Evidence map›Paper›PMID 30282987›Full record

ArticleNature communications2018

Bi-directional cell-pericellular matrix interactions direct stem cell fate.

Silvia A Ferreira, Meghna S Motwani, Peter A Faull, Alexis J Seymour, Tracy T L Yu, Marjan Enayati, Dheraj K Taheem, Christoph Salzlechner, Tabasom Haghighi, Ewa M Kania and 12 more

Erratum issuedAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing 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

67 citing papers in PubMed.

  1. Nascent Extracellular Matrix Converts Biomaterial Cues into Cell Fate Decisions.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Silvia A FerreiraCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.ORCID http://orcid.org/0000-0001-7837-3040
Meghna S MotwaniCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Peter A FaullProtein Analysis and Proteomics Platform, The Francis Crick Institute, London, NW1 1AT, UK.
Alexis J SeymourCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Tracy T L YuCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Marjan EnayatiCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Dheraj K TaheemCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Christoph SalzlechnerCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Tabasom HaghighiCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Ewa M KaniaCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Oommen P OommenBioengineering and Nanomedicine Lab, Faculty of Biomedical Sciences and Engineering, Tampere University of Technology and BioMediTech Institute, 33720, Tampere, Finland.ORCID http://orcid.org/0000-0003-2768-0133
Tarek AhmedBiomaterials and Tissue Engineering, Eastman Dental Institute, University College London, London, WC1X 8LD, UK.
Sandra LoaizaCancer Cell Protein Metabolism Group, Department of Medicine, Imperial College London, London, W12 0NN, UK.
Katarzyna ParzychCancer Cell Protein Metabolism Group, Department of Medicine, Imperial College London, London, W12 0NN, UK.
Francesco DazziDepartment of Haemato-Oncology, Rayne Institute, King's College London, London, SE5 9NU, UK.
Oommen P VargheseDepartment of Chemistry, Ångström Laboratory, Science for Life Laboratory, Uppsala University, SE-75121, Uppsala, Sweden.
Frederic FestyTissue Engineering and Biophotonics, King's College London, London, SE1 9RT, UK.
Agamemnon E GrigoriadisCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Holger W AunerCancer Cell Protein Metabolism Group, Department of Medicine, Imperial College London, London, W12 0NN, UK.ORCID http://orcid.org/0000-0003-4040-0642
Ambrosius P SnijdersProtein Analysis and Proteomics Platform, The Francis Crick Institute, London, NW1 1AT, UK.ORCID http://orcid.org/0000-0002-5416-8592
Laurent BozecBiomaterials and Tissue Engineering, Eastman Dental Institute, University College London, London, WC1X 8LD, UK.
Eileen GentlemanCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK. eileen.gentleman@kcl.ac.uk.ORCID http://orcid.org/0000-0003-0447-5137

Funding

Cancer Research UK 15448Wellcome Trust FC001999
6 · The paper itself

Abstract

Modifiable hydrogels have revealed tremendous insight into how physical characteristics of cells' 3D environment drive stem cell lineage specification. However, in native tissues, cells do not passively receive signals from their niche. Instead they actively probe and modify their pericellular space to suit their needs, yet the dynamics of cells' reciprocal interactions with their pericellular environment when encapsulated within hydrogels remains relatively unexplored. Here, we show that human bone marrow stromal cells (hMSC) encapsulated within hyaluronic acid-based hydrogels modify their surroundings by synthesizing, secreting and arranging proteins pericellularly or by degrading the hydrogel. hMSC's interactions with this local environment have a role in regulating hMSC fate, with a secreted proteinaceous pericellular matrix associated with adipogenesis, and degradation with osteogenesis. Our observations suggest that hMSC participate in a bi-directional interplay between the properties of their 3D milieu and their own secreted pericellular matrix, and that this combination of interactions drives fate.

Indexed as

Cell CommunicationCell LineageAmidesCell-Matrix JunctionsHumansHydrogel, Polyethylene Glycol DimethacrylateMesenchymal Stem CellsPaclitaxelPyridinesStem CellsAmidesHydrogel, Polyethylene Glycol DimethacrylatePaclitaxelPyridinesY 27632

Identifiers

PMID30282987
PMCPMC6170409

What OpenQuestion holds

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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 OpenQuestion graph.