2015
DOI: 10.1016/j.neuroscience.2015.07.088
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Tetracycline-regulated expression of OLIG2 gene in human dental pulp stem cells lead to mouse sciatic nerve regeneration upon transplantation

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Cited by 22 publications
(17 citation statements)
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“…They exhibit all the characteristics of MSCs that make them appropriate options for clinical application, being capable of following multi-lineage differentiation, (including neural differentiation [202]) when under suitable culture conditions; presenting self-renewal capacity [203]; expressing MSC phenotypic markers [204], stemness-related markers, cytoskeleton-related markers [205]; and, as expected, not expressing hematopoietic markers (Figure 4b) [203]. Specifically, DPSCs express neural markers [206,207]; produce neurotrophic factors; stimulate the differentiation, growth, and orientation of growing axons; and differentiate into active and functional neurons [208,209]. Compared to other types of MSCs, DPSCs have higher clonogenic capacity, high proliferation, and a larger stem/progenitor cell population.…”
Section: Dental Pulp Mesenchymal Stem Cellsmentioning
confidence: 86%
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“…They exhibit all the characteristics of MSCs that make them appropriate options for clinical application, being capable of following multi-lineage differentiation, (including neural differentiation [202]) when under suitable culture conditions; presenting self-renewal capacity [203]; expressing MSC phenotypic markers [204], stemness-related markers, cytoskeleton-related markers [205]; and, as expected, not expressing hematopoietic markers (Figure 4b) [203]. Specifically, DPSCs express neural markers [206,207]; produce neurotrophic factors; stimulate the differentiation, growth, and orientation of growing axons; and differentiate into active and functional neurons [208,209]. Compared to other types of MSCs, DPSCs have higher clonogenic capacity, high proliferation, and a larger stem/progenitor cell population.…”
Section: Dental Pulp Mesenchymal Stem Cellsmentioning
confidence: 86%
“…Knowing the importance of oligodendrocyte lineage transcription factor 2 in the oligodendrogenic pathway, Askari et al were capable to induce the differentiation of DPSCs into oligodendrocytes by transfection of a tetracycline (Tet)-inducible system expressing oligodendrocyte lineage transcription factor 2 gene. These differentiated cells were then used in the treatment of a local demyelinating lesion of the mouse sciatic nerve by lysolecithin, with observation of repair and regeneration of the injured nerve [209]. The comparative use of DPSCs and neuronal cells originating from the differentiation of DPSCs in the treatment of a 5 mm lesion in the rat sciatic nerve proved that both cell types promoted functional and muscle contraction improvements, associated with the identification of specific markers for angiogenesis, even though no specific differences between the two cell types in promoting nerve regeneration were identified [219].…”
Section: Dental Pulp Mesenchymal Stem Cellsmentioning
confidence: 99%
“…When isolated from patients with neurofibromatosis type 1, DPSCs have a proliferation rate higher than that of normal cells; thus, DPSCs represent a suitable model for neurofibromatosis type 1 [ 72 ]. Moreover, DPSC-derived oligoprogenitor cells showed high therapeutic potential in an animal model of sciatic nerve injury [ 73 ], indicating its potential as a therapeutic for amelioration of myelin injuries in the PNS [ 74 ]. When SHED-CM was investigated for peripheral nerve regeneration, SHED-CM-treated Schwann cells exhibited a significantly increased number of neuronal and angiogenesis related genes.…”
Section: Dscs and Neurodegenerative Disordersmentioning
confidence: 99%
“…The conditioned medium of SHED containing the factors involved in multiple neuro-regenerative mechanisms might account for the results. Iran scientists also showed that improvement of behavioral symptoms was efficiently observed in the mouse model of local sciatic demyelination damage by lysolecithin after transplantation of the DPSCs, to which a tetracycline (Tet)-inducible system expressing OLIG2 gene had been transfected (Askari et al, 2015). And Maraldi et al confirmed strong potential of bioengineered constructs of stem cell (including dental pulp derived stem cell)-collagen scaffold for correcting large cranial defects in a rat model and highlighting the role of stem cells in neovascularization during skeletal defect reconstruction (Maraldi et al, 2013).…”
Section: Application Of Oral Derived Stem Cells In Non-oral Diseasesmentioning
confidence: 99%