Mesenchymal stem/progenitor cells developed in cultures from UC blood

被引:215
作者
Yang, SE
Ha, CW
Jung, MH
Jin, HJ
Lee, MK
Song, HS
Choi, SJ
Oh, W
Yang, YS
机构
[1] Medipost Biomed Res Inst, Dept Res & Dev Cellular Therapy, Yongin 449795, Kyungki Do, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Orthoped Surg, Seoul, South Korea
关键词
adipogenic differentiation; chondrogenic differentiation; mesenchymal stem/progenitor cells; osteogenic differentiation; UC blood;
D O I
10.1080/14653240410005041
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background Whether umbilical cord blood (UCB) serves as a source of mesenchymal stem/progenitor cells (MSPC) is controversial. MSPC are the best candidates for cellular therapy of orthopedic skeletal tissues. In order to explore the possibility of UCB as a useful source of MSPC, we identified, expanded in culture, and characterized MSPC from UCB harvests on a large scale. Methods Mononuclear cells isolated from UCB harvests (n = 411) were cultured in media supplemented with 10% FBS. MSPC-like cells cultured from each UCB harvest were expanded ex vivo by successive subcultivation. UCB harvests with a more than 1000-fold expanding capacity ( n = 9) were examined for surface Ag phenotypes and in vitro differentiation potentials into osteogenic, chondrogenic and adipogenic lineages. Results Ninety-five out of a total of 411 UCB units (23.1%) generated MSPC-like cells during cultivation. Nine UCB units (2.2%) yielded MSPC with more than 1000-fold expansion capacity. These cells positively expressed MSPC-related Ag, but did not express myeloid, histocompatibility or endothelial Ag. These cells also possessed multiple capacities for osteogenic, chondrogenic and adipogenic differentiation. Discussion Although the incidence of UCB harvests producing MSPC in culture was low, some of them showed a more than 1000-fold expanding capacity, which is enough in cell numbers to be an allogeneic source for cellular therapy. Our results may encourage the use of UCB as an attractive target for allogeneic cellular therapeutic options in tissue engineering.
引用
收藏
页码:476 / 486
页数:11
相关论文
共 44 条
[31]   Mesenchymal stem cells promote engraftment of human umbilical cord blood-derived CD34+ cells in NOD/SCID mice [J].
Noort, WA ;
Kruisselbrink, AB ;
in't Anker, PS ;
Kruger, M ;
van Bezooijen, RL ;
de Paus, RA ;
Heemskerk, MHM ;
Löwik, CWGM ;
Falkenburg, JHF ;
Willemze, R ;
Fibbe, WE .
EXPERIMENTAL HEMATOLOGY, 2002, 30 (08) :870-878
[32]  
Ohgushi H, 1999, J BIOMED MATER RES, V48, P913, DOI 10.1002/(SICI)1097-4636(1999)48:6<913::AID-JBM22>3.0.CO
[33]  
2-0
[34]   HEMATOPOIESIS - HOW DOES IT HAPPEN [J].
ORKIN, SH .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (06) :870-877
[35]   Multilineage potential of adult human mesenchymal stem cells [J].
Pittenger, MF ;
Mackay, AM ;
Beck, SC ;
Jaiswal, RK ;
Douglas, R ;
Mosca, JD ;
Moorman, MA ;
Simonetti, DW ;
Craig, S ;
Marshak, DR .
SCIENCE, 1999, 284 (5411) :143-147
[36]   Outcomes among 562 recipients of placental-blood transplants from unrelated donors [J].
Rubinstein, P ;
Carrier, C ;
Scaradavou, A ;
Kurtzberg, J ;
Adamson, J ;
Migliaccio, AR ;
Berkowitz, RL ;
Cabbad, M ;
Dobrila, NL ;
Taylor, PE ;
Rosenfield, RE ;
Stevens, CE .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (22) :1565-1577
[37]   In vitro cartilage formation by human adult stem cells from bone marrow stroma defines the sequence of cellular and molecular events during chondrogenesis [J].
Sekiya, I ;
Vuoristo, JT ;
Larson, BL ;
Prockop, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (07) :4397-4402
[38]  
TAVASSOLI M, 1991, P SOC EXP BIOL MED, V196, P367
[39]   Suppression of allogeneic T-cell proliferation by human marrow stromal cells: Implications in transplantation [J].
Tse, WT ;
Pendleton, JD ;
Beyer, WM ;
Egalka, MC ;
Guinan, EC .
TRANSPLANTATION, 2003, 75 (03) :389-397
[40]  
TSUJINO Y, 1993, EXP HEMATOL, V21, P1379