Identification of Neuronal Pentraxins as Synaptic Binding Partners of C1q and the Involvement of NP1 in Synaptic Pruning in Adult Mice
Open accessAbstract
Elements of the immune system particularly that of innate immunity, play important roles beyond their traditional tasks in host defense, including manifold roles in the nervous system. Complement-mediated synaptic pruning is essential in the developing and healthy functioning brain and becomes aberrant in neurodegenerative disorders. C1q, component of the classical complement pathway, plays a central role in tagging synapses for elimination; however, the underlying molecular mechanisms and interaction partners are mostly unknown. Neuronal pentraxins (NPs) are involved in synapse formation and plasticity, moreover, NP1 contributes to cell death and neurodegeneration under adverse conditions. Here, we investigated the potential interaction between C1q and NPs, and its role in microglial phagocytosis of synapses in adult mice. We verified in vitro that NPs interact with C1q, as well as activate the complement system. Flow cytometry, immunostaining and co-immunoprecipitation showed that synapse-bound C1q colocalizes and interacts with NPs. High-resolution confocal microscopy revealed that microglia-surrounded C1q-tagged synapses are NP1 positive. We have also observed the synaptic occurrence of C4 suggesting that activation of the classical pathway cannot be ruled out in synaptic plasticity in healthy adult animals. In summary, our results indicate that NPs play a regulatory role in the synaptic function of C1q. Whether this role can be intensified upon pathological conditions, such as in Alzheimer’s disease, is to be disclosed.
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A 2021 study confirmed a role of NPTXs in synaptic pruning by activation of the complement cascade.
“A new study published in 2021, confirmed a role of NPTXs in synaptic pruning by activation of the complement cascade (Kovács et al. 2020).”
From Neuronal pentraxins as biomarkers of synaptic activity: from physiological functions to pathological changes in neurodegeneration (2022) · cites this paper as Kovács et al. 2020
NPTX2 is located in the synaptic cytoplasm and plasma membrane.
“NPTX2 is located in the synaptic cytoplasm and plasma membrane (Kovács et al. 2020).”
From Neuronal pentraxins as biomarkers of synaptic activity: from physiological functions to pathological changes in neurodegeneration (2022) · cites this paper as Kovács et al. 2020
NPTX1 is enriched in the synaptic plasma membrane and also detected in mitochondria.
“NPTX1 is enriched in the synaptic plasma membrane and also detected in mitochondria (in accordance with its role in mitochondrial apoptosis) (Kovács et al. 2020).”
From Neuronal pentraxins as biomarkers of synaptic activity: from physiological functions to pathological changes in neurodegeneration (2022) · cites this paper as Kovács et al. 2020
The recently described role of NPTX1 in synaptic pruning, by activation of the complement-microglia axis, could be intensified upon neurodegeneration.
“The recently described role of NPTX1 in synaptic pruning, by activation of the complement-microglia axis, could be intensified upon neurodegeneration (Kovács et al. 2020) (Fig. 3b-5).”
From Neuronal pentraxins as biomarkers of synaptic activity: from physiological functions to pathological changes in neurodegeneration (2022) · cites this paper as Kovács et al. 2020
NPTX1 participates in synaptic pruning by activation of the classical complement cascade.
“Moreover, it participates in synaptic pruning by activation of the classical complement cascade (Kovács et al. 2020) (Fig. 3a-5) and may act as a sensor of harmful stimuli, targeting affected neurons to apoptotic cell death (Clayton et al. 2012; Rahim et al. 2013).”
From Neuronal pentraxins as biomarkers of synaptic activity: from physiological functions to pathological changes in neurodegeneration (2022) · cites this paper as Kovács et al. 2020
NPTX deregulation could lead to an imbalance in synaptogenesis/synaptic pruning.
“In addition, NPTXs deregulation could lead to an imbalance in synaptogenesis/synaptic pruning (Kovács et al. 2020).”
From Neuronal pentraxins as biomarkers of synaptic activity: from physiological functions to pathological changes in neurodegeneration (2022) · cites this paper as Kovács et al. 2020
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References 76 · Cited by 43
- Authors
- Kovács, R. Á., Vadászi, H., Bulyáki, É., Török, G., Tóth, V., Mátyás, D., Kun, J., Hunyadi-Gulyás, É., Fedor, F. Z., Csincsi, Á., Medzihradszky, K., Homolya, L., Juhász, G., Kékesi, K. A., Józsi, M., Györffy, B. A., & Kardos, J.
- Affiliations
- Eötvös Loránd University (HU)
- Semmelweis University (HU)
- HUN-REN Szegedi Biológiai Kutatóközpont (HU)
- Institute of Molecular Life Sciences (HU)
- Corresponding author
- Kardos, József
- ORCID
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2021-02-08
- Volume
- 11
- Pages
- 599771-599771
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC7897678
- OpenAlex
- W3127928580
- Cited by
- 43
- References
- 76
- Citations by year
- 2026: 6 · 2025: 6 · 2024: 9 · 2023: 11 · 2022: 9 · 2021: 2
- FWCI
- 3.10
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Repository of the Academy's Library (Library of the Hungarian Academy of Sciences) (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- ELTE Digital Institutional Repository (EDIT) (Eötvös Loránd University) (submittedVersion, cc-by)
- Funders
- Nemzeti Kutatási, Fejlesztési és Innovaciós Alap (KTIA_NAP_13-2-2014-0017, 2017-1.2.1-NKP-2017-00002, FIEK_16-1-2016-0005, VEKOP-2.3.3-15-2016-00007, K128123)
- Emberi Eroforrások Minisztériuma (NTP-NFTÖ-19-B-0057)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › Complement system in diseases
- Life Sciences › Immunology and Microbiology › Immunology › Biomarkers in Disease Mechanisms
- Keywords
- C1q, synaptic pruning, complement system, microglial phagocytosis, C4, synaptic plasticity, neurodegeneration, Alzheimer's disease
- MeSH terms
- Pentraxins, Alzheimer Disease, Animals, C-Reactive Protein, Complement C4, Male, Nerve Tissue Proteins, Phagocytosis, Synapses, Complement C1q, Microglia, Mice
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