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ER is the primary site for the maturation and folding of soluble and transmembrane secretory proteins. The calnexin cycle is a specific chaperone system that folds and assesses the confirmation of N-glycosylated proteins before they can exit the ER lumen. The primary players of this quality check pipeline are the lectins, ER-resident chaperones, and a glucosyl transferase enzyme. In case the calnexin system in the lumen fails to salvage a misfolded protein, it is transported to the cytoplasm...
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Related Experiment Video

Updated: May 3, 2026

Three-dimensional Confocal Analysis of Microglia/macrophage Markers of Polarization in Experimental Brain Injury
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Microglia Display Altered Spatial Morphology and Proteome After Stroke.

Brooke J Wanrooy1, Jenny L Wilson1, Althea R Suthya1

  • 1Centre For Inflammatory Diseases, Department of Medicine, School of Clinical Sciences At Monash Health, Monash University, Victoria, Clayton, Australia.

Proteomics
|November 10, 2025
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Summary

Ischaemic stroke alters the brain microenvironment, significantly impacting microglia morphology and function. These immune cells show region-specific changes, influencing inflammatory signaling pathways crucial for stroke recovery.

Keywords:
microgliamorphologyneuroinflammationproteomestroke

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Area of Science:

  • Neuroscience
  • Immunology
  • Stroke Research

Background:

  • Microglia are key immune cells in the central nervous system (CNS), essential for neural development and homeostasis.
  • They act as immune sentinels, constantly monitoring the neural environment and reacting to brain insults.

Purpose of the Study:

  • To investigate how the cerebral microenvironment, altered by ischaemic stroke, impacts microglial morphology and function in a spatially dependent manner.
  • To identify molecular changes in microglia following stroke.

Main Methods:

  • Transient middle cerebral artery occlusion (tMCAO) model in rodents.
  • Analysis of regional gene expression, microglial morphology via 3D reconstruction, and unbiased proteomics at 24 hours post-stroke.
  • Isolation of microglia from ipsilateral and contralateral hemispheres.

Main Results:

  • The infarct core exhibits a distinct proinflammatory microenvironment compared to sham controls.
  • Stroke induces region-specific microglial morphological changes, with amoeboid shapes and reduced complexity near the infarct.
  • 108 differentially expressed proteins were identified in microglia, implicating pathways in cytokine production, chemokine activity, and leukocyte migration.

Conclusions:

  • Microglia morphology and function are significantly altered by ischaemic stroke in a region-specific manner.
  • These changes are linked to distinct inflammatory profiles and protein expression changes within the brain.
  • Microglia play critical roles in regulating inflammatory signaling post-stroke.