Review Article

Strategies for Regenerating Striatal Neurons in the Adult Brain by Using Endogenous Neural Stem Cells

Table 1

Factors promoting the regeneration of neurons in the striatum. This table lists examples of interventions that could increase the proliferation of neural stem/progenitor cells in the SVZ, enhance the migration of new neurons into the striatum, and promote their differentiation/maturation and survival, which could be promising strategies for replacing degenerated neurons with new ones derived from endogenous neural stem cells of the adult SVZ. SVZ, subventricular zone; RMS, rostral migratory stream; OB, olfactory bulb; TH, tyrosine hydroxylase; EGF, epidermal growth factor; FGF-2, fibroblast growth factor 2; TGF-α, transforming growth factor α; GDNF, glial cell-derived neurotrophic factor; SDF-1α, stromal cell-derived factor 1α; BDNF, brain-derived neurotrophic factor; aCSF artificial cerebrospinal fluid; HI, hypoxic-ischemic cerebral injury; MCAO, middle cerebral artery occlusion; 6-OHDA, 6-hydrodopamine; MPTP, 1-methyl-4-phenyl-1,2,3,6-tetrahydroxydropyridine; hNSCs, human neural stem cells; ESCs, embryonic stem cells.

ProteinModelTechniqueFunction in neurogenesisReferences

EGFIntactInfusion into the lateral ventricle using an osmotic pumpProliferation of SVZ progenitors (18-fold increase compared with saline infusion group)[69]
IntactInfusion into the lateral ventricle using an osmotic pumpProliferation of SVZ progenitors (9.5-fold increase compared with aCSF infusion group)[70]
MCAOOverexpression in the SVZProliferation of SVZ progenitors (1.7-fold increase compared with control vector treatment group)[64]

FGF-2IntactInfusion into the lateral ventricle using an osmotic pumpProliferation of SVZ progenitors (2.4-fold increase compared with serum albumin infusion group)[69]
IntactInfusion into the lateral ventricle using an osmotic pumpProliferation of SVZ progenitors (3.3-fold increase compared with aCSF infusion group)[70]
MCAOInfusion into the cisterna magnaProliferation of SVZ progenitors (increase compared with vehicle treatment group)[65]

Angiopoietin 26-OHDAInfusion into the lateral ventricleProliferation of SVZ progenitors (increase compared with BSA treatment group)[71]

TGF-αIntactInfusion into the lateral ventricle using an osmotic pumpProliferation of SVZ progenitors (14-fold increase compared with albmin infusion group)[69]
6-OHDAInfusion into the striatum using an osmotic pumpProliferation of SVZ progenitors (increase compared with PBS infusion group)[72]
6-OHDAInfusion into the striatum using an osmotic pumpGeneration of neurons in the striatum (immature neuron, increase compared with aCSF infusion group)[73]

GDNFMCAOInfusion into the striatum using an osmotic pumpGeneration of neurons in the striatum (immature neuron, 1.86-fold; mature neuron, 1.2-fold, increase compared with PBS treatment group)[66]

SDF-1αHIMigration of implanted hNSCs toward the injured area in ischemic brain slice (increase)[57]

Tenascin-RIntactTenascin-R expressing cell implantation into the striatumMigration of SVZ new neurons toward the striatum (4-fold increase compared with the Tenascin nonexpression cell implanted group)[74]
Quinolic acidTNR-expressing ESCs implantation into the striatumMigration of SVZ new neurons into the striatum (increase compared with TNR-nonexpression ESCs implanted group)[75]

BDNFIntactInfusion into the lateral ventricle using an osmotic pumpGeneration of neurons in the OB (increase compared with PBS infusion group)[76]
IntactInfusion into the lateral ventricle using an osmotic pumpGeneration of neurons in the striatum (increase compared with PBS infusion group)[77]
R6/2Overexpression in the SVZGeneration of neurons in the striatum (21-fold increase compared with saline group)    [68]