Identification of human and mouse hematopoietic stem cell populations expressing high levels of mRNA encoding retrovirus receptors

被引:42
作者
Orlic, D
Girard, LJ
Anderson, SM
Pyle, LC
Yoder, MC
Broxmeyer, HE
Bodine, DM
机构
[1] Natl Human Genome Res Inst, Hematopoiesis Sect, Lab Gene Transfer, NIH, Bethesda, MD 20892 USA
[2] James Whitcomb Riley Hosp Children, Dept Pediat, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Microbiol Immunol, Indianapolis, IN 46202 USA
[4] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN 46202 USA
[5] Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
关键词
D O I
10.1182/blood.V91.9.3247.3247_3247_3254
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
One obstacle to retrovirus-mediated gene therapy for human hematopoietic disorders is the low efficiency of gene transfer into pluripotent hematopoietic stem cells (HSC). We have previously shown a direct correlation between retrovirus receptor mRNA levels in mouse HSC and the efficiency with which they are transduced, In the present study, we assayed retrovirus receptor mRNA levels in a variety of mouse and human HSC populations to identify HSC which may be more competent for retrovirus transduction, The highest levels of amphotropic retrovirus receptor (amphoR) mRNA were found in cryopreserved human cord blood HSC, The level of amphoR mRNA in Lin(-)CD34(+)CD38(-) cells isolated from frozen cord blood was 12-fold higher than the level in fresh cord blood Lin(-)CD34(+)CD38(-) cells. In mice, the level of amphoR mRNA in HSC from the bone marrow (BM) of mice treated with stem cell factor and granulocyte-colony stimulating factor was 2.8- to 7.8-fold higher than in HSC from the BM of untreated mice, These findings suggest that HSC from frozen cord blood and cytokine-mobilized BM may be superior targets for amphotropic retrovirus transduction compared with HSC from untreated adult BM, (C) 1998 by The American Society of Hematology.
引用
收藏
页码:3247 / 3254
页数:8
相关论文
共 60 条
[1]   ENVELOPE-BINDING DOMAIN IN THE CATIONIC AMINO-ACID TRANSPORTER DETERMINES THE HOST RANGE OF ECOTROPIC MURINE RETROVIRUSES [J].
ALBRITTON, LM ;
KIM, JW ;
TSENG, L ;
CUNNINGHAM, JM .
JOURNAL OF VIROLOGY, 1993, 67 (04) :2091-2096
[2]   A PUTATIVE MURINE ECOTROPIC RETROVIRUS RECEPTOR GENE ENCODES A MULTIPLE MEMBRANE-SPANNING PROTEIN AND CONFERS SUSCEPTIBILITY TO VIRUS-INFECTION [J].
ALBRITTON, LM ;
TSENG, L ;
SCADDEN, D ;
CUNNINGHAM, JM .
CELL, 1989, 57 (04) :659-666
[3]   PROSPECTS FOR HUMAN-GENE THERAPY [J].
ANDERSON, WF .
SCIENCE, 1984, 226 (4673) :401-409
[4]   EXPRESSION OF HUMAN ADENOSINE-DEAMINASE IN MURINE HEMATOPOIETIC-CELLS [J].
BELMONT, JW ;
MACGREGOR, GR ;
WAGERSMITH, K ;
FLETCHER, FA ;
MOORE, KA ;
HAWKINS, D ;
VILLALON, D ;
CHANG, SMW ;
CASKEY, CT .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (12) :5116-5125
[5]   COMBINATION OF INTERLEUKIN-3 AND INTERLEUKIN-6 PRESERVES STEM-CELL FUNCTION IN CULTURE AND ENHANCES RETROVIRUS-MEDIATED GENE-TRANSFER INTO HEMATOPOIETIC STEM-CELLS [J].
BODINE, DM ;
KARLSSON, S ;
NIENHUIS, AW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8897-8901
[6]  
BODINE DM, 1991, EXP HEMATOL, V19, P206
[7]  
Bodine DM, 1996, BLOOD, V88, P89
[8]  
BODINE DM, 1993, BLOOD, V82, P1975
[9]  
BODINE DM, 1994, BLOOD, V84, P1482
[10]   GENE MARKING TO DETERMINE WHETHER AUTOLOGOUS MARROW INFUSION RESTORES LONG-TERM HEMATOPOIESIS IN CANCER-PATIENTS [J].
BRENNER, MK ;
RILL, DR ;
HOLLADAY, MS ;
HESLOP, HE ;
MOEN, RC ;
BUSCHLE, M ;
KRANCE, RA ;
SANTANA, VM ;
ANDERSON, WF ;
IHLE, JN .
LANCET, 1993, 342 (8880) :1134-1137