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

Title: Akt and Src mediate the photocrosslinked fibroin-induced neural differentiation.
Authors: Moysenovich, Anastasia M.; Tatarskiy, Viktor V.; Yastrebova, Margarita A.; Bessonov, Ivan V.; Arkhipova, Anastasia Yu; Kolosov, Andrey S.; Davydova, lyubov I.; Khamidullina, Alvina I.; Bogush, Vladimir G.; Debabov, Vladimir G.; Shaitan, Konstantin V.; Shtil, Alexander A.; Moisenovich, Mikhail M.
Source: NeuroReport ; volume 31, issue 10, page 770-775 ; ISSN 0959-4965
Publisher Information: Ovid Technologies (Wolters Kluwer Health)
Publication Year: 2020
Description: 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 o to 70.8 o , 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.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1097/wnr.0000000000001482
DOI: 10.1097/WNR.0000000000001482
Availability: https://doi.org/10.1097/wnr.0000000000001482; https://journals.lww.com/10.1097/WNR.0000000000001482
Rights: https://creativecommons.org/licenses/by-nc-nd/4.0/
Accession Number: edsbas.8B37A90
Database: BASE