Evidence map›Paper›PMID 42724607›Full record

ArticleMaterials today. Bio2026

Engineering migrasome-inspired extracellular vesicles through temperature stimuli on thermoresponsive substrate for retraction fiber formation and hypoosmotic vesiculation.

Koki Yoshikawa, Shogo Saito, Mina Okochi

Abstract read
In one paragraph

Article in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Koki YoshikawaDepartment of Chemical Science and Engineering, Institute of Science Tokyo, 2-12-1, O-okayama, Meguro-ku, Tokyo, 152-8550, Japan.
Shogo SaitoDepartment of Chemical Science and Engineering, Institute of Science Tokyo, 2-12-1, O-okayama, Meguro-ku, Tokyo, 152-8550, Japan.
Mina OkochiDepartment of Chemical Science and Engineering, Institute of Science Tokyo, 2-12-1, O-okayama, Meguro-ku, Tokyo, 152-8550, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Migrasomes, recently identified extracellular vesicles, play critical roles in physiological processes such as tissue remodeling and intercellular communication. However, their generally low and cell-type-dependent biogenesis limits their broader applications. Here, a simple and scalable method for producing migrasome-inspired vesicles, termed osmotically-induced migrasome-like vesicles (OsMigs), through temperature stimuli-induced retraction fiber on thermoresponsive polymer-modified substrates and hypoosmotic vesiculation was developed. A two-step cooling treatment of 4 °C and 20 °C on the poly (N-isopropylacrylamide)-modified substrate coincidently led to the appearance of retraction fibers. This approach reproducibly achieved more than an order-of-magnitude increase in vesicle yield compared to migrasome biogenesis in normal human dermal fibroblasts, and is broadly applicable to multiple adherent cell types, including even those that do not naturally form migrasomes. OsMigs are enriched in migrasome-associated markers, including tetraspanin-4, integrin α5, and cholesterol, and encapsulate bioactive cytokines. Functionally, OsMigs significantly promote fibroblast migration and angiogenesis

Indexed as

Extracellular vesiclesMigrasomePoly-N-isopropylacrylamideWound healing

Identifiers

PMID42724607
PMCPMC13560315

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.