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Isolation and Characterization of the Immune Cells from Micro-dissected Mouse Choroid Plexuses
Published on: February 3, 2022
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Morphological and mitochondrial changes in murine choroid plexus epithelial cells during healthy aging
Valentina Scarpetta1,2, Felipe Bodaleo3, Chiara Salio4
1Department of Neurosciences Rita Levi Montalcini, University of Turin, 10126, Turin, Italy.
Fluids and Barriers of the CNS
|March 15, 2023
Summary
Healthy aging causes significant morpho-functional changes in choroid plexus epithelial cells, impacting the blood-cerebrospinal fluid barrier. These age-related alterations in the choroid plexus appear early and persist throughout adulthood.
Area of Science:
- Neuroscience
- Cell Biology
- Aging Research
Background:
- Choroid plexuses (ChPs) form the blood-cerebrospinal fluid barrier, crucial for brain homeostasis.
- ChP dysfunction is linked to neurodegenerative disease progression.
- Understanding ChP aging is vital for brain health.
Purpose of the Study:
- To map morpho-functional changes in ChP epithelial cells during aging in mice.
- To investigate age-related alterations from young adulthood to 2 years old.
- To correlate structural and functional changes in aging ChP.
Main Methods:
- Utilized transmission electron microscopy (TEM) and 2-photon microscopy (2-PM).
- Employed immunohistochemistry, RT-qPCR, and Western Blot.
- Analyzed ChP tissues at multiple timepoints in aging mice.
Main Results:
- Identified epithelial flattening, reduced microvilli, and increased tight junction interruptions from 8-12 months.
- Observed decreased mitochondrial density, elongated mitochondria, increased superoxide, and reduced membrane potential in aged mice.
- Noted that most changes occurred without significant gene/protein expression shifts, and aged mitochondria remained responsive.
Conclusions:
- Aging induces progressive morpho-functional changes in mouse choroid plexus epithelium.
- Structural remodeling of the ChP occurs throughout the aging process.
- Findings offer insights into the correlation between ChP rearrangements and aging.

