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Characterization of Subcellular Organelles in Cortical Perisynaptic Astrocytes
Amina Aboufares El Alaoui1,2, Molly Jackson2, Mara Fabri1
1Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.
Frontiers in Cellular Neuroscience
|February 26, 2021
Summary
Perisynaptic astrocytic processes (PAPs) contain diverse organelles like endosomes and mitochondria, challenging previous views of their simplicity. These structures likely support PAPs' crucial roles in regulating neuronal function and synaptic plasticity.
Area of Science:
- Neuroscience
- Cell Biology
- Glial Cell Biology
Background:
- Perisynaptic astrocytic processes (PAPs) are vital for synaptic function, yet their intracellular complexity has been underestimated.
- Traditional electron microscopy suggested PAPs lack organelles, posing a question about how they perform diverse functions.
Purpose of the Study:
- To investigate the three-dimensional ultrastructure of PAPs and their organelle content.
- To determine if PAPs contain sufficient intracellular machinery to support their known functions.
Main Methods:
- Serial block-face scanning electron microscopy (SBF-SEM) was used for high-resolution 3D reconstruction.
- PAPs and their organelles were analyzed in two mouse cortical regions: somatosensory and anterior cingulate cortex.
Main Results:
- Five types of organelles were identified in PAPs: endosomes, phagosomes, mitochondria, and endoplasmic reticulum (ER) cisternae.
- PAPs were categorized into branches, branchlets, and leaflets, with leaflets being most common (~60%).
- Organelle distribution varied by PAP category, with branches showing higher densities of mitochondria and ER cisternae.
Conclusions:
- PAPs possess a rich variety of subcellular organelles, including endosomes, phagosomes, mitochondria, and ER.
- This organelle content provides a structural basis for the diverse functions of PAPs at central synapses.
- The findings revise the understanding of PAP intracellular complexity and their role in synaptic regulation.
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