In vivo Tracking of Human Neural Stem Cells Following Transplantation into a Rodent Model of Ischemic Stroke.
- Author:
Da Jeong CHANG
1
;
Hyeyoung MOON
;
Yong Hyun LEE
;
Nayeon LEE
;
Hong J LEE
;
Iksoo JEON
;
Hyunseung LEE
;
Tae Sun HWANG
;
Seung Hun OH
;
Dong Ah SHIN
;
Seung U KIM
;
Kwan Soo HONG
;
Jihwan SONG
Author Information
1. CHA Stem Cell Institute, Department of Biomedical Science, CHA University, Seoul, Korea. jsong@cha.ac.kr
- Publication Type:Original Article
- Keywords:
Human neural stem cells (hNSCs);
Ischemic stroke;
Middle cerebral artery occlusion (MCAo);
Magnetic resonance imaging (MRI);
Feridex;
In vivo tracking
- MeSH:
Brain;
Dextrans;
Humans;
Infarction, Middle Cerebral Artery;
Magnetic Resonance Imaging;
Magnetite Nanoparticles;
Models, Animal;
Neural Stem Cells;
Rodentia;
Stroke;
Track and Field;
Transplants
- From:International Journal of Stem Cells
2012;5(1):79-83
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND AND OBJECTIVES: Ischemic stroke caused by middle cerebral artery occlusion (MCAo) is the major type of stroke, but there are currently very limited options for cure. It has been shown that neural stem cells (NSCs) or neural precursor cells (NPCs) can survive and improve neurological deficits when they are engrafted in animal models of various neurological diseases. However, how the transplanted NSCs or NPCs are act in vivo in the injured or diseased brain is largely unknown. In this study, we utilized magnetic resonance imaging (MRI) techniques in order to understand the fates of human NSCs (HB1.F3) following transplantation into a rodent model of MCAo. METHODS AND RESULTS: HB1.F3 human NSCs were pre-labeled with ferumoxides (Feridex(R))-protamine sulfate complexes, which were visualized and examined by MRI up to 9 weeks after transplantation. Migration of the transplanted cells to the infarct area was further confirmed by histological methods. CONCLUSIONS: Based on these observations, we speculate that the transplanted NSCs have the extensive migratory ability to the injured site, which will in turn contribute to functional recovery in stroke.
