Evidence map›Paper›PMID 39756866›Full record

ArticleCell structure and function2025

Magnetic control of membrane damage in early endosomes using internalized magnetic nanoparticles.

Yuta Yonekawa, Kazuki Oikawa, Boldbaatar Bayarkhuu, Kizuna Kobayashi, Nana Saito, Ibuki Oikawa, Ryohei Yamada, Yu-Han Chen, Koichi Oyanagi, Yuji Shibasaki and 2 more

Abstract read
In one paragraph

Article in Cell structure and function, 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. Review
  2. Review
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.

Yuta YonekawaGraduate Course in Biological Sciences, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Kazuki OikawaGraduate Course in Biological Sciences, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Boldbaatar BayarkhuuGraduate Course in Biological Sciences, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Kizuna KobayashiGraduate Course in Biological Sciences, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Nana SaitoGraduate Course in Biological Sciences, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Ibuki OikawaGraduate Course in Materials Science and Engineering, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Ryohei YamadaGraduate Course in Materials Science and Engineering, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Yu-Han ChenDepartment of Biochemical Science and Technology, National Chiayi University.
Koichi OyanagiGraduate Course in Materials Science and Engineering, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Yuji ShibasakiGraduate Course in Chemistry, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Satoru KobayashiGraduate Course in Materials Science and Engineering, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.
Yoko ShibaGraduate Course in Biological Sciences, Division of Science and Engineering, Graduate School of Arts and Sciences, Iwate University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane stiffness is essential for cell migration, tumorigenesis, and development; however, the physical properties of intracellular membrane are poorly characterized. In this study, we internalized 20 nm magnetic nanoparticles (MNPs) into MCF7 human breast cancer cells and applied a magnetic field. We investigated whether magnetic field could induce membrane damage of the early endosomes by analyzing the colocalization of MNPs with galectin 3 (Gal3), a cytosolic protein recruited to the lumen of damaged organelles. We first tried to apply magnetic field by electromagnet, and found a direct-current (DC) magnetic field for five minutes increased the colocalization of the MNPs with Gal3, suggesting that the magnetic field damaged the endosomal membrane. We used a neodymium magnet to apply longer and stronger static magnetic fields. The static magnetic field more than 50 mT for five minutes started to damage endosomes, while 100 mT was the most effective. Longer exposure or higher magnetic field strengths did not induce further membrane damage. We confirmed that a Gal3 positive compartment was also positive for the early endosome marker, EEA1, suggesting that the external magnetic field induced membrane damage in the early endosomes. Our results indicate that a static magnetic field can control the membrane damage in early endosomes using internalized MNPs.Key words: magnetic nanoparticles, endosomes, membrane damage, organelle.

Indexed as

Cell MembraneEndosomesMagnetic FieldsMagnetite NanoparticlesGalectin 3HumansMCF-7 CellsGalectin 3Magnetite Nanoparticlesendosomesmagnetic nanoparticlesmembrane damageorganelle

Identifiers

PMID39756866
PMCPMC12702682

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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 OpenQuestion graph.