CD38, CD157, and RAGE as Molecular Determinants for Social Behavior
Open accessAbstract
Recent studies provide evidence to support that cluster of differentiation 38 (CD38) and CD157 meaningfully act in the brain as neuroregulators. They primarily affect social behaviors. Social behaviors are impaired in Cd38 and Cd157 knockout mice. Single-nucleotide polymorphisms of the CD38 and CD157/BST1 genes are associated with multiple neurological and psychiatric conditions, including autism spectrum disorder, Parkinson’s disease, and schizophrenia. In addition, both antigens are related to infectious and immunoregulational processes. The most important clues to demonstrate how these molecules play a role in the brain are oxytocin (OT) and the OT system. OT is axo-dendritically secreted into the brain from OT-containing neurons and causes activation of OT receptors mainly on hypothalamic neurons. Here, we overview the CD38/CD157-dependent OT release mechanism as the initiation step for social behavior. The receptor for advanced glycation end-products (RAGE) is a newly identified molecule as an OT binding protein and serves as a transporter of OT to the brain, crossing over the blood–brain barrier, resulting in the regulation of brain OT levels. We point out new roles of CD38 and CD157 during neuronal development and aging in relation to nicotinamide adenine dinucleotide+ levels in embryonic and adult nervous systems. Finally, we discuss how CD38, CD157, and RAGE are crucial for social recognition and behavior in daily life.
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There are questions surrounding IN-OT's ability to cross the blood-brain barrier and diffuse to subcortical structures.
“and there are questions surrounding its ability to cross the blood-brain barrier and diffuse to subcortical structures [70,71]”
From Translational opportunities for circuit-based social neuroscience: advancing 21st century psychiatry (2021) · cites this paper as [71]
Bypassing the blood-brain barrier remains a perennial problem for pharmacological interventions including IN-OT.
“However, bypassing the blood-brain barrier remains a perennial problem for pharmacological interventions including IN-OT”
From Translational opportunities for circuit-based social neuroscience: advancing 21st century psychiatry (2021) · cites this paper as [71]
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- Authors
- Higashida, H., Hashii, M., Tanaka, Y., Matsukawa, S., Higuchi, Y., Gabata, R., Tsubomoto, M., Seishima, N., Teramachi, M., Kamijima, T., Hattori, T., Hori, O., Tsuji, C., Cherepanov, S. M., Shabalova, A. A., Gerasimenko, M., Minami, K., Yokoyama, S., Munesue, S.-I., Harashima, A., Yamamoto, Y., Salmina, A. B., & Lopatina, O.
- Affiliations
- Kanazawa University (JP)
- Molecular Biology and Chemistry, Faculty of Medical Science, University of Fukui, Fukui 910-1193, Japan
- University of Fukui (JP)
- Suzuka University of Medical Science (JP)
- Department of Basic Research on Social Recognition and Memory, Research Center for Child Mental Development, Kanazawa University, Kanazawa 920-8640, Japan
- Department of Biochemistry and Molecular Vascular Biology, Kanazawa University Graduate School of Medical Sciences, Kanazawa 920-8640, Japan
- Krasnoyarsk State Medical University (RU)
- Corresponding author
- Higashida, Haruhiro
- ORCID
- Venue
- Cells
- Publisher
- MDPI AG
- Published
- 2019-12-25
- Volume
- 9
- Issue
- 1
- Pages
- 62
- ISSN
- 2073-4409 (ISSN-L)
- PMC
- PMC7016687
- OpenAlex
- W2997927572
- Cited by
- 58
- References
- 99
- Citations by year
- 2025: 4 · 2024: 6 · 2023: 13 · 2022: 14 · 2021: 15 · 2020: 5 · 2019: 1
- FWCI
- 1.43
- Type
- journal article
- Language
- en
- Open access
- gold
- dx.doi.org
- Licence
- Locations
- Cells (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Japan Society for the Promotion of Science (18K06501, 18K06521, 18KK0435, 18K06889)
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- CD38, CD157, BST1, RAGE, oxytocin, social behavior, oxytocinergic system, blood-brain barrier, social recognition, NAD+, neuronal development, aging, autism spectrum disorder, schizophrenia, Parkinson's disease, knockout mice, single nucleotide polymorphisms
- MeSH terms
- Receptor for Advanced Glycation End Products, Autism Spectrum Disorder, Animals, Brain, Enzyme Activation, Humans, Immunohistochemistry, Oxytocin, RNA, Messenger, Social Behavior, Biomarkers, Antigens, CD, Mice, Knockout, Gene Expression Regulation, Developmental, Calcium Signaling, Polymorphism, Single Nucleotide, ADP-ribosyl Cyclase, TRPM Cation Channels, ADP-ribosyl Cyclase 1, Genetic Association Studies, GPI-Linked Proteins, Neural Stem Cells
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