Concise Review: The Surface Markers and Identity of Human Mesenchymal Stem Cells

被引:766
作者
Lv, Feng-Juan [1 ,2 ,3 ]
Tuan, Rocky S. [4 ]
Cheung, Kenneth M. C. [1 ,2 ,3 ]
Leung, Victor Y. L. [1 ,2 ,3 ]
机构
[1] Univ Hong Kong, Dept Orthopaed & Traumatol, Li Ka Shing Fac Med, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Stem Cell & Regenerat Med Consortium, Li Ka Shing Fac Med, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Ctr Reprod Dev & Growth, Li Ka Shing Fac Med, Hong Kong, Hong Kong, Peoples R China
[4] Univ Pittsburgh, Sch Med, Dept Orthopaed Surg, Ctr Cellular & Mol Engn, Pittsburgh, PA 15261 USA
基金
美国国家科学基金会;
关键词
Mesenchymal stem cells; Surface epitopes; CD271; CD146; Markers; Pericytes; Niche; Regenerative medicine; HUMAN BONE-MARROW; UMBILICAL-CORD BLOOD; MULTIPOTENT STROMAL CELLS; NEURAL GANGLIOSIDE GD2; IN-VITRO; ADIPOSE-TISSUE; HUMAN PLACENTA; STEM/PROGENITOR CELLS; MONOCLONAL-ANTIBODY; EXPRESSION PROFILE;
D O I
10.1002/stem.1681
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The concept of mesenchymal stem cells (MSCs) is becoming increasingly obscure due to the recent findings of heterogeneous populations with different levels of stemness within MSCs isolated by traditional plastic adherence. MSCs were originally identified in bone marrow and later detected in many other tissues. Currently, no cloning based on single surface marker is capable of isolating cells that satisfy the minimal criteria of MSCs from various tissue environments. Markers that associate with the stemness of MSCs await to be elucidated. A number of candidate MSC surface markers or markers possibly related to their stemness have been brought forward so far, including Stro-1, SSEA-4, CD271, and CD146, yet there is a large difference in their expression in various sources of MSCs. The exact identity of MSCs in vivo is not yet clear, although reports have suggested they may have a fibroblastic or pericytic origin. In this review, we revisit the reported expression of surface molecules in MSCs from various sources, aiming to assess their potential as MSC markers and define the critical panel for future investigation. We also discuss the relationship of MSCs to fibroblasts and pericytes in an attempt to shed light on their identity in vivo.
引用
收藏
页码:1408 / 1419
页数:12
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