Evidence map›Paper›PMID 29354032›Full record

ArticleFrontiers in cellular neuroscience2017

Proteomic Dissection of Nanotopography-Sensitive Mechanotransductive Signaling Hubs that Foster Neuronal Differentiation in PC12 Cells.

Elisa Maffioli, Carsten Schulte, Simona Nonnis, Francesca Grassi Scalvini, Claudio Piazzoni, Cristina Lenardi, Armando Negri, Paolo Milani, Gabriella Tedeschi

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 32 citations in OpenAlex.

  1. Microfluidic Systems for Neural Cell Studies.Bioengineering (Basel, Switzerland) · 2023
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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

9 authors at 2 institutions in 1 country.

Elisa MaffioliDepartment of Veterinary Medicine, Università degli Studi di Milano, Milan, Italy.
Carsten SchulteCentre for Nanostructured Materials and Interfaces, Università degli Studi di Milano, Milan, Italy.
Simona NonnisDepartment of Veterinary Medicine, Università degli Studi di Milano, Milan, Italy.
Francesca Grassi ScalviniDepartment of Veterinary Medicine, Università degli Studi di Milano, Milan, Italy.
Claudio PiazzoniCentre for Nanostructured Materials and Interfaces, Università degli Studi di Milano, Milan, Italy.
Cristina LenardiCentre for Nanostructured Materials and Interfaces, Università degli Studi di Milano, Milan, Italy.
Armando NegriDepartment of Veterinary Medicine, Università degli Studi di Milano, Milan, Italy.
Paolo MilaniCentre for Nanostructured Materials and Interfaces, Università degli Studi di Milano, Milan, Italy.
Gabriella TedeschiDepartment of Veterinary Medicine, Università degli Studi di Milano, Milan, Italy.
University of Milan · ITFondazione Filarete · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuronal cells are competent in precisely sensing nanotopographical features of their microenvironment. The perceived microenvironmental information will be "interpreted" by mechanotransductive processes and impacts on neuronal functioning and differentiation. Attempts to influence neuronal differentiation by engineering substrates that mimic appropriate extracellular matrix (ECM) topographies are hampered by the fact that profound details of mechanosensing/-transduction complexity remain elusive. Introducing omics methods into these biomaterial approaches has the potential to provide a deeper insight into the molecular processes and signaling cascades underlying mechanosensing/-transduction but their exigence in cellular material is often opposed by technical limitations of major substrate top-down fabrication methods. Supersonic cluster beam deposition (SCBD) allows instead the bottom-up fabrication of nanostructured substrates over large areas characterized by a quantitatively controllable ECM-like nanoroughness that has been recently shown to foster neuron differentiation and maturation. Exploiting this capacity of SCBD, we challenged mechanosensing/-transduction and differentiative behavior of neuron-like PC12 cells with diverse nanotopographies and/or changes of their biomechanical status, and analyzed their phosphoproteomic profiles in these settings. Versatile proteins that can be associated to significant processes along the mechanotransductive signal sequence, i.e., cell/cell interaction, glycocalyx and ECM, membrane/f-actin linkage and integrin activation, cell/substrate interaction, integrin adhesion complex, actomyosin organization/cellular mechanics, nuclear organization, and transcriptional regulation, were affected. The phosphoproteomic data suggested furthermore an involvement of ILK, mTOR, Wnt, and calcium signaling in these nanotopography- and/or cell mechanics-related processes. Altogether, potential nanotopography-sensitive mechanotransductive signaling hubs participating in neuronal differentiation were dissected.

Indexed as

biomaterialbiophysicscell adhesionintegrin signalingmechanotransductionneuronal differentiationquantitative shot gun proteomics

Identifiers

PMID29354032
PMCPMC5758595
OpenAlexW2781738207

What OpenQuestion holds

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LicenceCC BY
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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.