Gene transfection mediated by polyethyleneimine-polyethylene glycol nanocarrier prevents cisplatin-induced spiral ganglion cell damage

Autor: Guan-gui Chen, Min Mao, Li-zi Qiu, Qi-ming Liu
Jazyk: angličtina
Rok vydání: 2015
Předmět:
tamoxifen
Src kinase
PP2
trauma
regeneration
neuroprotection
auranofin
dextromethorphan
rosiglitazone
Alzheimer′s disease
neuroinflammation
neurodegeneration
microglia
astrocytes
nerve regeneration
spinal cord
electroacupuncture therapy
neural stem cells
notch signaling pathway
inflammation
survival curve
proliferation
differentiation
real-time quantitative PCR
western blot assay
neural regeneration
superparamagnetic iron oxide
magnetic guidance
bone marrow mesenchymal stem cells
spinal cord injury
cell transplantation
magnetic resonance image
lumbar puncture
spinal cord transection
average combined score
magnetic resonance imaging
diffusion tensor imaging
fractional anisotropy
apparent diffusion coefficient
fiber tractography
peripheral nerve injury
sciatic nerve
hypothermia
blood-nerve barrier
Evans blue tracer
neural degeneration
polyethyleneimine-polyethylene glycol
spiral ganglion cells
X-linked inhibitor of apoptosis protein
gene therapy
nanocarrier
cisplatin
ototoxicity
cochlea
Neurology. Diseases of the nervous system
RC346-429
Zdroj: Neural Regeneration Research, Vol 10, Iss 3, Pp 425-431 (2015)
Druh dokumentu: article
ISSN: 1673-5374
DOI: 10.4103/1673-5374.153691
Popis: Polyethyleneimine-polyethylene glycol (PEI-PEG), a novel nanocarrier, has been used for transfection and gene therapy in a variety of cells. In our previous study, we successfully carried out PEI-PEG-mediated gene transfer in spiral ganglion cells. It remains unclear whether PEI-PEG could be used for gene therapy with X-linked inhibitor of apoptosis protein (XIAP) in the inner ear. In the present study, we performed PEI-PEG-mediated XIAP gene transfection in the cochlea of Sprague-Dawley rats, via scala tympani fenestration, before daily cisplatin injections. Auditory brainstem reflex tests demonstrated the protective effects of XIAP gene therapy on auditory function. Immunohistochemical staining revealed XIAP protein expression in the cytoplasm of cells in the spiral ganglion, the organ of Corti and the stria vascularis. Reverse transcription-PCR detected high levels of XIAP mRNA expression in the cochlea. The present findings suggest that PEI-PEG nanocarrier-mediated XIAP gene transfection results in XIAP expression in the cochlea, prevents damage to cochlear spiral ganglion cells, and protects hearing.
Databáze: Directory of Open Access Journals