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Related Concept Videos

Neurogenesis and Regeneration of Nervous Tissue01:15

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In the CNS, neurogenesis, the birth of new neurons from stem cells, is limited to the hippocampus in adults. In other regions of the brain and spinal cord, neurogenesis is almost non-existent due to inhibitory influences from neuroglia, especially oligodendrocytes, and the absence of growth-stimulating cues. The myelin produced by oligodendrocytes in the CNS inhibits neuronal regeneration. Furthermore, astrocytes proliferate rapidly after neuronal damage, forming scar tissue that physically...
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Neurogenesis and Neuroinflammation in Dialogue: Mapping Gaps, Modulating Microglia, Rewiring Aging.

Masaru Tanaka1

  • 1Danube Neuroscience Research Laboratory, HUN-REN-SZTE Neuroscience Research Group, Hungarian Research Network, University of Szeged, Tisza Lajos krt. 113, H-6725 Szeged, Hungary.

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|January 9, 2026
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Aging brains face declining neurogenesis and rising neuroinflammation, termed inflammaging. Strategies like immunomodulation and epigenetic editing can restore cognitive function by reprogramming this interaction.

Keywords:
Alzheimer diseaseaging braincognitive declineepigeneticshippocampusinflammasomesmicroglianeurogenesisneuroinflammationtranslational research

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Area of Science:

  • Neuroscience
  • Immunology
  • Aging Research

Background:

  • Aging brains exhibit declining neurogenesis and increasing neuroinflammation, a process known as inflammaging.
  • This convergence impairs synaptic plasticity and cognitive function due to maladaptive glial states.
  • Critical knowledge gaps exist in microglial heterogeneity, epigenetic mechanisms, and immune responses within the brain niche.

Purpose of the Study:

  • To address knowledge gaps in the aging brain's neurogenesis and neuroinflammation dialogue.
  • To evaluate strategies for reprogramming the interaction between neurogenesis and neuroinflammation.
  • To provide a roadmap for delaying cognitive decline through mechanistic precision.

Main Methods:

  • Review of current literature on neurogenesis and neuroinflammation in aging.
  • Identification of five major knowledge gaps in the field.
  • Evaluation of strategies including longitudinal imaging, immunomodulation, glial reprogramming, inflammasome inhibitors, and epigenetic editing.

Main Results:

  • Neurogenesis potential can be preserved or restored in aging brains.
  • Tuning the immune and epigenetic environments is key to maintaining cognitive function.
  • Mechanistic precision in interventions can guide clinical innovation for neurodegenerative diseases.

Conclusions:

  • Neurogenic potential is not lost with age but can be modulated by immune and epigenetic factors.
  • A roadmap is proposed for reshaping the aging brain's trajectory and delaying cognitive decline.
  • Integrating cellular plasticity with immune modulation offers a path to re-engineer resilience across the lifespan.