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Related Experiment Video

Updated: May 28, 2026

In Vivo Chronic Two-Photon Imaging of Microglia in the Mouse Hippocampus
07:03

In Vivo Chronic Two-Photon Imaging of Microglia in the Mouse Hippocampus

Published on: July 6, 2022

Microglia in the normally aged hippocampus.

Jung Hoon Choi1, Moo-Ho Won

  • 1Department of Anatomy, College of Veterinary Medicine, Kangwon National University, Chuncheon, Korea.

Laboratory Animal Research
|October 15, 2011
PubMed
Summary
This summary is machine-generated.

Aging impairs the hippocampus, crucial for memory and navigation. This review examines how changes in microglia, the brain's immune cells, relate to these age-related hippocampal declines.

Keywords:
Agingbrainimmune cellsmemory

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Immunofluorescence Staining Using IBA1 and TMEM119 for Microglial Density, Morphology and Peripheral Myeloid Cell Infiltration Analysis in Mouse Brain

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Last Updated: May 28, 2026

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Immunofluorescence Staining Using IBA1 and TMEM119 for Microglial Density, Morphology and Peripheral Myeloid Cell Infiltration Analysis in Mouse Brain

Published on: October 27, 2019

Area of Science:

  • Neuroscience
  • Aging Research
  • Immunology

Background:

  • The hippocampus is vital for memory and spatial navigation.
  • Aging leads to hippocampus functional decline and increased susceptibility to degenerative diseases.
  • Microglia are the primary immune cells in the central nervous system, responding to brain changes.

Purpose of the Study:

  • To review the morphological and functional changes in the hippocampus during aging.
  • To examine the role and changes of microglia in the aging brain.
  • To explore the relationship between hippocampal and microglial alterations in aging.

Main Methods:

  • Literature review of studies on aging, hippocampus, and microglia.
  • Analysis of morphological and functional changes in both hippocampus and microglia.
  • Correlation of age-related changes between the hippocampus and microglia.

Main Results:

  • Aging is associated with functional and structural decline in the hippocampus.
  • Microglia exhibit significant morphological and functional alterations in the aged brain.
  • Hippocampal changes during aging are closely linked to microglial activation and changes.

Conclusions:

  • Microglial changes are integral to the aging process within the hippocampus.
  • Understanding the hippocampus-microglia interaction is key to addressing age-related cognitive decline.
  • Further research into microglial modulation may offer therapeutic strategies for aging brains.