Prospective isolation and characterization of mesenchymal stem cells from human placenta using a frizzled-9-specific monoclonal antibody

被引:78
作者
Battula, Venkata Lokesh [1 ]
Treml, Sabrina [1 ]
Abele, Harald [2 ]
Buehring, Hans-Joerg [1 ]
机构
[1] Univ Clin Tubingen, Dept Internal Med 2, Div Hematol Immunol Oncol & Rheumatol, Tubingen, Germany
[2] Univ Clin Tubingen, Dept Obstet & Gynecol, Tubingen, Germany
关键词
placenta; mesenchymal stem cells; multiparameter flow cytometry; frizzled-9;
D O I
10.1111/j.1432-0436.2007.00225.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have recently shown that frizzled-9 (FZD9, CD349) is expressed on the cell surface of cultured mesenchymal stromal cells (MSC) derived from the human bone marrow (BM) and chorionic placenta (PL). To study whether FZD9 is also a marker for naive mesenchymal stem cells (MSC), we analyzed the expression pattern of FZD9 on freshly isolated PL cells and determined the clonogenic potential of isolated FZD9(+) cells using the colony-forming units-fibroblastic (CFU-F) assay. About 0.2% of isolated PL cells were positive for FZD9. Two-color analysis revealed that FZD9(+) PL cells uniformly express CD9, CD63, and CD90, but are heterogeneous for CD10, CD13, and CD26 expression. In contrast to BM-derived MSC, PL-derived MSC expressed only low levels of CD271. Colony assays of sorted cells showed that clonogenic CFU-F reside exclusively in the FZD9(+) but not in the FZD9(-) fraction. Further analysis revealed that CFU-F were enriched by 60-fold in the FZD9(+)CD10(+)CD26(+) fraction but were absent in the FZD9(+)CD10(-)CD26(-) population. Cultured FZD9(+) cells expressed the embryonic stem cell makers Oct-4 and nanog as well as SSEA-4 and TRA1-2-49/6E. In addition, they could be differentiated into functional adipocytes and osteoblasts. This report describes for the first time that FZD9 is a novel and specific marker for the prospective isolation of MSC from human term PL.
引用
收藏
页码:326 / 336
页数:11
相关论文
共 50 条
[1]   Osteogenic differentiation of noncultured immunoisolated bone marrow-derived CD105+ cells [J].
Aslan, Hadi ;
Zilberman, Yoram ;
Kandel, Leonid ;
Liebergall, Meir ;
Oskouian, Rod J. ;
Gazit, Dan ;
Gazit, Zulma .
STEM CELLS, 2006, 24 (07) :1728-1737
[2]   Engraftment and migration of human bone marrow stromal cells implanted in the brains of albino rats - similarities to astrocyte grafts [J].
Azizi, SA ;
Stokes, D ;
Augelli, BJ ;
DiGirolamo, C ;
Prockop, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3908-3913
[3]   Human placenta and bone marrow derived MSC cultured in serum-free, b-FGF-containing medium express cell surface frizzled-9 and SSEA-4 and give rise to multilinelage differentiation [J].
Battula, Venkata Lokesh ;
Bareiss, Petra M. ;
Treml, Sabrina ;
Conrad, Sabine ;
Albert, Ingrid ;
Hojak, Sigrid ;
Abele, Harald ;
Schewe, Bernhard ;
Just, Lothar ;
Skutella, Thomas ;
Buehring, Hans-Jorg .
DIFFERENTIATION, 2007, 75 (04) :279-291
[4]   Bone marrow stromal stem cells: Nature, biology, and potential applications [J].
Bianco, P ;
Riminucci, M ;
Gronthos, S ;
Robey, PG .
STEM CELLS, 2001, 19 (03) :180-192
[5]   Novel markers for the prospective isolation of human MSC [J].
Buehring, Hans-Joerg ;
Battula, Venkata Lokesh ;
Treml, Sabrina ;
Schewe, Bernhard ;
Kanz, Lothar ;
Vogel, Wichard .
HEMATOPOIETIC STEM CELLS VI, 2007, 1106 :262-271
[6]   CDCP1 identifies a broad spectrum of normal and malignant stem/progenitor cell subsets of hematopoietic and nonhematopoietic origin [J].
Bühring, HJ ;
Kuçi, S ;
Conze, T ;
Rathke, G ;
Bartolovic, K ;
Grünebach, F ;
Scherl-Mostageer, M ;
Brümmendorf, TH ;
Schweifer, N ;
Lammers, R .
STEM CELLS, 2004, 22 (03) :334-343
[7]   MESENCHYMAL STEM-CELLS [J].
CAPLAN, AI .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1991, 9 (05) :641-650
[8]   Mesenchymal stem cells: Cell-based reconstructive therapy in orthopedics [J].
Caplan, AI .
TISSUE ENGINEERING, 2005, 11 (7-8) :1198-1211
[9]   Mesenchymal stem cells: Biology and potential clinical uses [J].
Deans, RJ ;
Moseley, AB .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (08) :875-884
[10]   CD164 monoclonal antibodies that block hemopoietic progenitor cell adhesion and proliferation interact with the first mucin domain of the CD164 receptor [J].
Doyonnas, R ;
Chan, JYH ;
Butler, LH ;
Rappold, I ;
Lee-Prudhoe, JE ;
Zannettino, ACW ;
Simmons, PJ ;
Bühring, HJ ;
Levesque, JP ;
Watt, SM .
JOURNAL OF IMMUNOLOGY, 2000, 165 (02) :840-851