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Background: The regeneration of the peripheral nerves after injuries is still a challenging fundamental and clinical problem. The cell therapy and nerve guide conduit construction are promising modern approaches. Nowadays, different sources of cells for transplantation are available. But it is little known about the interaction between fetal central nervous system cells and peripheral nerve tissue. In this study, we analyzed the development of the fetal neocortex and spinal cord solid grafts injected into the gelatin hydrogel conduits and their effects on sciatic nerve regeneration after cut injury.
Methods: Frontal neocortex tissue was obtained from E19.5 and spinal cord tissue was obtained from E14.5 fetuses harvested from transgenic EGFP mice. The grafts were injected into the hydrogel conduits which were connected to the nerve stumps after cut injury. The recovery of motor function was estimated with walking track analysis at 2, 5, and 8 weeks after surgery. Then immunohistochemical study was performed.
Results: The histological examination showed that only fetal neocortex solid graft cells had survived after implantation. Immunostaining revealed that some of the transplanted cells expressed neural markers such as neurofilament protein and NeuN. But the cells mostly differentiated in glial lineage, which was confirmed with immunostaining for GFAP and S100β. The walking-track analysis has shown that 8 weeks after surgery bioengineered conduit differed significantly from the control.
Conclusions: We revealed that the hydrogel conduit is suitable for nerve re-growth and that the fetal neocortex grafted cells can survive and differentiate. Bioengineered conduit can stimulate functional recovery after the nerve injury.
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http://dx.doi.org/10.1097/GOX.0000000000002610 | DOI Listing |
J Matern Fetal Neonatal Med
December 2025
Department of Obstetrics and Gynecology, Selcuk University Faculty of Medicine, Konya, Turkey.
Introduction: We aim to compare ganglionic eminence (GE) areas between healthy fetuses and those with isolated mild to moderate ventriculomegaly using Magnetic Resonance Imaging (MRI) and assess the postnatal implications of GE area as a marker for neurodevelopmental prognosis.
Material And Methods: A retrospective study was conducted on a cohort of pregnant women who underwent fetal MRI examination between 2018 and 2024. 104 fetuses with bilateral, isolated mild to moderate ventriculomegaly were included in the patient group, and 58 healthy fetuses were included in the control group.
J Biochem
August 2025
Laboratory of Biological Chemistry, Faculty of Applied Biological Sciences, Gifu University, Gifu 501-1193, Japan.
(Pro)renin receptor [(P)RR], encoded by Atp6ap2, is a transmembrane protein found in many organs. It functions in lysosomes as part of the vacuolar-ATPase complex, facilitating autophagy and degradation. Mutations in ATP6AP2 are linked to neurological conditions, including X-linked parkinsonism with spasticity.
View Article and Find Full Text PDFNeuron
July 2025
Center for Regenerative Therapies TU Dresden, TUD Dresden University of Technology, 01307 Dresden, Germany. Electronic address:
Epigenetic mechanisms regulate gene expression programs during neurogenesis, but the extent of epigenetic remodeling during human cortical development remains unknown. Here, we characterize the epigenetic landscape of the human developing neocortex by leveraging Epi-CyTOF, a mass-cytometry-based approach for the simultaneous single-cell analysis of more than 30 epigenetic marks. We identify Polycomb repressive complex 2 (PRC2)-mediated H3K27me3 as the modification with the strongest cell-type-specific enrichment.
View Article and Find Full Text PDFJ Neurosci
August 2025
Department of Anatomy and Neurobiology, Boston University Chobanian and Avedisian School of Medicine, Boston, Massachusetts 02118
Cognitive, social behavior, speech, and motor skills are known challenges for people with trisomy 21/Down syndrome (DS), but the precise mechanisms that lead to these impactful changes have not yet been described. Data from human and mouse model fetal brains indicate that alterations in prenatal neurogenesis might account for the neurological phenotypes that manifest after birth. Here, we evaluated key features of cortical neurogenesis in the humanized mouse model of DS (TcMAC21 of undetermined sex) to test whether and how the presence of the human HSA21q transchromosome impacts cortical development.
View Article and Find Full Text PDFEpilepsia
June 2025
Academic Center for Epileptology, Maastricht University Medical Center and Kempenhaeghe, Heeze, the Netherlands.
One in seven patients with focal epilepsy has a malformation of cortical development (MCD) as underlying cause. Understanding normal cortical development combined with knowledge of where, when, and what goes wrong in different types of MCD provides insight into the mechanisms of epileptogenesis. Three different steps can be distinguished in the development of the neocortex: proliferation, migration, and organization.
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