Evidence map›Paper›PMID 32467514›Full record

ArticleNeuroreport2020

Akt and Src mediate the photocrosslinked fibroin-induced neural differentiation.

Anastasia M Moysenovich, Viktor V Tatarskiy, Margarita A Yastrebova, Ivan V Bessonov, Anastasia Yu Arkhipova, Andrey S Kolosov, Lyubov I Davydova, Alvina I Khamidullina, Vladimir G Bogush, Vladimir G Debabov and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Neuroreport, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
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

13 authors at 5 institutions in 4 countries.

Anastasia M MoysenovichBiological Faculty, Lomonosov Moscow State University.
Viktor V TatarskiyLaboratory of Tumor Cell Death, Blokhin National Medical Center of Oncology.
Margarita A YastrebovaLaboratory of Molecular Oncobiology, Institute of Gene Biology, Russian Academy of Sciences.
Ivan V BessonovBiological Faculty, Lomonosov Moscow State University.
Anastasia Yu ArkhipovaBiological Faculty, Lomonosov Moscow State University.
Andrey S KolosovBiological Faculty, Lomonosov Moscow State University.
Lyubov I DavydovaNRC «Kurchatov Institute» - GOSNIIGENETIKA, Moscow, Russia.
Alvina I KhamidullinaLaboratory of Molecular Oncobiology, Institute of Gene Biology, Russian Academy of Sciences.
Vladimir G BogushNRC «Kurchatov Institute» - GOSNIIGENETIKA, Moscow, Russia.
Vladimir G DebabovNRC «Kurchatov Institute» - GOSNIIGENETIKA, Moscow, Russia.
Konstantin V ShaitanBiological Faculty, Lomonosov Moscow State University.
Alexander A ShtilLaboratory of Tumor Cell Death, Blokhin National Medical Center of Oncology.
Mikhail M MoisenovichBiological Faculty, Lomonosov Moscow State University.
Moscow State University · TJInstitute of Gene Biology · RUKurchatov Institute · RULomonosov Moscow State University · RUNational University of Science and Technology · ZW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neural transplantation is a promising modality for treatment of neurodegenerative diseases, traumatic brain injury and stroke. Biocompatible scaffolds with optimized properties improve the survival of transplanted neural cells and differentiation of progenitor cells into the desired types of neurons. Silk fibroin is a biocompatible material for tissue engineering. Here, we describe thin-film scaffolds based on photocrosslinked methacrylated silk fibroin (FBMA). These scaffolds exhibit an increased mechanical stiffness and improved water stability. Photocrosslinking of fibroin increased its rigidity from 25 to 480 kPa and the contact angle from 59.7 to 70.8, the properties important for differentiation of neural cells. Differentiation of SH-SY5Y neuroblastoma cells on FBMA increased the length of neurites as well as the levels of neural differentiation markers MAP2 and βIII-tubulin. Growth of SH-SY5Y cells on the unmodified fibroin and FBMA substrates led to a spontaneous phosphorylation of Src and Akt protein kinases critical for neuronal differentiation; this effect was paralleled by neural cell adhesion molecule elevation. Thus, FBMA is an easily manufactured, cytocompatible material with improved and sustainable properties applicable for neural tissue engineering.

Indexed as

Cell DifferentiationTissue ScaffoldsBiocompatible MaterialsCell Line, TumorCells, CulturedFibroinsHumansNeuronsProto-Oncogene Proteins c-aktProto-Oncogene Proteins pp60(c-src)Biocompatible MaterialsFibroinsProto-Oncogene Proteins c-aktProto-Oncogene Proteins pp60(c-src)

Identifiers

PMID32467514
PMCPMC7289124
OpenAlexW3030363478

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.