Evidence map›Paper›PMID 42099638›Full record

SynthesisFrontiers in immunology2026

Macrophage mechanobiology: from sensing to disease.

Mario D'Ambrosio, Khaled Warasnhe, Mohamed H Eldesouki, Vikram Joshi, Arthur Beyder, Gianluca Cipriani

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in immunology, 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

6 authors.

Mario D'AmbrosioEnteric Neuroscience Program (ENSP), Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.
Khaled WarasnheEnteric Neuroscience Program (ENSP), Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.
Mohamed H EldesoukiEnteric Neuroscience Program (ENSP), Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.
Vikram JoshiEnteric Neuroscience Program (ENSP), Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.
Arthur BeyderEnteric Neuroscience Program (ENSP), Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.
Gianluca CiprianiEnteric Neuroscience Program (ENSP), Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI Samar Ibrahim · 2009 to 2026
$22.2M
Pathophysiology of Diabetic GastroparesisR01DK127992 · NIDDK · MAYO CLINIC ROCHESTER · PI FARRUGIA, GIANRICO, GROVER, MADHUSUDAN · 2021 to 2024
$2.2M
Role of Muscularis Macrophages in the Enteric Nervous SystemR01DK129297 · NIDDK · MAYO CLINIC ROCHESTER · PI Gianluca Cipriani · 2022 to 2026
$1.9M
NIDDK NIH HHS P30 DK084567NIDDK NIH HHS R01 DK127992NIDDK NIH HHS R01 DK129297
6 · The paper itself

Abstract

Objective: Macrophages are highly plastic immune cells that maintain tissue homeostasis through their roles in immune surveillance, repair, and remodeling. Emerging evidence reveals that macrophages, residing in tissues with widely varying stiffness, are profoundly influenced by the mechanical properties of their microenvironment. Methods: Relevant publications on macrophage mechanoregulation published up to January 2026 were identified through systematic searches of PubMed, EMBASE, and Web of Science using combinations of keywords related to macrophages, mechanosensing, mechanotransduction, and mechanical stimuli (e.g., stiffness, stretch, and shear stress). Articles were screened based on relevance to macrophage biology and mechanistic insights. Results: Mechanical cues are sensed through mechanosensors such as Piezo1, TRPV4, and integrins, which integrate these signals to regulate immune surveillance, inflammation, tissue repair, and remodeling. Dysregulation of these pathways contributes to the pathogenesis of multiple diseases, including fibrosis, atherosclerosis, and neurodegeneration. Conclusion: Macrophage mechanobiology represents a critical regulatory axis in tissue homeostasis and disease. Targeting mechanosensing pathways offers promising therapeutic opportunities to modulate inflammation and enhance tissue regeneration.

Indexed as

MacrophagesMechanotransduction, CellularAnimalsCellular MicroenvironmentHumansInflammationinflammationmacrophagemechanosensationmechanotransductionpolarizationstiffness

Identifiers

PMID42099638
PMCPMC13144072

What OpenQuestion holds

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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.