Selective migration of neuralized embryonic stem cells to stem cell factor and media conditioned by glioma cell lines

被引:21
作者
Serfozo, Peter [1 ]
Schlarman, Maggie S. [1 ]
Pierret, Chris [1 ]
Maria, Bernard L. [2 ]
Kirk, Mark D. [1 ]
机构
[1] Univ Missouri, Div Biol Sci, Columbia, MO 65211 USA
[2] Med Univ S Carolina, Charles P Darby Childrens Res Inst, Charleston, SC 29425 USA
关键词
Glioma Cell; Neural Stem Cell; Neural Progenitor; Stem Cell Factor; Glioma Cell Line;
D O I
10.1186/1475-2867-6-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Pluripotent mouse embryonic stem (ES) cells can be induced in vitro to become neural progenitors. Upon transplantation, neural progenitors migrate toward areas of damage and inflammation in the CNS. We tested whether undifferentiated and neuralized mouse ES cells migrate toward media conditioned by glioma cell lines (C6, U87 & N1321) or Stem Cell Factor (SCF). Results: Cell migration assays revealed selective migration by neuralized ES cells to conditioned media as well as to synthetic SCF. Migration of undifferentiated ES cells was extensive, but not significantly different from that of controls (Unconditioned Medium). RT-PCR analysis revealed that all the three tumor cell lines tested synthesized SCF and that both undifferentiated and neuralized ES cells expressed c-kit, the receptor for SCF. Conclusion: Our results demonstrate that undifferentiated ES cells are highly mobile and that neural progenitors derived from ES cells are selectively attracted toward factors produced by gliomas. Given that the glioma cell lines synthesize SCF, SCF may be one of several factors that contribute to the selective migration observed.
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页数:8
相关论文
共 41 条
[1]   Migration and differentiation of neural precursor cells can be directed by microglia [J].
Aarum, J ;
Sandberg, K ;
Haeberlein, SLB ;
Persson, MAA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (26) :15983-15988
[2]   Neural stem cells display extensive tropism for pathology in adult brain: Evidence from intracranial gliomas [J].
Aboody, KS ;
Brown, A ;
Rainov, NG ;
Bower, KA ;
Liu, SX ;
Yang, W ;
Small, JE ;
Herrlinger, U ;
Ourednik, V ;
Black, PM ;
Breakefield, XO ;
Snyder, EY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) :12846-12851
[3]   High dose chemotherapy with autologous stem cell rescue in adults with malignant primary brain tumors [J].
Abrey, LE ;
Rosenblum, MK ;
Papadopoulos, E ;
Childs, BH ;
Finlay, JL .
JOURNAL OF NEURO-ONCOLOGY, 1999, 44 (02) :147-153
[4]   Neural precursor cells as carriers for a gene therapeutical approach in tumor therapy [J].
Arnhold, S ;
Hilgers, M ;
Lenartz, D ;
Semkova, I ;
Kochanek, S ;
Voges, J ;
Andressen, C ;
Addicks, K .
CELL TRANSPLANTATION, 2003, 12 (08) :827-837
[5]   EMBRYONIC STEM-CELLS EXPRESS NEURONAL PROPERTIES IN-VITRO [J].
BAIN, G ;
KITCHENS, D ;
YAO, M ;
HUETTNER, JE ;
GOTTLIEB, DI .
DEVELOPMENTAL BIOLOGY, 1995, 168 (02) :342-357
[6]   Gene therapy of experimental brain tumors using neural progenitor cells [J].
Benedetti, S ;
Pirola, B ;
Pollo, B ;
Magrassi, L ;
Bruzzone, MG ;
Rigamonti, D ;
Galli, R ;
Selleri, S ;
Di Meco, F ;
De Fraja, C ;
Vescovi, A ;
Cattaneo, E ;
Finocchiaro, G .
NATURE MEDICINE, 2000, 6 (04) :447-450
[7]   The role of interleukin-8 and its receptors in gliomagenesis and tumoral angiogenesis [J].
Brat, DJ ;
Bellail, AC ;
Van Meir, EG .
NEURO-ONCOLOGY, 2005, 7 (02) :122-133
[8]   Targeted therapy of brain tumors utilizing neural stem and progenitor cells [J].
Burns, MJ ;
Weiss, W .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2003, 8 :E228-E234
[9]   Identification of c-Kit receptor as a regulator of adult neural stem cells in the mammalian eye:: interactions with Notch signaling [J].
Das, AV ;
James, J ;
Zhao, X ;
Rahnenführer, J ;
Ahmad, I .
DEVELOPMENTAL BIOLOGY, 2004, 273 (01) :87-105
[10]  
Ehtesham M, 2002, CANCER RES, V62, P5657