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1.
Spinal Cord ; 54(5): 347-59, 2016 May.
Article in English | MEDLINE | ID: mdl-26415641

ABSTRACT

STUDY DESIGN: Experimental study. OBJECTIVE: To evaluate the treatment of spinal cord injury with glial cell-derived neurotrophic factor (GDNF) delivered using an adenoviral vector (AdV-GDNF group) in comparison with treatment performed using human umbilical cord blood mononuclear cells (UCB-MCs)-transduced with an adenoviral vector carrying the GDNF gene (UCB-MCs+AdV-GDNF group) in rat. SETTING: Kazan, Russian Federation. METHODS: We examined the efficacy of AdV-GDNF and UCB-MCs+AdV-GDNF therapy by conducting behavioral tests on the animals and morphometric studies on the spinal cord, performing immunofluorescence analyses on glial cells, investigating the survival and migration potential of UCB-MCs, and evaluating the expression of the recombinant GDNF gene. RESULTS: At the 30th postoperative day, equal positive locomotor recovery was observed after both direct and cell-based GDNF therapy. However, after UCB-MCs-mediated GDNF therapy, the area of preserved tissue and the number of spared myelinated fibers were higher than those measured after direct GDNF gene therapy. Moreover, we observed distinct changes in the populations of glial cells; expression patterns of the specific markers for astrocytes (GFAP, S100B and AQP4), oligodendrocytes (PDGFαR and Cx47) and Schwann cells (P0) differed in various areas of the spinal cord of rats treated with AdV-GDNF and UCB-MCs+AdV-GDNF. CONCLUSION: The differences detected in the AdV-GDNF and UCB-MCs+AdV-GDNF groups could be partially explained by the action of UCB-MCs. We discuss the insufficiency and the advantages of these two methods of GDNF gene delivery into the spinal cord after traumatic injury.


Subject(s)
Cell- and Tissue-Based Therapy/methods , Genetic Therapy , Glial Cell Line-Derived Neurotrophic Factor/therapeutic use , Recovery of Function , Spinal Cord Injuries/therapy , Animals , Aquaporin 4/metabolism , Connexins/metabolism , Disease Models, Animal , Female , Gene Transfer Techniques , Genetic Vectors/physiology , Glial Cell Line-Derived Neurotrophic Factor/genetics , Glial Cell Line-Derived Neurotrophic Factor/metabolism , Glial Fibrillary Acidic Protein/metabolism , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , HEK293 Cells , Humans , Locomotion/physiology , Male , Myelin P0 Protein/metabolism , Nerve Tissue Proteins/metabolism , RNA, Messenger/metabolism , Rats , Receptor, Platelet-Derived Growth Factor alpha/metabolism , S100 Calcium Binding Protein beta Subunit/metabolism , Spinal Cord Injuries/genetics , Statistics, Nonparametric
2.
Neuroscience ; 280: 328-39, 2014 Nov 07.
Article in English | MEDLINE | ID: mdl-25218808

ABSTRACT

Exposure to microgravity has been shown to result in damaging alterations to skeletal muscle, bones, and inner organs. In this study, we investigated the effects of microgravity by using a hindlimb unloading model (HUM) in mice. The characteristics of the lumbar spinal cords of HUM mice 30 days after hindlimb unloading were examined. Morphometric analysis showed reductions of the total area, gray matter, and white matter by 17%, 20%, and 12%, respectively. Myelinated fibers in the white matter showed prominent myelin destruction. Analysis of the number of glial fibrillary acidic protein (GFAP+)/S100 calcium-binding protein B (S100B-), GFAP+/S100B+, and GFAP-/S100B+ astrocytes in the ventral horn (VH), central channel area (CC), dorsal root entry zone (DREZ), main corticospinal tract (CST), and ventral funiculi (VF) showed that the number of GFAP+/S100B- astrocytes was increased in the DREZ and CST of HUM mice. Additionally, GFAP+/S100B+ cell numbers were significantly decreased in the VH and CST but did not differ in the CC or DREZ of HUM mice, as compared with the control. The numbers of GFAP-/S100B+ cells were significantly reduced only in the VH of HUM mice. Moreover, the number of ionized calcium-binding adaptor molecule 1 (Iba1+) microglia cells was significantly increased in the CC and DREZ of HUM mice. In control mice, homeobox protein HoxB8 (HoxB8+) cells were found only in the CC; in contrast, HoxB8+ cells were observed in all studied areas in HUM mice, with the greatest number found in the CC. Genome-wide transcriptome analysis of the lumbar spinal cords of HUM mice showed decreased expression of genes encoding myelin, extracellular matrix, cytoskeleton, and cell adhesion proteins. Real-time polymerase chain reaction (PCR) confirmed reductions in the expression of mpz, pmp2, pmp22, and prx genes, which are involved in myelination, as well as decreases in the levels of genes encoding extracellular matrix molecules, including glycoproteins (matrix gla protein (MGP), osteoglycin (OGN), microfibrillar associated protein 5 (MFAP), and collagen, type IV, alpha 1 (COL4A)), proteoglycans (perlecan (heparan sulfate proteoglycan) (HSPG)), and metalloproteinases (lysyl oxidase (LOX)). Thus, our results showed that hindlimb unloading caused decreases in gray and white matter areas, changes in gene expression, alterations in myelination, and phenotypic modifications in glial cells in the lumbar spinal cords of mice.


Subject(s)
Hindlimb Suspension , Neuroglia/metabolism , Spinal Cord/metabolism , Animals , Calcium-Binding Proteins/metabolism , Cell Count , Fluorescent Antibody Technique , Gene Expression Profiling , Glial Fibrillary Acidic Protein , Gray Matter/metabolism , Gray Matter/ultrastructure , Homeodomain Proteins/metabolism , Lumbar Vertebrae , Male , Mice, Inbred C57BL , Microfilament Proteins/metabolism , Microscopy, Electron , Myelin Sheath/metabolism , Myelin Sheath/ultrastructure , Nerve Tissue Proteins/metabolism , Neuroglia/ultrastructure , Real-Time Polymerase Chain Reaction , S100 Calcium Binding Protein beta Subunit/metabolism , Spinal Cord/ultrastructure , White Matter/metabolism , White Matter/ultrastructure
3.
Bull Exp Biol Med ; 154(4): 544-7, 2013 Feb.
Article in English, Russian | MEDLINE | ID: mdl-23486600

ABSTRACT

Using rat model of spinal cord contusion injury at TVIII, we compared the effectiveness of immediate single transplantation of human mononuclear umbilical cord blood cells transfected with pBud-VEGF-FGF2 plasmid and immediate direct injection of the same plasmid into the lesion area. The results suggest that the delivery of therapeutic genes vegf and fgf2 in cells is more effective than direct injection of plasmid DNA with the same genes (judging from the number of myelinated fibers). Better tissue preservation and motor function recovery in experiments with direct injection of plasmid pBud-VEGF-FGF2 suggest that direct gene therapy seems to be an effective additional procedure to the method of gene delivery with transfected stem and progenitor cells.


Subject(s)
Fibroblast Growth Factor 2/metabolism , Genetic Vectors/genetics , Plasmids/genetics , Spinal Cord Injuries/metabolism , Spinal Cord Injuries/therapy , Vascular Endothelial Growth Factor A/metabolism , Animals , Cells, Cultured , Female , Fibroblast Growth Factor 2/genetics , Humans , Male , Rats , Vascular Endothelial Growth Factor A/genetics
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