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1.
Dev Comp Immunol ; 114: 103840, 2021 01.
Article in English | MEDLINE | ID: mdl-32858087

ABSTRACT

In the present work we have focused on the Histone Deacetylase (HDAC) control of myeloid cells behavior during Xenopus tail regeneration. Here we show that myeloid differentiation is crucial to modulate the regenerative ability of Xenopus tadpoles in a HDAC activity-dependent fashion. HDAC activity inhibition during the first wave of myeloid differentiation disrupted myeloid cells dynamics in the regenerative bud as well the mRNA expression pattern of myeloid markers, such as LURP, MPOX, Spib and mmp7. We also functionally bridge the spatial and temporal dynamics of lipid droplets, the main platform of lipid mediators synthesis in myeloid cells during the inflammatory response, and the regenerative ability of Xenopus tadpoles. In addition, we showed that 15-LOX activity is necessary during tail regeneration. Taken together our results support a role for the epigenetic control of myeloid behavior during tissue and organ regeneration, which may positively impact translational approaches for regenerative medicine.


Subject(s)
Histone Deacetylases/metabolism , Myeloid Cells/metabolism , Xenopus laevis/physiology , Animals , Biomarkers/metabolism , Cell Differentiation , Cells, Cultured , Epigenesis, Genetic , Gene Expression Regulation, Developmental , Humans , Organogenesis , Regeneration , Regenerative Medicine
3.
Neuroscience ; 423: 206-215, 2019 12 15.
Article in English | MEDLINE | ID: mdl-31682823

ABSTRACT

Trauma to the peripheral nervous system (PNS) results in loss of motor and sensory functions. After an injury, a complex series of events begins, allowing axonal regeneration and target reinnervation. However, this regenerative potential is limited by several factors such as age, distance from the lesion site to the target and severity of lesion. Many studies look for ways to overcome these limitations. Inosine, a purine nucleoside derived from adenosine, emerges as a potential treatment, due to its capacity to regulate axonal growth, neuroprotection and immunomodulation, contributing to motor recovery. However, no studies demonstrated their effects on PNS. C57/Black6 mice were submitted to sciatic nerve crush and received intraperitoneal injections of saline or inosine (70 mg/kg), one hour after injury and daily for one week. To evaluate axonal regeneration and functional recovery, electroneuromyography, Sciatic Function Index (SFI), rotarod and pinprick tests were performed. Our results showed that the inosine group presented a higher number of myelinated fibers and a large amount of fibers within the ideal G-ratio. In addition, the results of electroneuromyography showed greater amplitude of the compound muscle action potentials in the first and second weeks, suggesting anticipation of regeneration in the inosine group. We also observed in the inosine group, motor and sensory neurons survival, reduction in the number of macrophages and myelin ovoids in the sciatic nerves, and an early recovery of motor and sensory functions. Thus, we conclude that the use of inosine accelerates axonal regeneration promoting an early recovery of motor and sensory functions.


Subject(s)
Inosine/pharmacology , Nerve Crush , Nerve Regeneration/drug effects , Peripheral Nerve Injuries/prevention & control , Sciatic Nerve/drug effects , Animals , Electromyography , Injections, Intraperitoneal , Inosine/administration & dosage , Macrophages/drug effects , Macrophages/immunology , Mice , Nerve Regeneration/physiology , Neuroprotective Agents/pharmacology , Peripheral Nerve Injuries/pathology , Recovery of Function/drug effects , Recovery of Function/physiology , Rotarod Performance Test , Sciatic Nerve/injuries
4.
Neuroscience ; 400: 17-32, 2019 02 21.
Article in English | MEDLINE | ID: mdl-30553796

ABSTRACT

Despite advances in technology and rehabilitation, no effective therapies are available for patients with SCI, which remains a major medical challenge. This study compared the efficacy of 3 different doses of mesenchymal stem cells (MSCs) administered by intraperitoneal injection as a therapeutic strategy for compressive SCI. We used adult female C57BL/6 mice that underwent laminectomy at the T9 level, followed by spinal-cord compression for 1 min with a 30-g vascular clip. The animals received an intraperitoneal (i.p.) injection of MSCs (8 × 104, 8 × 105 or 8 × 106 in 500 µl) or DMEM (500 µl), one week after SCI. The cells of the three MSC doses administered i.p. were able to migrate to the injury site, increase local expression of trophic factors, and enhance fiber sparing and/or regeneration, accompanied by substantial improvement in locomotor performance. Cell transplantation at 8 × 105 density showed the best therapeutic potential, leading to significant tissue and functional improvements compared to the other two doses. These findings indicate that i.p. application of MSCs at the density of 8 × 105 yielded the best results, suggesting that this dose is a good choice for SCI treatment.


Subject(s)
Mesenchymal Stem Cell Transplantation/methods , Mesenchymal Stem Cells/physiology , Recovery of Function , Spinal Cord Compression/physiopathology , Spinal Cord Compression/surgery , Animals , Brain-Derived Neurotrophic Factor/metabolism , Female , Gliosis/etiology , Locomotion , Mice, Inbred C57BL , Nerve Fibers, Myelinated/physiology , Neurotrophin 3/metabolism , Spinal Cord Compression/complications
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