A novel role for proliferin-2 in the ex vivo expansion of hematopoietic stem cells

被引:19
作者
Choong, ML
Tan, MCL
Luo, B
Lodish, HF
机构
[1] Ctr Bioproc Technol, Singapore 117597, Singapore
[2] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02139 USA
关键词
hematopoietic progenitor cell; stromal cell; bone marrow; fetal liver; in vitro expansion;
D O I
10.1016/S0014-5793(03)00844-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A family of proliferin genes was discovered on a microarray analysis of hematopoiesis supportive stromal cell lines. Proliferin-2 (PLF2) increased the frequency of long-term culture-initiating cells (LTC-IC) from 1 in 340 to 1 in 256 of the primary hematopoietic stem cell (HSC)-enriched bone marrow cells grown on MS5.1 feeder layer. A repeat using AFT024 feeder layer also showed a similar increase in LTG-IC (from 1 in 386 cells to 1 in 260 cells). The clonogenic output of the LTC-ICs was also increased significantly. The growth of various hematopoietic and stromal cell lines treated with PLF2 was found to increase by 4-27%, as measured by cell count and DNA synthesis assay. These findings open up the possibility of using PLF2 as a new member of the growth factor cocktails for the ex vivo expansion of HSC. (C) 2003 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:155 / 162
页数:8
相关论文
共 39 条
[21]   Impaired steel factor responsiveness differentially affects the detection and long-term maintenance of fetal liver hematopoietic stem cells in vivo [J].
Miller, CL ;
Rebel, VI ;
Helgason, CD ;
Lansdorp, PM ;
Eaves, CJ .
BLOOD, 1997, 89 (04) :1214-1223
[22]   Regulatory mechanisms in stem cell biology [J].
Morrison, SJ ;
Shah, NM ;
Anderson, DJ .
CELL, 1997, 88 (03) :287-298
[23]   CHARACTERIZATION OF THE MITOGEN-REGULATED PROTEIN (PROLIFERIN) RECEPTOR [J].
NELSON, JT ;
ROSENZWEIG, N ;
NILSENHAMILTON, M .
ENDOCRINOLOGY, 1995, 136 (01) :283-288
[24]   RELATIONSHIP BETWEEN MITOGEN-REGULATED PROTEIN (MRP) AND PROLIFERIN (PLF), A MEMBER OF THE PROLACTIN GROWTH-HORMONE FAMILY [J].
NILSENHAMILTON, M ;
HAMILTON, RT ;
ALVAREZAZAUSTRE, E .
GENE, 1987, 51 (2-3) :163-170
[25]   Mitomycin C as an alternative to irradiation to inhibit the feeder layer growth in long-term culture assays [J].
Ponchio, L ;
Duma, L ;
Oliviero, B ;
Gibelli, N ;
Pedrazzoli, P ;
della Cuna, GR .
CYTOTHERAPY, 2000, 2 (04) :281-286
[26]   Factor(s) secreted by AFT024 fetal liver cells following stimulation with human cytokines are important for human LTC-IC growth [J].
Punzel, M ;
Gupta, P ;
Roodell, M ;
Mortari, F ;
Verfaillie, CM .
LEUKEMIA, 1999, 13 (07) :1079-1084
[27]   ISOLATION AND CHARACTERIZATION OF SOMATOLACTIN, A NEW-PROTEIN RELATED TO GROWTH-HORMONE AND PROLACTIN FROM ATLANTIC COD (GADUS-MORHUA) PITUITARY-GLANDS [J].
RANDWEAVER, M ;
NOSO, T ;
MURAMOTO, K ;
KAWAUCHI, H .
BIOCHEMISTRY, 1991, 30 (06) :1509-1515
[28]   Pitfalls in the use of several ''housekeeping'' genes as standards for quantitation of mRNA: The example of thyroid cells [J].
Savonet, V ;
Maenhaut, C ;
Miot, F ;
Pirson, I .
ANALYTICAL BIOCHEMISTRY, 1997, 247 (01) :165-167
[29]   STK-1, THE HUMAN HOMOLOG OF FLK-2/FLT-3, IS SELECTIVELY EXPRESSED IN CD34(+) HUMAN BONE-MARROW CELLS AND IS INVOLVED IN THE PROLIFERATION OF EARLY PROGENITOR STEM-CELLS [J].
SMALL, D ;
LEVENSTEIN, M ;
KIM, E ;
CAROW, C ;
AMIN, S ;
ROCKWELL, P ;
WITTE, L ;
BURROW, C ;
RATAJCZAK, MZ ;
GEWIRTZ, AM ;
CIVIN, CI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :459-463
[30]   EVALUATION OF QUANTITATIVE VARIATION IN GENE-EXPRESSION [J].
SPANAKIS, E ;
BROUTYBOYE, D .
NUCLEIC ACIDS RESEARCH, 1994, 22 (05) :799-806