Targeted migration and differentiation of engrafted neural precursor cells in amyloid beta-treated hippocampus in rats.
- Author:
Jun TANG
1
;
Hai-Wei XU
;
Xiao-Tang FAN
;
Zhi-Fang LI
;
Da-Bing LI
;
Li YANG
;
Guang-Ji ZHOU
Author Information
- Publication Type:Journal Article
- MeSH: Amyloid beta-Peptides; administration & dosage; metabolism; Animals; Cell Differentiation; Cell Movement; Embryonic Stem Cells; cytology; physiology; transplantation; Fluorescent Antibody Technique; Glial Fibrillary Acidic Protein; metabolism; Green Fluorescent Proteins; metabolism; Hippocampus; cytology; physiology; Injections, Intraventricular; Male; Neurons; cytology; physiology; transplantation; Rats; Rats, Wistar; Stem Cell Transplantation
- From: Neuroscience Bulletin 2007;23(5):263-270
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo observe the migration and differentiation of the neural precursor cells (NPCs) that derived from murine embryonic stem cells (ESCs) when they were transplanted into amyloid beta (A beta)-treated rat hippocampus.
METHODSMESPU35, a murine ESC cell line that express the enhanced green fluorescent protein (EGFP), was induced differentiation into nestin-positive NPCs by modified serum-free methods. The A beta plaques and the differentiation of the grafted cells were observed by immunofluorescent staining.
RESULTSComparing 16 weeks with 4 weeks post-transplantation, the migration distance increased about 5 times; the rate of migratory NPCs differentiating into glial fibrillary acidic protein (GFAP)-positive cells kept rising from (30.41+/-1.45) % to (49.25+/-1.23) %, and the rate of NPCs differentiating into neurofilament 200 (NF200) positive cells increased from (16.68+/-0.95) % to (27.94+/-1.21) %. Meanwhile, the GFAP-positive cells targeting to the ipsilateral side of A beta plaques increased from 60.2% to 81.3%, while the NF200-positive cells increased from 61.3% to 84.1%. The migration distance had significant positive linear correlations to the neuronal differentiation rate (r = 0.991) and to the astrocytic differentiation rate (r = 0.953).
CONCLUSIONEngrafted NPCs migrate targetedly to the A beta injection site and differentiate into neurons and astrocytes.