Human Dermis Harbors Distinct Mesenchymal Stromal Cell Subsets

被引:94
作者
Vaculik, Christine [1 ]
Schuster, Christopher [1 ]
Bauer, Wolfgang [1 ]
Iram, Nousheen [1 ]
Pfisterer, Karin [2 ]
Kramer, Gero [3 ]
Reinisch, Andreas [4 ]
Strunk, Dirk [4 ,5 ]
Elbe-Buerger, Adelheid [1 ]
机构
[1] Med Univ Vienna, Div Immunol Allergy & Infect Dis, Dept Dermatol, Lab Cellular & Mol Immunobiol Skin, A-1090 Vienna, Austria
[2] Med Univ Vienna, Mol Immunol Unit, Ctr Pathophysiol Infectiol & Immunol, A-1090 Vienna, Austria
[3] Med Univ Vienna, Dept Urol, A-1090 Vienna, Austria
[4] Med Univ Graz, Stem Cell Res Unit Graz, Graz, Austria
[5] Med Univ Graz, Dept Hematol, Univ Clin Internal Med, Graz, Austria
基金
奥地利科学基金会;
关键词
HUMAN BONE-MARROW; UMBILICAL-CORD BLOOD; KERATINOCYTE STEM/PROGENITOR CELLS; STEM-CELLS; HUMAN PLACENTA; PROGENITOR CELLS; HUMAN SKIN; MULTILINEAGE DIFFERENTIATION; MONOCLONAL-ANTIBODY; CD105(+) CELLS;
D O I
10.1038/jid.2011.355
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Multipotent mesenchymal stromal cells (MSCs) are found in a variety of adult tissues including human dermis. These MSCs are morphologically similar to bone marrow-derived MSCs, but are of unclear phenotype. To shed light on the characteristics of human dermal MSCs, this study was designed to identify and isolate dermal MSCs by a specific marker expression profile, and subsequently rate their mesenchymal differentiation potential. Immunohistochemical staining showed that MSC markers CD73/CD90/CD105, as well as CD271 and SSEA-4, are expressed on dermal cells in situ. Flow cytometric analysis revealed a phenotype similar to bone marrow-derived MSCs. Human dermal cells isolated by plastic adherence had a lower differentiation capacity as compared with bone marrow-derived MSCs. To distinguish dermal MSCs from differentiated fibroblasts, we immunoselected CD271(+) and SSEA-4(+) cells from adherent dermal cells and investigated their mesenchymal differentiation capacity. This revealed that cells with increased adipogenic, osteogenic, and chondrogenic potential were enriched in the dermal CD271(+) population. The differentiation potential of dermal SSEA-4(+) cells, in contrast, appeared to be limited to adipogenesis. These results indicate that specific cell populations with variable mesenchymal differentiation potential can be isolated from human dermis. Moreover, we identified three different subsets of dermal mesenchymal progenitor cells.
引用
收藏
页码:563 / 574
页数:12
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