Evidence map›Paper›PMID 42843976›Full record

ArticleLife science alliance2026

Dysferlin promotes inflammatory macrophage responses and modulates Ca

Kana Tominaga, Naoomi Tominaga

Abstract read
In one paragraph

Article in Life science alliance, 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

2 authors.

Kana TominagaDivision of Neuropsychiatry, Department of Neuroscience, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan kanat@yamaguchi-u.ac.jp.ORCID https://orcid.org/0000-0001-5136-5091
Naoomi TominagaDivision of Clinical Laboratory Sciences, Department of Nursing and Laboratory Science, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.ORCID https://orcid.org/0000-0003-4368-6586

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophage differentiation and activation shape tissue homeostasis and regeneration. Dysferlin (DYSF) is best known for its role in membrane repair in skeletal muscle, but its function in immune cells remains poorly understood. Here, we identify DYSF as a regulator of inflammatory macrophage-associated activation. DYSF expression increased during monocyte-to-macrophage differentiation. Gain- and loss-of-function analyses revealed that DYSF promoted inflammatory macrophage-associated responses, including cytokine production and migration. DYSF also enhanced Ca

Indexed as

CalciumDysferlinInflammationMacrophagesSTAT1 Transcription FactorAnimalsCell DifferentiationHumansMiceMuscle DevelopmentMuscle, SkeletalSignal TransductionCalciumDysferlinDYSF protein, humanDysf protein, mouseSTAT1 protein, humanStat1 protein, mouseSTAT1 Transcription Factor

Identifiers

PMID42843976
PMCPMC13646497

What Socratic holds

Textmetadata
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 Socratic graph.