Differences in Anatomical Outcomes Between Early Chronic and Far Chronic Time-Points After Transplantation of Spinal Cord Neural Progenitor Cells in Mice DOI

Angelina Baltazar,

Ashley Tucker,

Julius Jang

et al.

Journal of Neurotrauma, Journal Year: 2023, Volume and Issue: 40(23-24), P. 2487 - 2499

Published: Aug. 19, 2023

Spinal cord injury (SCI) affects millions of people worldwide. Neural progenitor cell (NPC) transplantation is a promising treatment for regenerating lost spinal tissue and restoring neurological function after SCI. We conducted literature search found that less than quarter experimental rodent studies have investigated anatomical outcomes at longer 4 months post-transplantation. This critical topic to investigate, given stem therapies would need remain in place throughout the lifetime an individual. sought determine how commonly assessed evolve between early far chronic time-points post-NPC transplantation. At either 8 weeks or 26 following NPCs into sites cervical SCI, we evaluated graft neuronal density, astroglial axon outgrowth, regeneration host populations grafts male female mice. density does not change over time, but numbers graft-associated astrocytes glial fibrillary acidic protein intensity significantly increased phase compared with time-point. In addition, outgrowth was decreased post-transplantation contrast, corticospinal diminished rather from periods. Interestingly, influenced by sex animal, suggesting sex-dependent processes may shape composition time. Collectively, these results demonstrate NPC transplants are dynamic outcome measures associated efficacy cord.

Language: Английский

Implications of altered pyramidal cell morphology on clinical symptoms of neurodevelopmental disorders DOI Open Access

Zummar Asad,

Yara Fakheir,

Yara Abukhaled

et al.

European Journal of Neuroscience, Journal Year: 2024, Volume and Issue: 60(5), P. 4877 - 4892

Published: July 25, 2024

The prevalence of pyramidal cells (PCs) in the mammalian cerebral cortex underscore their value as they play a crucial role various brain functions, ranging from cognition, sensory processing, to motor output. PC morphology significantly influences connectivity and plays critical maintaining normal function. Pathological alterations are thought contribute aetiology neurodevelopmental disorders such autism spectrum disorder (ASD) schizophrenia. This review explores relationship between abnormalities key cortical areas clinical manifestations schizophrenia ASD. We focus largely on human postmortem studies provide evidence that dendritic segment length, complexity spine density differentially affected these disorders. These morphological can lead disruptions connectivity, potentially contributing cognitive behavioural deficits observed Furthermore, we highlight importance investigating functional structural characteristics PCs illuminate underlying pathogenesis stimulate further research this area.

Language: Английский

Citations

0

Synapse weakening-induced caspase-3 activity confers specificity to microglia-mediated synapse elimination DOI Creative Commons
Zhou Yu, Andrian Gutu, Nam-Soo Kim

et al.

bioRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown

Published: Aug. 5, 2024

Abstract During brain development, synapses are initially formed in excess and later eliminated an activity-dependent manner, with weak being preferentially removed. Previous studies identified glia as mediators of synapse removal, but it is unclear how specifically target synapses. Here we show that, the developing mouse visual pathway, inhibiting synaptic transmission induces postsynaptic activation caspase-3. Caspase-3 essential for elimination driven by both spontaneous experience-dependent neural activity. Synapse weakening-induced caspase-3 determines specificity mediated microglia not astrocytes. Furthermore, a model Alzheimer’s disease, deficiency protects against loss induced amyloid-β deposition. Our results reveal key step during development neurodegeneration.

Language: Английский

Citations

0

Synapse weakening-induced caspase-3 activity confers specificity to microglia-mediated synapse elimination DOI Open Access
Zhou Yu, Andrian Gutu, Nam-Soo Kim

et al.

Published: Oct. 18, 2024

During brain development, synapses are initially formed in excess and later eliminated an activity-dependent manner, with weak being preferentially removed. Previous studies identified glia as mediators of synapse removal, but it is unclear how specifically target synapses. Here we show that, the developing mouse visual pathway, inhibiting synaptic transmission induces postsynaptic activation caspase-3. Caspase-3 essential for elimination driven by both spontaneous experience-dependent neural activity. Synapse weakening-induced caspase-3 determines specificity mediated microglia not astrocytes. Furthermore, a model Alzheimer’s disease, deficiency protects against loss induced amyloid-β deposition. Our results reveal key step during development neurodegeneration.

Language: Английский

Citations

0

Synapse weakening-induced caspase-3 activity confers specificity to microglia-mediated synapse elimination DOI Open Access
Zhou Yu, Andrian Gutu, Nam-Soo Kim

et al.

Published: Oct. 18, 2024

During brain development, synapses are initially formed in excess and later eliminated an activity-dependent manner, with weak being preferentially removed. Previous studies identified glia as mediators of synapse removal, but it is unclear how specifically target synapses. Here we show that, the developing mouse visual pathway, inhibiting synaptic transmission induces postsynaptic activation caspase-3. Caspase-3 essential for elimination driven by both spontaneous experience-dependent neural activity. Synapse weakening-induced caspase-3 determines specificity mediated microglia not astrocytes. Furthermore, a model Alzheimer’s disease, deficiency protects against loss induced amyloid-β deposition. Our results reveal key step during development neurodegeneration.

Language: Английский

Citations

0

Differences in Anatomical Outcomes Between Early Chronic and Far Chronic Time-Points After Transplantation of Spinal Cord Neural Progenitor Cells in Mice DOI

Angelina Baltazar,

Ashley Tucker,

Julius Jang

et al.

Journal of Neurotrauma, Journal Year: 2023, Volume and Issue: 40(23-24), P. 2487 - 2499

Published: Aug. 19, 2023

Spinal cord injury (SCI) affects millions of people worldwide. Neural progenitor cell (NPC) transplantation is a promising treatment for regenerating lost spinal tissue and restoring neurological function after SCI. We conducted literature search found that less than quarter experimental rodent studies have investigated anatomical outcomes at longer 4 months post-transplantation. This critical topic to investigate, given stem therapies would need remain in place throughout the lifetime an individual. sought determine how commonly assessed evolve between early far chronic time-points post-NPC transplantation. At either 8 weeks or 26 following NPCs into sites cervical SCI, we evaluated graft neuronal density, astroglial axon outgrowth, regeneration host populations grafts male female mice. density does not change over time, but numbers graft-associated astrocytes glial fibrillary acidic protein intensity significantly increased phase compared with time-point. In addition, outgrowth was decreased post-transplantation contrast, corticospinal diminished rather from periods. Interestingly, influenced by sex animal, suggesting sex-dependent processes may shape composition time. Collectively, these results demonstrate NPC transplants are dynamic outcome measures associated efficacy cord.

Language: Английский

Citations

0