Mesenchymal stem cells: Cell therapy and regeneration potential

间充质干细胞 再生医学 间充质干细胞的临床应用 干细胞 祖细胞 干细胞移植修复关节软骨 再生(生物学) 生物 CD90型 细胞疗法 免疫学 细胞生物学 多能干细胞 骨髓 成体干细胞 胚胎干细胞 川地34 生物化学 基因
作者
Christina Brown,Christina McKee,Shreeya Bakshi,Keegan Walker,Eryk Hakman,Sophia Halassy,David M. Svinarich,Robert A. Dodds,Chhabi K. Govind,G. Rasul Chaudhry
出处
期刊:Journal of Tissue Engineering and Regenerative Medicine [Wiley]
卷期号:13 (9): 1738-1755 被引量:531
标识
DOI:10.1002/term.2914
摘要

Rapid advances in the isolation of multipotent progenitor cells, routinely called mesenchymal stromal/stem cells (MSCs), from various human tissues and organs have provided impetus to the field of cell therapy and regenerative medicine. The most widely studied sources of MSCs include bone marrow, adipose, muscle, peripheral blood, umbilical cord, placenta, fetal tissue, and amniotic fluid. According to the standard definition of MSCs, these clonal cells adhere to plastic, express cluster of differentiation (CD) markers such as CD73, CD90, and CD105 markers, and can differentiate into adipogenic, chondrogenic, and osteogenic lineages in vitro. However, isolated MSCs have been reported to vary in their potency and self-renewal potential. As a result, the MSCs used for clinical applications often lead to variable or even conflicting results. The lack of uniform characterization methods both in vitro and in vivo also contributes to this confusion. Therefore, the name “MSCs” itself has been increasingly questioned lately. As the use of MSCs is expanding rapidly, there is an increasing need to understand the potential sources and specific potencies of MSCs. This review discusses and compares the characteristics of MSCs and suggests that the variations in their distinctive features are dependent on the source and method of isolation as well as epigenetic changes during maintenance and growth. We also discuss the potential opportunities and challenges of MSC research with the hope to stimulate their use for therapeutic and regenerative medicine.
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
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
zz完成签到,获得积分10
2秒前
cdercder应助小仓采纳,获得10
4秒前
科研通AI6.1应助小仓采纳,获得10
4秒前
Akim应助小仓采纳,获得10
4秒前
科研通AI6.1应助小仓采纳,获得10
5秒前
斯文败类应助小仓采纳,获得10
5秒前
超级小飞侠完成签到 ,获得积分10
5秒前
科研通AI6.2应助小仓采纳,获得10
5秒前
清野应助小仓采纳,获得10
5秒前
yemu3zhi应助小仓采纳,获得10
6秒前
科研通AI6.4应助小仓采纳,获得10
6秒前
Akim应助小仓采纳,获得10
6秒前
9秒前
chenshiyi185发布了新的文献求助10
13秒前
魔幻的雍完成签到,获得积分10
15秒前
落子完成签到 ,获得积分10
16秒前
和谐面包完成签到 ,获得积分10
17秒前
虞夜云完成签到 ,获得积分10
17秒前
17秒前
羊布吃稻完成签到,获得积分10
18秒前
千载完成签到 ,获得积分10
18秒前
酷波er应助LXYang采纳,获得10
21秒前
斯文败类应助安静皓轩采纳,获得10
23秒前
东风应助明理千凝采纳,获得30
23秒前
24秒前
zgx完成签到,获得积分10
26秒前
28秒前
慕青应助chenshiyi185采纳,获得10
28秒前
chy完成签到 ,获得积分10
28秒前
李健的小迷弟应助mxq采纳,获得10
29秒前
HumphreyApplyby完成签到,获得积分10
30秒前
开朗寇发布了新的文献求助20
30秒前
Jerry发布了新的文献求助10
32秒前
35秒前
然然完成签到 ,获得积分10
35秒前
桐桐应助勤奋伟泽采纳,获得10
36秒前
开朗寇完成签到,获得积分10
37秒前
安静皓轩发布了新的文献求助10
38秒前
老王完成签到,获得积分10
38秒前
葳蕤葱茏完成签到 ,获得积分10
40秒前
高分求助中
液晶指向矢仿真分析数据集 8888
Invited Discussant 63O and 64O 1000
Ideology and Meaning-Making under the Putin Regime 750
Advanced Memory Technology 500
Petrology and Plate Tectonics 500
Writing Systems 500
A Handbook of User Experience Research & Design in Libraries 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6864736
求助须知:如何正确求助?哪些是违规求助? 8567424
关于积分的说明 18217094
捐赠科研通 6233579
什么是DOI,文献DOI怎么找? 3048921
关于科研通互助平台的介绍 2050622
邀请新用户注册赠送积分活动 2026676