Evidence map›Paper›PMID 31069245›Full record

ArticleACS photonics2018

Visualizing Spatiotemporal Dynamics of Intercellular Mechanotransmission upon Wounding.

Pengzhi Wang, Jing Liang, Linda Z Shi, Yi Wang, Ping Zhang, Mingxing Ouyang, Daryl Preece, Qin Peng, Lunan Shao, Jason Fan and 5 more

Abstract read
In one paragraph

Article in ACS photonics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Recent developments in DNA-based mechanical nanodevices.Chemical communications (Cambridge, England) · 2022
    Review
  3. Article
  4. Article
  5. Article
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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

15 authors.

Pengzhi Wang *Department of Bioengineering, University of California, San Diego, La Jolla, California 92093, United States.ORCID 0000-0001-7474-9661
Jing Liang *Department of Chemical and Biomolecular Engineering and Carl R. Woese Institute for Genomic Biology.
Linda Z ShiInstitute of Engineering in Medicine, University of California, San Diego, La Jolla, California 92093, United States.
Yi WangDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.
Ping ZhangInstitute of Mechanobiology and Biomedical Engineering, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China.
Mingxing OuyangDepartment of Bioengineering, University of California, San Diego, La Jolla, California 92093, United States.
Daryl PreeceDepartment of NanoEngineering, University of California, San Diego, La Jolla, California 92093, United States.
Qin PengDepartment of Bioengineering, University of California, San Diego, La Jolla, California 92093, United States.
Lunan ShaoDepartment of Bioengineering, University of California, San Diego, La Jolla, California 92093, United States.
Jason FanInstitute of Engineering in Medicine, University of California, San Diego, La Jolla, California 92093, United States.
Jie SunDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.
Shawn S LiDepartment of Biochemistry, Schulich School of Medicine and Dentistry, Western University, London, Ontario Canada N6A 5C1.
Michael W BernsDepartment of Bioengineering, University of California, San Diego, La Jolla, California 92093, United States.
Huimin ZhaoDepartment of Chemical and Biomolecular Engineering and Carl R. Woese Institute for Genomic Biology.ORCID 0000-0002-9069-6739
Yingxiao WangDepartment of Bioengineering, University of California, San Diego, La Jolla, California 92093, United States.

Funding

Role of Spatiotemporal Epigenetic Dynamics in Regulating Endothelial Gene Expressions under FlowsR01HL121365 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHIEN, SHU, WANG, YINGXIAO · 2014 to 2025
$7.5M
Locus-specific Imaging of Dynamic Histone Methylations during ReprogrammingR01GM125379 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHIEN, SHU, WANG, YINGXIAO · 2017 to 2020
$2.4M
Multiplex FRET Imaging of Kinase-Epigenome Interregulations in Live Cancer CellsR33CA204704 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WANG, YINGXIAO · 2017 to 2019
$1.1M
Remote-Control Mechano-Genetics and Epigenetics for Live Cell ManipulationR01GM126016 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WANG, YINGXIAO · 2018 to 2020
$1.1M
Engineering Machinery Molecules to Visualize and Actuate ImmunotherapyR21CA209629 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WANG, YINGXIAO · 2017 to 2018
$371k
NCI NIH HHS R21 CA209629NCI NIH HHS R33 CA204704NHLBI NIH HHS R01 HL121365NIGMS NIH HHS R01 GM125379NIGMS NIH HHS R01 GM126016
6 · The paper itself

Abstract

During cell-to-cell communications, the interplay between physical and biochemical cues is essential for informational exchange and functional coordination, especially in multicellular organisms. However, it remains a challenge to visualize intercellular signaling dynamics in single live cells. Here, we report a photonic approach, based on laser microscissors and Förster resonance energy transfer (FRET) microscopy, to study intercellular signaling transmission. First, using our high-throughput screening platform, we developed a highly sensitive FRET-based biosensor (SCAGE) for Src kinase, a key regulator of intercellular interactions and signaling cascades. Notably, SCAGE showed a more than 40-fold sensitivity enhancement than the original biosensor in live mammalian cells. Next, upon local severance of physical intercellular connections by femtosecond laser pulses, SCAGE enabled the visualization of a transient Src activation across neighboring cells. Lastly, we found that this observed transient Src activation following the loss of cell-cell contacts depends on the passive structural support of cytoskeleton but not on the active actomyosin contractility. Hence, by precisely introducing local physical perturbations and directly visualizing spatiotemporal transmission of ensuing signaling events, our integrated approach could be broadly applied to mimic and investigate the wounding process at single-cell resolutions. This integrated approach with highly sensitive FRET-based biosensors provides a unique system to advance our in-depth understanding of molecular mechanisms underlying the physical-biochemical basis of intercellular coupling and wounding processes.

Indexed as

active actomyosin contractilitydirected evolutionFRET imaginghighly sensitive FRET-based biosensor SCAGEhigh-throughput screeninglaser-induced woundingpassive structural support of cytoskeletontransient Src activation

Identifiers

PMID31069245
PMCPMC6502247

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Registered trials

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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.