Evidence map›Paper›PMID 38087165›Full record

ArticleMolecular neurobiology2024

Pathological Deficit of Cystatin B Impairs Synaptic Plasticity in EPM1 Human Cerebral Organoids.

Amelia Pizzella, Eduardo Penna, Natalia Abate, Elisa Frenna, Laura Canafoglia, Francesca Ragona, Rosita Russo, Angela Chambery, Carla Perrone-Capano, Silvia Cappello and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

Amelia PizzellaDepartment of Biology, University of Naples Federico II, Naples, Italy.
Eduardo PennaDepartment of Biology, University of Naples Federico II, Naples, Italy.
Natalia AbateDepartment of Biology, University of Naples Federico II, Naples, Italy.
Elisa FrennaDepartment of Biology, University of Naples Federico II, Naples, Italy.
Laura CanafogliaIntegrated Diagnostics for Epilepsy, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Francesca RagonaDepartment of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Rosita RussoDepartment of Environmental, Biological and Pharmaceutical Sciences and Technologies, University of Campania "Luigi Vanvitelli, Caserta, Italy.
Angela ChamberyDepartment of Environmental, Biological and Pharmaceutical Sciences and Technologies, University of Campania "Luigi Vanvitelli, Caserta, Italy.
Carla Perrone-CapanoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Silvia CappelloDepartment of Developmental Neurobiology, Max Planck Institute of Psychiatry, Munich, Germany.
Marianna CrispinoDepartment of Biology, University of Naples Federico II, Naples, Italy. crispino@unina.it.ORCID http://orcid.org/0000-0002-5797-8830
Rossella Di GiaimoDepartment of Biology, University of Naples Federico II, Naples, Italy. digiaimo@unina.it.
Max Planck Institute of Psychiatry · DEUniversity of Naples Federico II · ITFederico II University Hospital · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITUniversity of Campania "Luigi Vanvitelli" · IT

Funding

Università degli Studi di Napoli Federico II FRA 2022 tipologia A
6 · The paper itself

Abstract

Cystatin B (CSTB) is a small protease inhibitor protein being involved in cell proliferation and neuronal differentiation. Loss-of-function mutations in CSTB gene cause progressive myoclonic epilepsy 1 (EPM1). We previously demonstrated that CSTB is locally synthesized in synaptic nerve terminals from rat brain and secreted into the media, indicating its role in synaptic plasticity. In this work, we have further investigated the involvement of CSTB in synaptic plasticity, using synaptosomes from human cerebral organoids (hCOs) as well as from rodents' brain. Our data demonstrate that CSTB is released from synaptosomes in two ways: (i) as a soluble protein and (ii) in extracellular vesicles-mediated pathway. Synaptosomes isolated from hCOs are enriched in pre-synaptic proteins and contain CSTB at all developmental stages analyzed. CSTB presence in the synaptic territories was also confirmed by immunostaining on human neurons in vitro. To investigate if the depletion of CSTB affects synaptic plasticity, we characterized the synaptosomes from EPM1 hCOs. We found that the levels of presynaptic proteins and of an initiation factor linked to local protein synthesis were both reduced in EPM1 hCOs and that the extracellular vesicles trafficking pathway was impaired. Moreover, EPM1 neurons displayed anomalous morphology with longer and more branched neurites bearing higher number of intersections and nodes, suggesting connectivity alterations. In conclusion, our data strengthen the idea that CSTB plays a critical role in the synapse physiology and reveal that pathologically low levels of CSTB may affect synaptic plasticity, leading to synaptopathy and altered neuronal morphology.

Indexed as

Cystatin BNeuronal PlasticityOrganoidsSynaptosomesAnimalsCerebral CortexExtracellular VesiclesHumansMyoclonic Epilepsies, ProgressiveNeuronsRatsSynapsesCystatin BCystatin BEPM1Extracellular vesiclesHuman cerebral organoidsSynaptic plasticitySynaptosomes

Identifiers

PMID38087165
PMCPMC11236866
OpenAlexW4389609555

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.