Release of insulin produced by the choroid plexis is regulated by serotonergic signaling
Open accessAbstract
The choroid plexus (ChP) is a highly vascularized tissue found in the brain ventricles, with an apical epithelial cell layer surrounding fenestrated capillaries. It is responsible for the production of most of the cerebrospinal fluid (CSF) in the ventricular system, subarachnoid space, and central canal of the spinal cord, while also constituting the blood-CSF barrier (BCSFB). In addition, epithelial cells of the ChP (EChP) synthesize neurotrophic factors and other signaling molecules that are released into the CSF. Here, we show that insulin is produced in EChP of mice and humans, and its expression and release are regulated by serotonin. Insulin mRNA and immune-reactive protein, including C-peptide, are present in EChP, as detected by several experimental approaches, and appear in much higher levels than any other brain region. Moreover, insulin is produced in primary cultured mouse EChP, and its release, albeit Ca2+ sensitive, is not regulated by glucose. Instead, activation of the 5HT2C receptor by serotonin treatment led to activation of IP3-sensitive channels and Ca2+ mobilization from intracellular storage, leading to insulin secretion. In vivo depletion of brain serotonin in the dorsal raphe nucleus negatively affected insulin expression in the ChP, suggesting an endogenous modulation of ChP insulin by serotonin. Here, we show for the first time to our knowledge that insulin is produced by EChP in the brain, and its release is modulated at least by serotonin but not glucose.
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Ins2 expression in the 3V ChP supports the model that the ChP is an internal source of insulin for the brain.
“For example, Ins2 was expressed in the 3V ChP, supporting the model that the ChP is an internal source of insulin for the brain (Mazucanti et al., 2019).”
From A cellular and spatial map of the choroid plexus across brain ventricles and ages (2021) · cites this paper as Mazucanti et al., 2019
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References 78 · Cited by 101
- Authors
- Mazucanti, C. H., Liu, Q.-R., Lang, D., Huang, N., O’Connell, J. F., Camandola, S., & Egan, J. M.
- Affiliations
- National Institute on Aging (US)
- ORCID
- Venue
- JCI Insight
- Published
- 2019-12-05
- Volume
- 4
- Issue
- 23
- ISSN
- 2379-3708 (ISSN-L)
- PMC
- PMC6962018
- OpenAlex
- W2982026481
- Cited by
- 101
- References
- 78
- Citations by year
- 2026: 9 · 2025: 18 · 2024: 11 · 2023: 21 · 2022: 18 · 2021: 18 · 2020: 5 · 2018: 1
- FWCI
- 4.89
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- JCI Insight (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Amylin Pharmaceuticals
- Gilead Sciences
- National Institutes of Health
- National Institute on Aging
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Cerebrospinal fluid and hydrocephalus
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- choroid plexus, insulin, serotonin, insulin secretion, cerebrospinal fluid, choroid plexus epithelial cells, dorsal raphe nucleus, calcium mobilization, IP3 receptor, blood-CSF barrier, C-peptide
- MeSH terms
- Animals, Blood-Brain Barrier, Brain, Calcium, Cerebrospinal Fluid, Choroid Plexus, Epithelial Cells, Glucose, Humans, Insulin, Male, Mice, Inbred C57BL, RNA, Messenger, Serotonin, Signal Transduction, Gene Expression, Mice, Molecular Docking Simulation
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