Evidence map›Paper›PMID 41526365›Full record

ArticleNature communications2026

Living sensor display implanted on skin for long-term biomarker monitoring.

Jun Sawayama, Makoto Takeo, Yuki Takayama, Miki Takase, Hoshimi Aoyagi, Aki Takimoto, Saki Mizutani, Maiko Onuki, Satoshi Ikeo, Shogo Nagata and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Jun SawayamaInstitute of Industrial Science, The University of Tokyo, Tokyo, Meguro-ku, Japan.ORCID 0009-0004-9871-8252
Makoto TakeoRIKEN Center for Biosystems Dynamics Research (BDR), Hyogo, Kobe, Japan.
Yuki TakayamaInstitute of Industrial Science, The University of Tokyo, Tokyo, Meguro-ku, Japan.
Miki TakaseRIKEN Center for Biosystems Dynamics Research (BDR), Hyogo, Kobe, Japan.
Hoshimi AoyagiInstitute of Industrial Science, The University of Tokyo, Tokyo, Meguro-ku, Japan.
Aki TakimotoInstitute of Industrial Science, The University of Tokyo, Tokyo, Meguro-ku, Japan.
Saki MizutaniInstitute of Industrial Science, The University of Tokyo, Tokyo, Meguro-ku, Japan.
Maiko OnukiInstitute of Industrial Science, The University of Tokyo, Tokyo, Meguro-ku, Japan.
Satoshi IkeoInstitute of Industrial Science, The University of Tokyo, Tokyo, Meguro-ku, Japan.ORCID 0000-0002-0959-4779
Shogo NagataInstitute of Industrial Science, The University of Tokyo, Tokyo, Meguro-ku, Japan.
Miho OgawaRIKEN Center for Biosystems Dynamics Research (BDR), Hyogo, Kobe, Japan.
Koji YanoCanon Medical Systems Co., Kanagawa, Kawasaki, Japan.
Takashi TsujiRIKEN Center for Biosystems Dynamics Research (BDR), Hyogo, Kobe, Japan.ORCID 0000-0002-2230-8052
Shoji TakeuchiInstitute of Industrial Science, The University of Tokyo, Tokyo, Meguro-ku, Japan.ORCID 0000-0001-6946-0409
Hiroyuki FujitaCanon Medical Systems Co., Kanagawa, Kawasaki, Japan. hfujita@tcu.ac.jp.

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) JP21H05013MEXT | Japan Society for the Promotion of Science (JSPS) JP22H00284
6 · The paper itself

Abstract

This study introduces an approach to biomarker monitoring through the development of a "Living Sensor Display" implanted on the skin, designed for long-term, continuous tracking of biomarkers, such as inflammatory cytokines. By leveraging the natural high selectivity and sensitivity of keratinocyte stem cells (KSCs) to environmental stimuli, we genetically engineered these cells to express fluorescent proteins in response to specific biomarker signals, specifically TNF-α signalling. This innovation allows for the real-time, non-invasive observation, with the only invasive step being the initial implantation, of biomarker levels directly from the skin surface. We constructed tissue-engineered skin with genetically modified KSCs and transplanted it onto mice, where it successfully engrafted long-term, matured to mimic human skin structures, and responsively indicated the presence of TNF-α through visible fluorescence. This living sensor could repeatedly detect inflammatory responses induced by TNF-α and lipopolysaccharides, highlighting its potential for monitoring various physiological and pathological processes over extended periods. This Living sensor display holds promise for advancing health monitoring and disease prevention strategies by enabling continuous, sensitive, and specific in vivo biomarker tracking.

Indexed as

BiomarkersBiosensing TechniquesSkinAnimalsHumansKeratinocytesMiceStem CellsTissue EngineeringTumor Necrosis Factor-alphaBiomarkersTumor Necrosis Factor-alpha

Identifiers

PMID41526365
PMCPMC12796179

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.