| Literature DB >> 28529158 |
Rustem Robertovich Islamov1, Andrey Alexandrovich Izmailov1, Mikhail Evgenyevich Sokolov1, Philip Olegovich Fadeev1, Farid Vagizovich Bashirov1, Anton Alexandrovich Eremeev2, Gulnara Ferdinantovna Shaymardanova1, Maxim Michaylovich Shmarov3, Boris Savelyevich Naroditskiy3, Yuri Alexandrovich Chelyshev1, Igor Aleksandrovich Lavrov4, András Palotás5.
Abstract
Current treatment options for spinal cord injury (SCI) are scarce. One of the most promising innovative approaches include gene-therapy, however no single gene has so far been shown to be of clinical relevance. This study investigates the efficacy of various combinations of vascular endothelial growth factor (VEGF), glial cell-derived neurotrophic factor (GDNF), angiogenin (ANG) and neuronal cell adhesion molecule (NCAM) in rats. Multiple therapeutic genes were administered intrathecally either via adenoviral vectors or by using genetically modified human umbilical cord blood mononuclear cells (hUCBMCs). Following the induction of SCI, serial assessment of cord regeneration was performed, including morphometric analysis of gray and white matters, electrophysiology and behavioral test. The therapeutic gene combinations VEGF+GDNF+NCAM and VEGF+ANG+NCAM had positive outcomes on spinal cord regeneration, with enhanced recovery seen by the cell-based approach when compared to direct gene therapy. The efficacy of the genes and the delivery methods are discussed in this paper, recommending their potential use in SCI.Entities:
Keywords: Adeno-virus; Angiogenin; Glial cell-derived neurotrophic factor; Human umbilical cord blood mononuclear cell; Neural cell adhesion molecule; Spinal cord injury; Vascular endothelial growth factor; Vector
Mesh:
Substances:
Year: 2017 PMID: 28529158 DOI: 10.1016/j.brainresbull.2017.05.005
Source DB: PubMed Journal: Brain Res Bull ISSN: 0361-9230 Impact factor: 4.077