Evidence map›Paper›PMID 40899734›Full record

ArticleJournal of neurochemistry2025

Reelin Increases the Sphingomyelin Content of the Plasma Membrane and Affects the Surface Expression of GPI-Anchored Proteins in Hippocampal Neurons.

Yuto Takekoshi, Hugo Ando, Takao Kohno, Hiroshi Takase, Tomohiko Taguchi, Makoto Arita, Toshihide Kobayashi, Mitsuharu Hattori

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Yuto TakekoshiDepartment of Biomedical Science, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, Aichi, Japan.
Hugo AndoDepartment of Biomedical Science, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, Aichi, Japan.
Takao KohnoDepartment of Biomedical Science, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, Aichi, Japan.ORCID https://orcid.org/0000-0003-2557-4281
Hiroshi TakaseCore Laboratory, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Aichi, Japan.
Tomohiko TaguchiLaboratory of Organelle Pathophysiology, Department of Integrative Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai, Miyagi, Japan.
Makoto AritaLaboratory for Metabolomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Toshihide KobayashiLaboratoire de Bioimagerie et Pathologies, UMR 7021 CNRS, Faculté de Pharmacie, Université de Strasbourg, Illkirch, France.
Mitsuharu HattoriDepartment of Biomedical Science, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, Aichi, Japan.ORCID https://orcid.org/0000-0002-0503-4969

Funding

Japan Society for the Promotion of Science JP20H03384Japan Society for the Promotion of Science JP23K27324Japan Society for the Promotion of Science JP24KJ1889Ministry of Education, Culture, Sports, Science and Technology JPMXS044-500025Nagoya City University 2401101Support for Pioneering Research Initiated by the Next Generation (SPRING) in Japan Science and Technology Agency JPMJSP2130Terumo Foundation for Life Sciences and Arts
6 · The paper itself

Abstract

Sphingomyelin (SM) is primarily located in the outer leaflet of the plasma membrane. It plays a crucial role in intercellular communication and the morphology of neuronal cells by influencing the localization and function of various proteins. However, the mechanisms regulating the SM content in the neuronal plasma membrane remain largely elusive. In this study, we discovered that Reelin, an important secreted signaling protein in the central nervous system, increases the SM content of the plasma membrane of cultured hippocampal neurons by promoting SM synthesis using a SM specific probe and a fluorescently labeled SM precursor molecule. This increase in SM was associated with increased surface expression of glycosylphosphatidylinositol (GPI)-anchored proteins analyzed by immunohistochemistry or using phosphatidylinositol-specific phospholipase C, suggesting a functional link between SM levels and membrane protein trafficking. Furthermore, comparative lipidomic analysis of the postsynaptic density fraction by LC-MS/MS revealed distinct alterations in SM-related lipid species between wild-type and Reelin-deficient mice. These findings suggest that Reelin regulates the SM content in the neuronal plasma membrane, which, in turn, affects the function and morphology of the neuron by affecting the surface levels of GPI-anchored proteins. These findings identify a novel role for Reelin in modulating neuronal membrane lipid composition, which may underlie its diverse functions in neuronal development and synaptic plasticity in both the developing and adult brain.

Indexed as

Cell Adhesion Molecules, NeuronalCell MembraneExtracellular Matrix ProteinsGlycosylphosphatidylinositolsHippocampusNerve Tissue ProteinsNeuronsSerine EndopeptidasesSphingomyelinsAnimalsCells, CulturedGPI-Linked ProteinsMiceMice, Inbred C57BLMice, KnockoutRatsCell Adhesion Molecules, NeuronalExtracellular Matrix ProteinsGlycosylphosphatidylinositolsGPI-Linked ProteinsNerve Tissue ProteinsReelin ProteinReln protein, mouseSerine EndopeptidasesSphingomyelinsmembraneneuronreelinsphingomyelin

Identifiers

PMID40899734
PMCPMC12406644

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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 OpenQuestion graph.