Evidence map›Paper›PMID 41748583›Full record

ArticleNature communications2026

Gear-like MOF microrobots for single cell mechanotransduction of microvilli.

Xiaoxia Liu, Yong Wang, Lin Lin, Ning Liu, Zihao Yang, Peng Wang, Xiaohui Yan, Jinhong Guo, Dongdong Jin, Xing Ma

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

10 authors.

Xiaoxia LiuSauvage Laboratory for Smart Materials, School of Integrated Circuits, Harbin Institute of Technology (Shenzhen), Shenzhen, China.
Yong WangKey Laboratory of Clinical Laboratory Diagnostics (Chinese Ministry of Education), College of Laboratory Medicine, Chongqing Medical University, Chongqing, China. wangyong@cqmu.edu.cn.
Lin LinState Key Laboratory of Molecular Vaccinology and Molecular Diagnostics & Center for Molecular Imaging and Translational Medicine, School of Public Health, Xiamen University, Xiamen, China.
Ning LiuSchool of Aerospace Engineering and Applied Mechanics, Tongji University, Shanghai, China.
Zihao YangSchool of Computing and Artificial Intelligence, Southwest Jiaotong University, Chengdu, China.
Peng WangSauvage Laboratory for Smart Materials, School of Integrated Circuits, Harbin Institute of Technology (Shenzhen), Shenzhen, China.
Xiaohui YanState Key Laboratory of Molecular Vaccinology and Molecular Diagnostics & Center for Molecular Imaging and Translational Medicine, School of Public Health, Xiamen University, Xiamen, China.ORCID http://orcid.org/0000-0001-6089-0664
Jinhong GuoKey Laboratory of Clinical Laboratory Diagnostics (Chinese Ministry of Education), College of Laboratory Medicine, Chongqing Medical University, Chongqing, China.ORCID http://orcid.org/0000-0003-2659-3150
Dongdong JinSauvage Laboratory for Smart Materials, School of Integrated Circuits, Harbin Institute of Technology (Shenzhen), Shenzhen, China. jindongdong@hit.edu.cn.ORCID http://orcid.org/0000-0003-4833-538X
Xing MaSauvage Laboratory for Smart Materials, School of Integrated Circuits, Harbin Institute of Technology (Shenzhen), Shenzhen, China. maxing@hit.edu.cn.ORCID http://orcid.org/0000-0002-2248-4806

Funding

China Postdoctoral Science Foundation 2024M763882National Natural Science Foundation of China (National Science Foundation of China) 82402730Shenzhen Science and Technology Innovation Commission KJZD20231023100302006Shenzhen Science and Technology Innovation Commission RCJC20231211090000001; GXWD20231129101105001
6 · The paper itself

Abstract

Cellular mechanotransduction, mediated by specialized structures such as microvilli, regulates processes ranging from tissue homeostasis to disease progression. Existing tools for microvilli-specific biomechanical intervention suffer from limited spatiotemporal precision and non-physiological constraints, restricting mechanistic studies and targeted therapies. Here, we develop a magnetically driven gear-like metal-organic framework microrobot (MOFbot) for programmable mechanical manipulation of single-cell microvilli. MOFbots are fabricated through epitaxial growth of heterogeneous MOF structures followed by deposition of Ni/Au nanofilms. Under a rotating magnetic field, they perform rolling and obstacle negotiation. Their rotating gear structure entangles microvilli, exerting quantified pulling forces via Förster resonance energy transfer and traction force microscopy. This mechanical stimulation triggers intracellular calcium influx and enhanced focal adhesion kinase phosphorylation, indicating mechanotransduction pathway activation. Consequently, rotating MOFbots increase membrane permeability, enabling on-demand transmembrane delivery of therapeutics into targeted single cells. This work establishes a targeted cellular mechanomodulation strategy and informs future micro/nanorobotic biomedical designs.

Indexed as

Mechanotransduction, CellularMicrovilliRoboticsSingle-Cell AnalysisAnimalsCalciumFluorescence Resonance Energy TransferFocal Adhesion Protein-Tyrosine KinasesGoldHumansNickelPhosphorylationCalciumFocal Adhesion Protein-Tyrosine KinasesGoldNickel

Identifiers

PMID41748583
PMCPMC13061913

What OpenQuestion holds

Textmetadata
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.