Evidence map›Paper›PMID 40981678›Full record

ArticleCurrent protocols2025

Isolation, Extraction, and Analysis of Cells After Confined Migration.

Xu Gao, Yixuan Li, Jia Wen Nicole Lee, Jianxuan Zhou, Vaishnavi Rangaraj, Avery Rui Sun, Jennifer L Young, Andrew W Holle

Abstract read
In one paragraph

Article in Current protocols, 2025. 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. Article
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

8 authors.

Xu GaoDepartment of Biomedical Engineering, College of Design and Engineering, National University of Singapore, Singapore.
Yixuan LiMechanobiology Institute, National University of Singapore, Singapore.
Jia Wen Nicole LeeMechanobiology Institute, National University of Singapore, Singapore.
Jianxuan ZhouDepartment of Biomedical Engineering, College of Design and Engineering, National University of Singapore, Singapore.
Vaishnavi RangarajDepartment of Biomedical Engineering, College of Design and Engineering, National University of Singapore, Singapore.
Avery Rui SunDepartment of Biomedical Engineering, College of Design and Engineering, National University of Singapore, Singapore.
Jennifer L YoungDepartment of Biomedical Engineering, College of Design and Engineering, National University of Singapore, Singapore.
Andrew W HolleDepartment of Biomedical Engineering, College of Design and Engineering, National University of Singapore, Singapore.ORCID https://orcid.org/0000-0002-7206-0964

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell migration through confined microenvironments is a critical biological process that underlies numerous physiological and pathological events, including immune cell trafficking, tissue morphogenesis, and cancer metastasis. Although polydimethylsiloxane-based microchannel devices have enabled detailed studies of confined migration, the efficient collection of cells post-migration for downstream molecular analyses remains a major challenge. Existing approaches often rely on harsh mechanical dissociation that compromises cell viability and integrity and do not permit in situ collection of cell lysates. To overcome these limitations, we have developed the Trap-based Recovery After Permeation (TRAP) chip, a pump-free microfluidic platform that integrates controlled confined migration with efficient post-migration cell or lysate collection. The TRAP chip incorporates microchannel arrays terminating in a precisely engineered trap region that enables gentle recovery of cells or cellular components without exposing them to high shear forces or requiring large buffer volumes. This innovation ensures the viability of recovered cells and expands the applicability of confined migration assays beyond imaging-based studies. We demonstrate that the TRAP chip facilitates the extraction of post-confinement cells for mechanical characterization, including measurement of Young's modulus, as well as the isolation of proteins and RNA suitable for downstream assays such as western blot and qPCR. The TRAP chip thus represents a significant advancement in microfluidic technologies, offering a robust, reproducible, and minimally invasive approach for studying the mechanobiology of confined migration, with broad potential for applications in basic research, cellular engineering, and translational studies where cell behavior under physical confinement is of critical importance. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Fabrication of TRAP and control chips Basic Protocol 2: Cell seeding and live cell isolation from TRAP chips Alternate Protocol: Biomolecular extraction from TRAP chips.

Indexed as

Cell MovementCell SeparationMicrofluidic Analytical TechniquesHumansLab-On-A-Chip Devicescell collectioncell migrationconfined migrationmicrofluidic devicemolecular analysis

Identifiers

PMID40981678
PMCPMC12452805

What OpenQuestion holds

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LicenceCC BY-NC
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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.