Analysis and characterization of hematopoietic progenitor cells from fetal bone marrow, adult bone marrow, peripheral blood, and cord blood

被引:28
作者
Wu, AG
Michejda, M
Mazumder, A
Meehan, KR
Menendez, FA
Tchabo, JG
Slack, R
Johnson, MP
Bellanti, JA
机构
[1] Georgetown Univ, Sch Med, Int Ctr Interdisciplinary Stud Immunol, Dept Pediat & Microbiol Immunol, Washington, DC 20007 USA
[2] Georgetown Univ, Sch Med, Bone Marrow Transplant Program, Washington, DC 20007 USA
[3] Georgetown Univ, Sch Med, Dept Lab Med, Washington, DC 20007 USA
[4] Georgetown Univ, Sch Med, Dept Obstet & Gynecol, Washington, DC 20007 USA
[5] Georgetown Univ, Sch Med, Lombardi Canc Ctr, Washington, DC 20007 USA
[6] Wayne State Univ, Hutzel Hosp, Dept Obstet Gynecol, Detroit, MI 48202 USA
关键词
D O I
10.1203/00006450-199908000-00006
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Hematopoietic stem cell transplantation has been increasingly used to replace a defective hematopoietic system and to treat various genetic defects as well as malignant diseases. However, the limitations of conventional bone marrow transplantation have stimulated an intense interest in exploring the use of alternative sources of hematopoietic stem cells, including peripheral blood mononuclear cells (PBMC) and cord blood (CB). ii major investigative effort of our laboratory has been focused on evaluating fetal bone marrow (FBM) for transplantation. The current study compares and characterizes the functional and phenotypic characteristics of FBM, CB, adult bone marrow (ABM), and PBMC by clonogenicity assays, immunogenicity, and the quantification of progenitor cells. There was a striking difference in the proportion of CD34(+) cells in FBM, ABM, PBMC, and CB (24.6%, 2.1%, 0.5%, and 2.0%, respectively). The clonogenic potential, as measured by colony forming unit in culture (CFU-C) assay, was significantly higher in FBM when compared with ABM, PBMC, and CB (202.5, 73.5, 40.8, and 65.5 colonies/10(5) cells, respectively). There was a significant decrease in proliferative responsiveness in mixed lymphocyte reaction (MLR) assay of FBM and CB compared with ABM and PBMC. These observations indicate that each source of hematopoietic stem cells has different intrinsic properties closely correlated with ontogenetic age that is a vital determinant for phenotypic characteristics, lineage commitments, immunogenicity, and proliferative potentials.
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页码:163 / 169
页数:7
相关论文
共 51 条
[1]   FETAL NEURAL GRAFTS AND REPAIR OF THE INJURED SPINAL-CORD [J].
ANDERSON, DK ;
HOWLAND, DR ;
REIER, PJ .
BRAIN PATHOLOGY, 1995, 5 (04) :451-457
[2]  
BATINIC D, 1990, BONE MARROW TRANSPL, V6, P103
[3]   Functional B-cell mass after transplantation of human fetal pancreatic cells - Differentiation or proliferation? [J].
Beattie, GM ;
Otonkoski, T ;
Lopez, AD ;
Hayek, A .
DIABETES, 1997, 46 (02) :244-248
[4]   TRANSPLANTATION OF ALLOGENEIC PERIPHERAL-BLOOD STEM-CELLS MOBILIZED BY RECOMBINANT HUMAN GRANULOCYTE-COLONY-STIMULATING FACTOR [J].
BENSINGER, WI ;
WEAVER, CH ;
APPELBAUM, FR ;
ROWLEY, S ;
DEMIRER, T ;
SANDERS, J ;
STORB, R ;
BUCKNER, CD .
BLOOD, 1995, 85 (06) :1655-1658
[5]   IMPLANTATION OF FETAL TISSUE FOR THE MANAGEMENT OF PARKINSONS-DISEASE - A TECHNICAL NOTE [J].
BREEZE, RE ;
WELLS, TH ;
FREED, CR .
NEUROSURGERY, 1995, 36 (05) :1044-1047
[6]   Detection of maternal DNA in umbilical cord blood by polymerase chain reaction amplification of minisatellite sequences [J].
Briz, M ;
Regidor, C ;
Monteagudo, D ;
Somolinos, N ;
Garaulet, C ;
Forés, R ;
Posada, M ;
Fernández, MN .
BONE MARROW TRANSPLANTATION, 1998, 21 (11) :1097-1099
[7]   HUMAN UMBILICAL-CORD BLOOD AS A POTENTIAL SOURCE OF TRANSPLANTABLE HEMATOPOIETIC STEM PROGENITOR CELLS [J].
BROXMEYER, HE ;
DOUGLAS, GW ;
HANGOC, G ;
COOPER, S ;
BARD, J ;
ENGLISH, D ;
ARNY, M ;
THOMAS, L ;
BOYSE, EA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (10) :3828-3832
[8]   Placental and/or umbilical cord blood: An alternative source of hematopoietic stem cells for transplantation [J].
Cairo, MS ;
Wagner, JE .
BLOOD, 1997, 90 (12) :4665-4678
[9]  
CLEMENT LT, 1990, J IMMUNOL, V145, P102
[10]  
CLEVELAND WW, 1968, LANCET, V2, P1211