Evidence map›Paper›PMID 27613598›Full record

ArticleStem cell research & therapy2016

Two-photon polymerized "nichoid" substrates maintain function of pluripotent stem cells when expanded under feeder-free conditions.

Michele M Nava, Alessio Piuma, Marina Figliuzzi, Irene Cattaneo, Barbara Bonandrini, Tommaso Zandrini, Giulio Cerullo, Roberto Osellame, Andrea Remuzzi, Manuela T Raimondi

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
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  5. Two-Photon Polymerization: Fundamentals, Materials, and Chemical Modification Strategies.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
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  16. Tissue engineering and regenerative medicine strategies for the female breast.Journal of tissue engineering and regenerative medicine · 2020
    Review
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  18. 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

10 authors.

Michele M NavaDepartment of Chemistry, Materials and Chemical Engineering "Giulio Natta", Politecnico di Milano, 32, piazza Leonardo da Vinci, 20133, Milan, Italy. michele.nava@polimi.it.
Alessio PiumaDepartment of Chemistry, Materials and Chemical Engineering "Giulio Natta", Politecnico di Milano, 32, piazza Leonardo da Vinci, 20133, Milan, Italy.
Marina FigliuzziIRCCS Istituto di Ricerche Farmacologiche "Mario Negri", Bergamo, Italy.
Irene CattaneoIRCCS Istituto di Ricerche Farmacologiche "Mario Negri", Bergamo, Italy.
Barbara BonandriniIRCCS Istituto di Ricerche Farmacologiche "Mario Negri", Bergamo, Italy.
Tommaso ZandriniIstituto di Fotonica e Nanotecnologie (IFN) - CNR and Department of Physics, Politecnico di Milano, Milan, Italy.
Giulio CerulloIstituto di Fotonica e Nanotecnologie (IFN) - CNR and Department of Physics, Politecnico di Milano, Milan, Italy.
Roberto OsellameIstituto di Fotonica e Nanotecnologie (IFN) - CNR and Department of Physics, Politecnico di Milano, Milan, Italy.
Andrea RemuzziDepartment of Management, Information and Production Engineering, University of Bergamo, Dalmine, Italy.
Manuela T RaimondiDepartment of Chemistry, Materials and Chemical Engineering "Giulio Natta", Politecnico di Milano, 32, piazza Leonardo da Vinci, 20133, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe use of pluripotent cells in stem cell therapy has major limitations, mainly related to the high costs and risks of exogenous conditioning and the use of feeder layers during cell expansion passages.

methodsWe developed an innovative three-dimensional culture substrate made of "nichoid" microstructures, nanoengineered via two-photon laser polymerization. The nichoids limit the dimension of the adhering embryoid bodies during expansion, by counteracting cell migration between adjacent units of the substrate by its microarchitecture. We expanded mouse embryonic stem cells on the nichoid for 2 weeks. We compared the expression of pluripotency and differentiation markers induced in cells with that induced by flat substrates and by a culture layer made of kidney-derived extracellular matrix.

resultsThe nichoid was found to be the only substrate, among those tested, that maintained the expression of the OCT4 pluripotency marker switched on and, simultaneously, the expression of the differentiation markers GATA4 and α-SMA switched off. The nichoid promotes pluripotency maintenance of embryonic stem cells during expansion, in the absence of a feeder layer and exogenous conditioning factors, such as the leukocyte inhibitory factor.

conclusionsWe hypothesized that the nichoid microstructures induce a genetic reprogramming of cells by controlling their cytoskeletal tension. Further studies are necessary to understand the exact mechanism by which the physical constraint provided by the nichoid architecture is responsible for cell reprogramming. The nichoid may help elucidate mechanisms of pluripotency maintenance, while potentially cutting the costs and risks of both feed-conditioning and exogenous conditioning for industrial-scale expansion of stem cells.

Indexed as

AnimalsBiomarkersCell Culture TechniquesCell DifferentiationCell MovementCells, CulturedCellular ReprogrammingEmbryoid BodiesEmbryonic Stem CellsExtracellular MatrixFeeder CellsLasersMaleMicePluripotent Stem CellsRats, Sprague-DawleyBiomarkersEmbryonic stem cellsMechanobiologyNanofabricationPluripotencyScaffoldTwo-photon polymerization

Identifiers

PMID27613598
PMCPMC5016857

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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.