Evidence map›Paper›PMID 29403036›Full record

ArticleNature cell biology2018

Non-invasive perturbations of intracellular flow reveal physical principles of cell organization.

Matthäus Mittasch, Peter Gross, Michael Nestler, Anatol W Fritsch, Christiane Iserman, Mrityunjoy Kar, Matthias Munder, Axel Voigt, Simon Alberti, Stephan W Grill and 1 more

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In one paragraph

Article in Nature cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
32.1field-weighted citation impact, top 1% of its field
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

68 citing papers in PubMed, 147 citations in OpenAlex.

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  9. A mechanism for MEX-5-driven disassembly of PGL-3/RNA condensates in vitro.Proceedings of the National Academy of Sciences of the United States of America · 2025
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8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Matthäus MittaschMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Peter GrossBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
Michael NestlerDepartment of Mathematics, Technische Universität Dresden, Dresden, Germany.
Anatol W FritschMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.ORCID http://orcid.org/0000-0003-0986-7068
Christiane IsermanMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Mrityunjoy KarMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Matthias MunderMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Axel VoigtCenter for Systems Biology, Dresden, Germany.
Simon AlbertiMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Stephan W GrillCenter for Systems Biology, Dresden, Germany.
Moritz KreysingMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany. kreysing@mpi-cbg.de.ORCID http://orcid.org/0000-0001-7432-3871
Center for Systems Biology Dresden · DEMax Planck Institute of Molecular Cell Biology and Genetics · DETechnische Universität Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in cell biology enable precise molecular perturbations. The spatiotemporal organization of cells and organisms, however, also depends on physical processes such as diffusion or cytoplasmic flows, and strategies to perturb physical transport inside cells are not yet available. Here, we demonstrate focused-light-induced cytoplasmic streaming (FLUCS). FLUCS is local, directional, dynamic, probe-free, physiological, and is even applicable through rigid egg shells or cell walls. We explain FLUCS via time-dependent modelling of thermoviscous flows. Using FLUCS, we demonstrate that cytoplasmic flows drive partitioning-defective protein (PAR) polarization in Caenorhabditis elegans zygotes, and that cortical flows are sufficient to transport PAR domains and invert PAR polarity. In addition, we find that asymmetric cell division is a binary decision based on gradually varying PAR polarization states. Furthermore, the use of FLUCS for active microrheology revealed a metabolically induced fluid-to-solid transition of the yeast cytoplasm. Our findings establish how a wide range of transport-dependent models of cellular organization become testable by FLUCS.

Indexed as

Cytoplasmic StreamingAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCaenorhabditis elegans ProteinsCell Cycle ProteinsCell PolarityInfrared RaysLasersModels, BiologicalPhenotypeRheologySaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSingle-Cell AnalysisTime FactorsCaenorhabditis elegans ProteinsCell Cycle ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID29403036
OpenAlexW2790048502

What OpenQuestion holds

Textmetadata
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.