Comparative study of dedifferentiated fat cell and adipose‐derived stromal cell sheets for periodontal tissue regeneration: In vivo and in vitro evidence

间充质干细胞 间质细胞 脂肪组织 干细胞 再生(生物学) 细胞 牙囊 川地34 细胞生物学 化学 生物 癌症研究 遗传学 内分泌学
作者
Guobin Huang,Bin Xia,Zichao Dai,Rongqiang Yang,Rui Chen,Hefeng Yang
出处
期刊:Journal of Clinical Periodontology [Wiley]
卷期号:49 (12): 1289-1303 被引量:7
标识
DOI:10.1111/jcpe.13705
摘要

Abstract Aim To compare the efficacy of adipocyte‐derived dedifferentiated fat (DFAT) cell and adipose‐derived stromal cell (ADSC) sheets for regenerative treatment of intra‐bony periodontal defects. Materials and Methods DFAT cells were obtained using the ceiling culture method and were compared with ADSCs using Cell Counting Kit‐8, colony formation assay, surface antigen identification, and multilineage differentiation assays. DFAT and ADSC sheets were prepared in a cell sheet culture medium. The biological characteristics of DFAT cell and ADSC sheets were compared using haematoxylin and eosin staining, quantitative reverse transcription polymerase chain reaction, and immunofluorescence staining. Micro‐computed tomography and histological staining were used to compare the effects of the two cell sheets on the repair of periodontal intra‐bony defects in rats. Results DFAT cells and ADSCs demonstrated mesenchymal stem cell characteristics. Both cell types were CD29‐, CD90‐, and CD146‐positive and CD31‐, CD34‐, and CD45‐negative. DFAT cells and ADSCs exhibited similar osteogenic and adipogenic differentiation capabilities and colony formation ability. DFAT cells displayed stronger proliferation capabilities compared with ADSCs. Compared with the ADSC sheets, DFAT cell sheets exhibited a higher expression of periodontal‐related genes and proteins and greater ability to regenerate periodontal tissue. Conclusions Our findings suggest that DFAT cell sheets are an ideal seed cell source and form of cell delivery for periodontal intra‐bony defects.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
大模型应助qian采纳,获得10
刚刚
不配.应助涛1采纳,获得10
1秒前
鸡蛋灌饼完成签到,获得积分10
1秒前
2秒前
顺利的乐枫完成签到 ,获得积分10
2秒前
凯凯搞科研完成签到,获得积分10
2秒前
阿V完成签到,获得积分10
2秒前
典雅的静完成签到,获得积分10
3秒前
BSDL发布了新的文献求助10
3秒前
倩倩完成签到,获得积分10
3秒前
秋水揽星河完成签到,获得积分10
3秒前
岩新完成签到 ,获得积分10
4秒前
xiaogu完成签到,获得积分10
4秒前
Shawn完成签到,获得积分10
4秒前
研途顺利发布了新的文献求助10
5秒前
凯文完成签到,获得积分20
5秒前
gs完成签到,获得积分10
5秒前
dddd完成签到,获得积分10
5秒前
5秒前
科研通AI2S应助yi采纳,获得10
5秒前
ALinaLi完成签到,获得积分10
5秒前
Doinb完成签到,获得积分10
6秒前
六叶草完成签到,获得积分10
6秒前
7秒前
111完成签到,获得积分10
7秒前
萧水白应助zzt采纳,获得10
8秒前
科研通AI2S应助BSDL采纳,获得10
8秒前
DXM完成签到 ,获得积分10
8秒前
Youngen完成签到,获得积分10
9秒前
9秒前
汉堡包应助Robin采纳,获得10
9秒前
cpli完成签到,获得积分10
10秒前
晓伟完成签到,获得积分10
11秒前
科研通AI2S应助ProfWang采纳,获得10
11秒前
Mr.Reese完成签到,获得积分10
11秒前
Yang完成签到,获得积分10
12秒前
科研通AI2S应助茶叶末子采纳,获得10
12秒前
Xiancai完成签到,获得积分10
12秒前
13秒前
chen完成签到,获得积分20
13秒前
高分求助中
Evolution 10000
Sustainability in Tides Chemistry 2800
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
юрские динозавры восточного забайкалья 800
English Wealden Fossils 700
Foreign Policy of the French Second Empire: A Bibliography 500
Chen Hansheng: China’s Last Romantic Revolutionary 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3147003
求助须知:如何正确求助?哪些是违规求助? 2798336
关于积分的说明 7827807
捐赠科研通 2454956
什么是DOI,文献DOI怎么找? 1306492
科研通“疑难数据库(出版商)”最低求助积分说明 627808
版权声明 601565