# Mechanical stress-mediated immune and inflammatory regulation: a bibliometric and visualization analysis of mechanoimmunology based on two databases

**Authors:** Jiayuecheng Pang, Yicheng Ma, Hongchao Huang, Jiqing Ma, Yongjun Zheng, Shichu Xiao, Zhaofan Xia

PMC · DOI: 10.3389/fmed.2025.1698177 · 2025-11-06

## TL;DR

This paper analyzes the growing field of mechanoimmunology, showing how mechanical stress influences immune and inflammatory responses, and highlights recent research trends and key targets.

## Contribution

The study provides a comprehensive bibliometric and visual analysis of mechanoimmunology research trends and emerging topics.

## Key findings

- The United States and China are leading research hubs in mechanoimmunology.
- Research on mechanoimmunology has surged since 2021, with new clusters like 'T cells' and 'macrophage polarization' emerging.
- Piezo1 and YAP/TAZ are identified as key mechanosensitive targets in immune-inflammatory modulation.

## Abstract

With advances in detection technologies and the trend of interdisciplinary integration, mechanical stress in biomechanics has been shown to exert broad effects on organisms. It influences multiple cellular processes, including proliferation, migration, and differentiation, and also plays a critical regulatory role in both immune cell function and the organismal immune-inflammatory response. Thus, an emerging interdisciplinary field—mechanoimmunology—has emerged. However, the specific mechanisms underlying this field remain incompletely elucidated. Herein, this study aims to identify the latest research hotspots and provide a thorough analysis of the current research status in this domain.

A total of 1,901 articles were retrieved from the Web of Science Core Collection (WOSCC) and 2,954 articles from Scopus. These selected articles were imported into bibliometric analysis software for preliminary data processing, followed by further visual analysis using multiple graphing tools. Finally, specific analyses were conducted based on various categories, including journals, authors, geographical distribution, citations, and keywords.

The United States and China are the two leading research hubs in this field, with the University of California System currently standing as the most influential institution. A surge in research on mechanoimmunology has been observed since 2021. During the “Research Explosion Phase” post-2021, several new keyword clusters emerged, including “T cells,” “macrophage polarization,” and “ion channels,” alongside clusters related to emerging fields such as “wound healing,” “gut microbiota,” and “bone remodeling.” The mechanosensitive ion channel protein Piezo1 and the YAP/TAZ transcription complex in the Hippo pathway have emerged as key targets in recent studies.

This study identifies the ongoing research surge in the field of mechanoimmunology while comprehensively delineating the current research landscape. Additionally, through keyword clustering across different phases, it uncovers the latest research hotspots and potential future research directions focused on novel mechanosensitive targets for immune-inflammatory modulation. This work provides a clear research roadmap for investigators in the field, offering insights into future research possibilities.

## Linked entities

- **Proteins:** PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)), YAP1 (Yes1 associated transcriptional regulator), TAFAZZIN (tafazzin, phospholipid-lysophospholipid transacylase)

## Full-text entities

- **Genes:** YAP1 (Yes1 associated transcriptional regulator) [NCBI Gene 10413] {aka COB1, YAP, YAP-1, YAP2, YAP65, YKI}, PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)) [NCBI Gene 9780] {aka DHS, ER, FAM38A, LMPH3, LMPHM6, Mib}, TAFAZZIN (tafazzin, phospholipid-lysophospholipid transacylase) [NCBI Gene 6901] {aka BTHS, CMD3A, EFE, EFE2, G4.5, LVNCX}
- **Diseases:** inflammatory (MESH:D007249)

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12631210/full.md

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Source: https://tomesphere.com/paper/PMC12631210