared with C group, TGF-β1 group had enhanced cell proliferation, monoclonal formation and migration,\n showing statistically significant differences (P < 0.05). Furthermore, after cell transfections for HTFs, compared with si-NC group, si-circ_0000615 group showed obviously downregulated expression of circ_0000615 in HTFs, accompanied by evidently weakened cell proliferation, monoclonal\n formation and migration, statistically significant differences (P < 0.05). Circ_0000615 is highly expressed in HTFs. A silenced expression of circ_0000615 may inhibit the proliferation and migration of HTFs.","PeriodicalId":15260,"journal":{"name":"Journal of biomedical nanotechnology","volume":"22 3","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biomedical nanotechnology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1166/jbn.2023.3716","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

To explore the expression of circ_0000615 in HTFs and its effect on cell proliferation and migration. With in vitro culture of HTFs, qRT-PCR was performed to detect the expression of circ_0000615 in HTFs. Cells in logarithmic phase were taken for subsequent experiments, and the following groups were constructed, including HTF blank control group (C group); HTFs+10 ng/mL TGF-β1 group (TGF-β1 group); HTFs+si-NC group (si-NC group); and HTFs+si-circ_0000615 group (si-circ_0000615 group). CCK-8 assay was performed to detect cell proliferation, Cell Monoclonal Assay was used to detect Cell Monoclonal Formationand, Transwell assay was conducted simultaneously to detect cell migration. According to the results of qRT-PCR, compared with C group, after induction of HTFs with TGF-β1 for 24 h and 48 h, TGF-β1 group showed significantly increased expressions of circ_0000615, with statistically significant differences (P < 0.05). After induction of HTFs with TGF-β1, compared with C group, TGF-β1 group had enhanced cell proliferation, monoclonal formation and migration, showing statistically significant differences (P < 0.05). Furthermore, after cell transfections for HTFs, compared with si-NC group, si-circ_0000615 group showed obviously downregulated expression of circ_0000615 in HTFs, accompanied by evidently weakened cell proliferation, monoclonal formation and migration, statistically significant differences (P < 0.05). Circ_0000615 is highly expressed in HTFs. A silenced expression of circ_0000615 may inhibit the proliferation and migration of HTFs.
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
腱鞘囊成纤维细胞中 Circ_0000615 的表达及其对细胞增殖和迁移的影响
探讨circ_0000615在HTFs中的表达及其对细胞增殖和迁移的影响。体外培养HTFs,采用qRT-PCR检测circ_0000615在HTFs中的表达。取对数期细胞进行后续实验,构建如下组:HTF空白对照组(C组);HTFs+10 ng/mL TGF-β1组(TGF-β1组);HTFs+si-NC组(si-NC组);和html +si-circ_0000615组(si-circ_0000615组)。CCK-8法检测细胞增殖,cell单克隆法检测细胞形成,Transwell法检测细胞迁移。qRT-PCR结果显示,与C组相比,TGF-β1诱导HTFs 24 h和48 h后,TGF-β1组circ_0000615表达显著升高,差异有统计学意义(P < 0.05)。TGF-β1诱导HTFs后,与C组比较,TGF-β1组细胞增殖、单克隆形成和迁移能力增强,差异有统计学意义(P < 0.05)。细胞转染HTFs后,与si-NC组相比,si-circ_0000615组HTFs中circ_0000615的表达明显下调,细胞增殖、单克隆形成和迁移明显减弱,差异有统计学意义(P < 0.05)。Circ_0000615在html中高表达。circ_0000615的沉默表达可能抑制HTFs的增殖和迁移。
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
CiteScore
4.30
自引率
17.20%
发文量
145
审稿时长
2.3 months
期刊介绍: Information not localized
期刊最新文献
Mequinol-Loaded Nano Clay Drug Carriers in a Gelatin Hydrogel for Wound Healing: An Antiinflammatory and Antioxidant Treatment Modality Resveratrol Inhibited Nanoparticles Stromal Interaction Molecule 2 in Regulating miR-20b-5p Signaling Pathway to Improve Mitochondrial Function During Myocardial Ischemia-Reperfusion Injury A Hierarchically Micro- and Nanofibrous Hybrid Hydrogel Derived from Decellularized Skin Matrix with High Bioactivity and Tunable Mechanical Properties for Accelerated Wound Healing Sport Medicine Principles Augment Healing Response in Spinal Cord Injury in a Rat Model Treated with a Curcumin-Loaded Nanocomposite Hydrogel Polyacrylic Acid-Modified Superparamagnetic Iron Oxide Nanoparticles Differentiate Between Hyperplastic and Metastatic Breast Cancer Lymph Nodes
×
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