Isolation and characterization of neural stem cells from fetal canine spinal cord

•Spinal cord represents a source of neural stem cells.•These canine neurosphere-shaped have all the morphological aspects compared to other species.•These cells are cryo-resistant and for for further use in clinical trials. Neurogenesis in adult mammals occurs mainly in the subventricular and subgra...

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Veröffentlicht in:Neuroscience letters 2021-11, Vol.765, p.136293-136293, Article 136293
Hauptverfasser: Santos, Sarah Ingrid Pinto, de Oliveira, Vanessa Cristina, Pieri, Naira Caroline Godoy, Bressan, Fabiana Fernandes, Ambrósio, Carlos Eduardo, Feitosa, Matheus Levi Tajra
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container_title Neuroscience letters
container_volume 765
creator Santos, Sarah Ingrid Pinto
de Oliveira, Vanessa Cristina
Pieri, Naira Caroline Godoy
Bressan, Fabiana Fernandes
Ambrósio, Carlos Eduardo
Feitosa, Matheus Levi Tajra
description •Spinal cord represents a source of neural stem cells.•These canine neurosphere-shaped have all the morphological aspects compared to other species.•These cells are cryo-resistant and for for further use in clinical trials. Neurogenesis in adult mammals occurs mainly in the subventricular and subgranular areas of the brain, but there are also reports of its occurrence in the spinal cord. In a study on rats, neural stem cells and neuroprogenitor cells could be obtained through primary spinal cord culture, but there are no studies on these cells in canine species, to date. Dogs represent an appropriate animal model for studies on neurogenesis and neurological disorders. In addition, they are animals of great affective value, and the therapeutic use of neural stem cells can represent a breakthrough in regenerative veterinary medicine. Therefore, this study aimed to determine a protocol for the isolation, culture, and characterization of neural and neuroprogenitor stem cells derived from the spinal cord of canine fetuses. The cells were isolated from spinal cord fragments and cultured in serum-free culture medium supplemented with EGF and FGF-2 growth factors. These cells were observed daily by optical microscopy to analyze their morphological characteristics. From the third day in vitro, it was possible to observe translucent cell groupings, similar to the neurospheres, which approximately ranged from 50 µm to 200 µm at seven days in vitro. Throughout the culture period, the neurospheres developed ribbons in their periphery that migrated and communicated with other neurospheres. RT-PCR revealed that the cells expressed the characteristic genes SOX2, NESTIN, and GFAP. In addition to gene expression, the cells were phenotypically marked in the immunofluorescence assay for the proteins Nestin, GFAP, and β-tubulin III, characterizing them as neurospheres. Our results suggest that the spinal cord may be a source of neural stem cells and neural progenitor cells in canine fetuses. These cells may be an interesting option for neurogenesis and neuroregenerative therapy studies.
doi_str_mv 10.1016/j.neulet.2021.136293
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Neurogenesis in adult mammals occurs mainly in the subventricular and subgranular areas of the brain, but there are also reports of its occurrence in the spinal cord. In a study on rats, neural stem cells and neuroprogenitor cells could be obtained through primary spinal cord culture, but there are no studies on these cells in canine species, to date. Dogs represent an appropriate animal model for studies on neurogenesis and neurological disorders. In addition, they are animals of great affective value, and the therapeutic use of neural stem cells can represent a breakthrough in regenerative veterinary medicine. Therefore, this study aimed to determine a protocol for the isolation, culture, and characterization of neural and neuroprogenitor stem cells derived from the spinal cord of canine fetuses. The cells were isolated from spinal cord fragments and cultured in serum-free culture medium supplemented with EGF and FGF-2 growth factors. These cells were observed daily by optical microscopy to analyze their morphological characteristics. From the third day in vitro, it was possible to observe translucent cell groupings, similar to the neurospheres, which approximately ranged from 50 µm to 200 µm at seven days in vitro. Throughout the culture period, the neurospheres developed ribbons in their periphery that migrated and communicated with other neurospheres. RT-PCR revealed that the cells expressed the characteristic genes SOX2, NESTIN, and GFAP. In addition to gene expression, the cells were phenotypically marked in the immunofluorescence assay for the proteins Nestin, GFAP, and β-tubulin III, characterizing them as neurospheres. Our results suggest that the spinal cord may be a source of neural stem cells and neural progenitor cells in canine fetuses. 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subjects Animals
Canine stem cells
Cell Culture Techniques
Dogs
Fetus
Neural Stem Cells - cytology
Neural stem/progenitor cells
Neurospheres
Spinal Cord - cytology
title Isolation and characterization of neural stem cells from fetal canine spinal cord
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