Human Neural Stem Cells Transplantation in Experimental Intracerebral Hemorrhage.
- Author:
Sang Wuk JEONG
1
;
Kon CHU
;
Keun Hwa JUNG
;
Seung U KIM
;
Man Ho KIM
;
Jae Kyu ROH
Author Information
1. Brain Disease Research Center, Ajou University, Korea.
- Publication Type:Original Article
- Keywords:
Intracerebral hemorrhage;
Neural stem cell;
Neural transplantation;
Immunohistochemistry
- MeSH:
Adult;
Animals;
Astrocytes;
Brain;
Cerebral Hemorrhage*;
Collagenases;
Craniocerebral Trauma;
Extremities;
Humans*;
Immunohistochemistry;
Neural Stem Cells*;
Neuroglia;
Neurons;
Rats;
Rotarod Performance Test;
Stem Cell Transplantation;
Stroke;
Transplants
- From:Journal of the Korean Neurological Association
2003;21(2):183-190
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Intracerebral hemorrhage (ICH) is associated with a considerable proportion of stroke and head injuries, but except for supportive care, there is no medical therapy available. Transplantation of human neural stem cells (NSCs) can be used to reduce behavioral deficit in experimental ischemic infarct model. However, effect of stem cell transplantation in experimental intracerebral hemorrhage (ICH) is unknown. We hypothesized that NSCs could migrate and differentiate into neurons or glial cells, and improve functional outcome in ICH. METHODS: Experimental ICH was made by intrastriatal administration of bacterial collagenase in adult rats. Animals were randomized to receive intravenously either immortalized Lac-Z positive human NSCs (5x1 06 in 500microL, n=15) or same volume of saline (n=12) on the following day. Animals were evaluated for 8 weeks after surgery with behavioral test battery. After 8 weeks, animals were sacrificed and the brains were sectioned. Transplanted NSCs were detected by X-gal histochemistry or beta-gal immunohistochemistry, and differentiation of grafted NSCs were evaluated by double labeling of GFAP, NeuN, or neurofilament. RESULTS: Transplanted NSCs migrated to the side of peri-hematomal areas, and differentiated into neurons and astrocytes. NSCs injection group showed improved performances on rotarod test after 2 weeks and on limb placing test after 5 weeks compared with control group (p<0.05) and these effect persisted up to 8 weeks. CONCLUSIONS: Intravenously injected NSCs enter rat brain with ICH, and differentiate into astrocytes or neuronal cell, which lead to functional recovery. These findings show the possibility that NSCs can be used to reduce neurological deficits in the experimental ICH.
