Mesenchymal Stem Cells and Pericytes: To What Extent Are They Related?

间充质干细胞 生物 细胞生物学 体内 祖细胞 干细胞 骨髓 周细胞 脂肪组织 干细胞移植修复关节软骨 间充质干细胞的临床应用 病理 免疫学 内皮干细胞 体外 成体干细胞 遗传学 医学 内分泌学
作者
Lucas Eduardo Botelho de Souza,Tathiane M. Malta,Simone Kashima,Dimas Tadeu Covas
出处
期刊:Stem Cells and Development [Mary Ann Liebert]
卷期号:25 (24): 1843-1852 被引量:102
标识
DOI:10.1089/scd.2016.0109
摘要

Mesenchymal stem cells (MSCs) were initially identified as progenitors of skeletal tissues within mammalian bone marrow and cells with similar properties were also obtained from other tissues such as adipose and dental pulp. Although MSCs have been extensively investigated, their native behavior and in vivo identity remain poorly defined. Uncovering the in vivo identity of MSCs has been challenging due to the lack of exclusive cell markers, cellular alterations caused by culture methods, and extensive focus on in vitro properties for characterization. Although MSC site of origin influences their functional properties, these mesenchymal progenitors can be found in the perivascular space in virtually all organs from where they were obtained. However, the precise identity of MSCs within the vascular wall is highly controversial. The recurrent concept that MSCs correspond to pericytes in vivo has been supported mainly by their perivascular localization and expression of some molecular markers. However, this view has been a subject of controversy, in part, due to the application of loose criteria to define pericytes and due to the lack of a marker able to unequivocally identify these cells. Furthermore, recent evidences indicate that subpopulations of MSCs can be found at extravascular sites such as the endosteum. In this opinion review, we bring together the advances and pitfalls on the search for the in vivo identity of MSCs and highlight the recent evidences that suggest that perivascular MSCs are adventitial cells, acting as precursors of pericytes and other stromal cells during tissue homeostasis.
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
1秒前
1秒前
1秒前
2秒前
sxx完成签到,获得积分10
2秒前
2秒前
3秒前
3秒前
are完成签到,获得积分10
4秒前
称心翠容发布了新的文献求助10
4秒前
爆米花应助努力哥采纳,获得30
5秒前
Xing发布了新的文献求助10
5秒前
5秒前
方法和歌完成签到,获得积分10
5秒前
5秒前
6秒前
酷炫葵阴发布了新的文献求助10
6秒前
王坦发布了新的文献求助10
6秒前
jun发布了新的文献求助10
6秒前
7秒前
标致的山水完成签到 ,获得积分10
7秒前
可乐发布了新的文献求助10
7秒前
唐冬灵发布了新的文献求助30
7秒前
zhangyyu关注了科研通微信公众号
7秒前
土豪的帆布鞋完成签到 ,获得积分10
8秒前
陆离发布了新的文献求助80
8秒前
9秒前
adrenline完成签到,获得积分10
10秒前
小桃发布了新的文献求助10
10秒前
JIAYU发布了新的文献求助30
10秒前
力口氵由发布了新的文献求助10
11秒前
飞快的越彬完成签到,获得积分10
11秒前
huangxiaoniu完成签到,获得积分10
11秒前
黄毅发布了新的文献求助10
12秒前
12秒前
12秒前
12秒前
Dusk大寺柯完成签到,获得积分10
13秒前
13秒前
14秒前
高分求助中
Sustainability in Tides Chemistry 2000
Bayesian Models of Cognition:Reverse Engineering the Mind 800
Essentials of thematic analysis 700
A Dissection Guide & Atlas to the Rabbit 600
Very-high-order BVD Schemes Using β-variable THINC Method 568
Внешняя политика КНР: о сущности внешнеполитического курса современного китайского руководства 500
Revolution und Konterrevolution in China [by A. Losowsky] 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 3123185
求助须知:如何正确求助?哪些是违规求助? 2773671
关于积分的说明 7719164
捐赠科研通 2429389
什么是DOI,文献DOI怎么找? 1290277
科研通“疑难数据库(出版商)”最低求助积分说明 621803
版权声明 600251