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. 2015 Jan 26;7(1):126–136. doi: 10.4252/wjsc.v7.i1.126

Table 2.

Preclinical results of adult neural stem cells against neurodegenerative diseases

Targeted disease animal model Cell source Injection method Result Animal species Ref.
Demyelinated spinal cord injury Frontal cortex, temporal cortex, hippocampus, and subventricular/subependymal zone of frontal lobe The midline of the dorsal columns of the spinal cord at three longitudinal sites The cells elicited extensive remyelination with a peripheral myelin pattern similar to Schwanncell myelination The remyelinated axons conducted impulses at near normal conduction velocities Rat [56]
Multiple sclerosis (lysolecithin-demyelinated brain) Temporal lobe Local injection to demyelinated brain regions Transplanted cells migrated to lesions without extending into normal white matter. Implanted progenitors matured as oligodendrocytes, and developed myelin-associated antigens Rat [57]
Global brain ischemia Temporal lobe The posterior periventricular region above the hippocampus Adult human NPCs survived, migrated into ischemic regions, and differentiated into functional neural cells No information about therapeutic effects Rat [58]
Global brain ischemia Temporal lobe Left hippocampus After in vitro differentiation Injected cells migrated preferentially into an ischemic lesion, which was mediated by SDF-1α and CXCR4 signaling pathways No information about therapeutic effects Rat [59]
Focal ischemic stroke Temporal lobe Contralateral lateral ventricle Transplanted cells reduced infarction volumes and enhanced motor activity Rat [18]