Choroid Plexus in Alzheimer’s Disease—The Current State of Knowledge
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The choroid plexus (CP), located in each of the four ventricles of the brain, is formed by a monolayer of epithelial cells that surrounds a highly vascularized connective tissue with permeable capillaries. These cells are joined by tight junctions forming the blood–cerebrospinal fluid barrier (BCSFB), which strictly regulates the exchange of substances between the blood and cerebrospinal fluid (CSF). The primary purpose of the CP is to secrete CSF, but it also plays a role in the immune surveillance of the central nervous system (CNS) and in the removal of neurotoxic compounds from the CSF. According to recent findings, the CP is also involved in the modulation of the circadian cycle and neurogenesis. In diseases such as Alzheimer’s disease (AD), the function of the CP is impaired, resulting in an altered secretory, barrier, transport, and immune function. This review describes the current state of knowledge concerning the roles of the CP and BCSFB in the pathophysiology of AD and summarizes recently proposed therapies that aim to restore CP and BCSFB functions.
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BCSFB disruption in AD is induced by proinflammatory cytokines or matrix metalloproteinase (MMP) expressed by choroid plexus epithelial cells.
“Numerous studies have revealed AD associated BCSFB disruption induced by proinflammatory cytokines or matrix metalloproteinase (MMP) expressed by CP epithelial cells.”
From Role of neuroinflammation in neurodegeneration development (2023) · cites this paper as [144]
Section 6.3 links increased MMP levels in the choroid plexus to BCSFB leakage, but says they may compromise barrier integrity. Section 6.6 reports that blocking TNF signaling restored BCSFB integrity in AD mouse models. The review does not establish that MMPs are specifically expressed by choroid plexus epithelial cells or that these factors definitively induce BCSFB disruption in AD patients; page numbers were unavailable in our copy. (LLM, conf=0.84)
Experimental — accuracy not yet measuredCP displays important function in removal of neurotoxic compounds (e.g., Aβ plaques) from CSF.
“In addition, CP also displays important function in the removal of neurotoxic compounds (e.g., Aβ plaques) from the CSF.144”
From Role of neuroinflammation in neurodegeneration development (2023) · cites this paper as [144]
Section 6.2 says the choroid plexus assists in removing harmful compounds from CSF, and Section 6.4 describes transport of Aβ peptide from CSF toward the bloodstream. The paper does not say that the choroid plexus removes Aβ plaques from CSF; that example is more specific than the evidence supports. No page numbers were provided in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measuredBCSFB disruption impairs its selectivity, leading to increased infiltration of cytokines and leukocytes into the CSF, which then activate glial cells in the CNS.
“BCSFB disruption impaired the selectivity of it, leading to increased infiltration of cytokines and leukocytes into the CSF which then activated glial cells in the CNS.”
From Role of neuroinflammation in neurodegeneration development (2023) · cites this paper as [144]
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Cited by
Sorted by citations
Role of neuroinflammation in neurodegeneration development
Zhang, W., Xiao, D., Mao, Q., & Xia, H. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01486-5 · Cited by 1,668 · see citing works
“BCSFB disruption impaired the selectivity of it, leading to increased infiltration of cytokines and leukocytes into the CSF which then activated glial cells in the CNS.144,145 BCSFB acts as a gateway for inflammationresolving leukocyte entry into the CSF during immune responses through the constitutively expressed adh…”
BackgroundInfluentialYazdan-Panah, A., Schmidt-Mengin, M., Ricigliano, V. A. G., Soulier, T., Stankoff, B., & Colliot, O. (2023) · NeuroImage: Clinical · doi:10.1016/j.nicl.2023.103368 · Cited by 58 · see citing works
- Authors
- Gião, T., Teixeira, T., Almeida, M. R., & Cardoso, I.
- Affiliations
- Universidade do Porto (PT)
- Corresponding author
- Gião, Tiago
- Cardoso, Isabel
- Venue
- Biomedicines
- Publisher
- MDPI AG
- Published
- 2022-01-21
- Volume
- 10
- Issue
- 2
- Pages
- 224
- ISSN
- 2227-9059 (ISSN-L)
- PMC
- PMC8869376
- OpenAlex
- W4205289271
- Cited by
- 64
- References
- 8
- Citations by year
- 2026: 14 · 2025: 13 · 2024: 20 · 2023: 11 · 2022: 6
- FWCI
- 1.89
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Biomedicines (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Fundação para a Ciência e Tecnologia (PTDC/MED-PAT/0959/2021, 2020.07444.BD)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Cerebrospinal fluid and hydrocephalus
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- choroid plexus, Alzheimer's disease, blood-CSF barrier, cerebrospinal fluid production, tight junctions, choroid plexus epithelial cells, circadian rhythm, neurogenesis
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