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Transgenic human embryonic stem cells overexpressing FGF2 stimulate neuroprotection following spinal cord ventral root avulsion
MR. Araújo, S. Kyrylenko, AB. Spejo, MV. Castro, RS. Ferreira Junior, B. Barraviera, ALR. Oliveira,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
- MeSH
- doxycyklin terapeutické užití MeSH
- fibrinová tkáňová adheziva toxicita MeSH
- fibroblastový růstový faktor 2 genetika metabolismus MeSH
- genetické vektory fyziologie MeSH
- krysa rodu rattus MeSH
- lidé MeSH
- lidské embryonální kmenové buňky metabolismus transplantace MeSH
- míšní kořeny patologie MeSH
- modely nemocí na zvířatech MeSH
- motorické neurony metabolismus patologie MeSH
- neuroglie účinky léků metabolismus MeSH
- pohyb buněk MeSH
- potkani inbrední LEW MeSH
- proteiny nervové tkáně metabolismus MeSH
- radikulopatie chemicky indukované chirurgie MeSH
- regulace genové exprese účinky léků genetika MeSH
- tkáňová adheziva toxicita MeSH
- viabilita buněk účinky léků genetika MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- lidé MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Ventral root avulsion (VRA) triggers a strong glial reaction which contributes to neuronal loss, as well as to synaptic detachment. To overcome the degenerative effects of VRA, treatments with neurotrophic factors and stem cells have been proposed. Thus, we investigated neuroprotection elicited by human embryonic stem cells (hESC), modified to overexpress a human fibroblast growth factor 2 (FGF-2), on motoneurons subjected to VRA. Lewis rats were submitted to VRA (L4-L6) and hESC/FGF-2 were applied to the injury site using a fibrin scaffold. The spinal cords were processed to evaluate neuronal survival, synaptic stability, and glial reactivity two weeks post lesion. Then, qRT-PCR was used to assess gene expression of β2-microglobulin (β2m), TNFα, IL1β, IL6 and IL10 in the spinal cord in vivo and FGF2 mRNA levels in hESC in vitro. The results indicate that hESC overexpressing FGF2 significantly rescued avulsed motoneurons, preserving synaptic covering and reducing astroglial reactivity. The cells were also shown to express BDNF and GDNF at the site of injury. Additionally, engraftment of hESC led to a significant reduction in mRNA levels of TNFα at the spinal cord ventral horn, indicating their immunomodulatory properties. Overall, the present data suggest that hESC overexpressing FGF2 are neuroprotective and can shift gene expression towards an anti-inflammatory environment.
Center for the Study of Venoms and Venomous Animals São Paulo State Brazil
Department of Biology Faculty of Medicine Masaryk University Brno Czech Republic
Citace poskytuje Crossref.org
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- $a Araújo, Marta Rocha $u Department of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, Sao Paulo, Brazil. $7 gn_A_00008041
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- $a Ventral root avulsion (VRA) triggers a strong glial reaction which contributes to neuronal loss, as well as to synaptic detachment. To overcome the degenerative effects of VRA, treatments with neurotrophic factors and stem cells have been proposed. Thus, we investigated neuroprotection elicited by human embryonic stem cells (hESC), modified to overexpress a human fibroblast growth factor 2 (FGF-2), on motoneurons subjected to VRA. Lewis rats were submitted to VRA (L4-L6) and hESC/FGF-2 were applied to the injury site using a fibrin scaffold. The spinal cords were processed to evaluate neuronal survival, synaptic stability, and glial reactivity two weeks post lesion. Then, qRT-PCR was used to assess gene expression of β2-microglobulin (β2m), TNFα, IL1β, IL6 and IL10 in the spinal cord in vivo and FGF2 mRNA levels in hESC in vitro. The results indicate that hESC overexpressing FGF2 significantly rescued avulsed motoneurons, preserving synaptic covering and reducing astroglial reactivity. The cells were also shown to express BDNF and GDNF at the site of injury. Additionally, engraftment of hESC led to a significant reduction in mRNA levels of TNFα at the spinal cord ventral horn, indicating their immunomodulatory properties. Overall, the present data suggest that hESC overexpressing FGF2 are neuroprotective and can shift gene expression towards an anti-inflammatory environment.
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- $a Kyrylenko, Sergiy $u Department of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, Sao Paulo, Brazil; Department of Biology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
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- $a Barraviera, Benedito $u Department of Tropical Diseases, Botucatu Medical School, São Paulo State University (UNESP-Univ. Estadual Paulista), São Paulo State, Brazil; Center for the Study of Venoms and Venomous Animals (CEVAP), São Paulo State University (UNESP-Univ. Estadual Paulista), São Paulo State, Brazil.
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- $a Oliveira, Alexandre Leite Rodrigues $u Department of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, Sao Paulo, Brazil. Electronic address: alroliv@unicamp.br.
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