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Wood, Chelsea R.; Juárez, Esri H.; Ferrini, Francesco; Myint, Peter; Innes, John; Lossi, Laura; Merighi, Adalberto; Johnson, William E.B.
Biochemistry and biophysics reports, 07/2021, Letnik: 26Journal Article
Ex vivo spinal cord slice cultures (SCSC) allow study of spinal cord circuitry, maintaining stimuli responses comparable to live animals. Previously, we have shown that mesenchymal stem/stromal cell (MSC) transplantation in vivo reduced inflammation and increased nerve regeneration but MSC survival was short-lived, highlighting that beneficial action may derive from the secretome. Previous in vitro studies of MSC conditioned medium (CM) have also shown increased neuronal growth. In this study, murine SCSC were cultured in canine MSC CM (harvested from the adipose tissue of excised inguinal fat) and cell phenotypes analysed via immunohistochemistry and confocal microscopy. SCSC in MSC CM displayed enhanced viability after propidium iodide staining. GFAP immunoreactivity was significantly increased in SCSC in MSC CM compared to controls, but with no change in proteoglycan (NG2) immunoreactivity. In contrast, culture in MSC CM significantly decreased the prevalence of βIII-tubulin immunoreactive neurites, whilst Ca2+ transients per cell were significantly increased. These ex vivo results contradict previous in vitro and in vivo reports of how MSC and their secretome may affect the microenvironment of the spinal cord after injury and highlight the importance of a careful comparison of the different experimental conditions used to assess the potential of cell therapies for the treatment of spinal cord injury. •Treatment of spinal slices with conditioned medium caused cell phenotypic changes.•Resident astrocytes become hypertrophic, yet neuronal axonal outgrowth reduced.•Signalling cells reduced in number but increased their signalling activity.•Highlights importance of simulation systems and systemic factors in CNS models.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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