Evidence map›Paper›PMID 42453052›Full record

ArticleACS nano2026

Modulation of Cilia Motility by Vortex-Ultrasound-Induced Shear Stress.

Thi-Nhan Phan, Hsien-Chu Wang, Ching-Hsiang Fan, Chung-Han Huang, Yin Fang, Yucheng Luo, Zhichao Ma, I-Hsuan Lin, Won-Jing Wang, Yu-Chun Lin and 1 more

Abstract read
In one paragraph

Article in ACS nano, 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

11 authors.

Thi-Nhan PhanDepartment of Biomedical Engineering and Environmental Sciences, National Tsing Hua University, Hsinchu30013, Taiwan.ORCID 0009-0007-4898-9259
Hsien-Chu WangInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu30013, Taiwan.
Ching-Hsiang FanDepartment of Biomedical Engineering, National Cheng Kung University, Tainan701401, Taiwan.
Chung-Han HuangDepartment of Biomedical Engineering and Environmental Sciences, National Tsing Hua University, Hsinchu30013, Taiwan.
Yin FangInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu30013, Taiwan.
Yucheng LuoInstitute of Medical Robotics, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai200030, China.
Zhichao MaInstitute of Medical Robotics, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai200030, China.
I-Hsuan LinInstitute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Taipei300093, Taiwan.
Won-Jing WangInstitute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Taipei300093, Taiwan.
Yu-Chun LinInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu30013, Taiwan.ORCID 0000-0002-9629-7560
Chih-Kuang YehDepartment of Biomedical Engineering and Environmental Sciences, National Tsing Hua University, Hsinchu30013, Taiwan.ORCID 0000-0002-2880-6327

Funding

National Science and Technology Council 112-2628-B-A49-009-MY3National Science and Technology Council 113-2221-E-007-022-MY3National Science and Technology Council 113-2320-B-A49-018-MY3National Science and Technology Council 113-2636-E-006-002National Science and Technology Council 114-2221-E-007-043-MY3National Science and Technology Council 114-2321-B-002-028National Science and Technology Council 114-2470-B-007-001National Science and Technology Council 114-2628-B-007-001National Science and Technology Council 1142628-E-006 -004 -MY4
6 · The paper itself

Abstract

The precise and noninvasive modulation of primary ciliary mechanotransduction remains a significant challenge in cell biology. Current approaches induce cilia motility─including microfluidic flow, optical tweezers, magnetic actuation, and genetic or optogenetic techniques─are constrained by low spatiotemporal precision and poor suitability for in vivo applications. Here, we present a noninvasive approach using vortex ultrasound (VUS) to generate localized shear stress via helical acoustic streaming. Using a 3.5 MHz transducer, VUS-generated shear stresses were approximately 5-fold higher than for conventional focused ultrasound, inducing cilia deflections of up to 80°. This mechanical stimulation triggered cilia-dependent calcium influx via ciliary ion channels, including transient receptor potential vanilloid 4 (TRPV4) and transient receptor potential polycystin 2 (TRPP2), demonstrating the direct activation of primary ciliary mechanotransduction by VUS-induced shear stress. These findings indicate VUS is a powerful tool for ciliary mechanobiology that can offer a scalable physical modality for investigating and manipulating cilia-associated signaling pathways in intact biological systems.

Indexed as

CiliaStress, MechanicalUltrasonic WavesAnimalsCalciumMechanotransduction, CellularMiceShear StrengthTRPP Cation ChannelsTRPV Cation ChannelsCalciumTRPP Cation ChannelsTRPV Cation Channelscilia motilityneuromodulationshear stressultrasoundvortex ultrasound

Identifiers

PMID42453052
PMCPMC13421962

What Socratic holds

Textmetadata
LicenceCC BY
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.