GRAFTING OF FAST BLUE LABELED GLIAL-CELLS INTO NEONATAL RAT-BRAIN - DIFFERENTIAL SURVIVAL AND MIGRATION AMONG CELL-TYPES

被引:26
作者
DELOSMONTEROS, AE
BERNARD, R
TILLER, B
ROUGET, P
DEVELLIS, J
机构
[1] UNIV CALIF LOS ANGELES, DEPT PSYCHIAT,MENTAL RETARDAT RES CTR, INST BRAIN RES,RM 68-225 NPI, LOS ANGELES, CA 90024 USA
[2] UNIV CALIF LOS ANGELES, DEPT ANAT & CELL BIOL, LOS ANGELES, CA 90024 USA
[3] UNIV CALIF LOS ANGELES, BIOMED & ENVIRONM SCI LAB, LOS ANGELES, CA 90024 USA
关键词
NEURAL GRAFTS; OLIGODENDROCYTE PROGENITORS; TUMOR FORMATION;
D O I
10.1016/0736-5748(93)90051-E
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cultures of oligodendrocyte progenitor cells, ERD 1.1 cells. a nontransformed immortalized cell line of oligodendrocyte progenitors and C6 glioma cells were labeled with the fluorescent dye Fast Blue and transplanted into brains of 4 day postnatal Wistar rat pups. The localization of fluorescent cells within host brain was examined at various times post-transplantation to determine patterns of cell migration as well as survival and integration among the host tissue. Oligodendrocyte progenitors migrated mainly along white matter tracks, integrating successfully into the host parenchyma. High survival rates were found between 5 and 27 days post grafting. ERD 1.1 cells survived and migrated between 1 and 5 days after transplantation. However, by 27 days survival had dropped from 60 to 20% of the initial cell population. The surviving cells were mainly localized to subventricular and subependymal regions at 27 days. C6 cells migrated extensively rostrally and caudally from the site of injection in the hippocampus and were tumorogenic. This finding confirmed previous reports on the survival and migration patterns of oligodendrocyte progenitors grafted into neonatal brain. However, they show that two cell lines that share phenotypic properties of oligodendrocyte progenitors markedly differ from these cells with respect to migration patterns and integration within host parenchyma. Fast Blue dye was still detectable after repeated cell division in grafted C6 cells, enabling us to track single cells as well as tumor formation. This dye should be useful not only to address issues of development, but also of tumor biology and therapeutic treatment.
引用
收藏
页码:625 / 639
页数:15
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