Graphene Oxide Substrate Promotes Neurotrophic Factor Secretion and Survival of Human Schwann-Like Adipose Mesenchymal Stromal Cells.

Schwann cells adipose stem cells graphene oxide nerve regeneration peripheral nerve injuries

Journal

Advanced biology
ISSN: 2701-0198
Titre abrégé: Adv Biol (Weinh)
Pays: Germany
ID NLM: 101775319

Informations de publication

Date de publication:
04 2021
Historique:
revised: 04 02 2021
received: 10 09 2020
entrez: 14 4 2021
pubmed: 15 4 2021
medline: 26 10 2021
Statut: ppublish

Résumé

Mesenchymal stromal cells from adipose tissue (AD-MSCs) exhibit favorable clinical traits for autologous transplantation and can develop 'Schwann-like' phenotypes (sAD-MSCs) to improve peripheral nerve regeneration, where severe injuries yield insufficient recovery. However, sAD-MSCs regress without biochemical stimulation and detach from conduits under unfavorable transplant conditions, negating their paracrine effects. Graphene-derived materials support AD-MSC attachment, regulating cell adhesion and function through physiochemistry and topography. Graphene oxide (GO) is a suitable substrate for human sAD-MSCs incubation toward severe peripheral nerve injuries by evaluating transcriptome changes, neurotrophic factor expression over a 7-days period, and cell viability in apoptotic conditions is reported. Transcriptome changes from GO incubation across four patients are minor compared to biological variance. Nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and glial-derived neurotrophic factor (GDNF) gene expression is unchanged from sAD-MSCs on GO substrates, but NGF and GDNF protein secretion increase at day 3 and 7. Secretome changes do not improve dorsal root ganglia neuron axon regeneration in conditioned media culture models. Fewer sAD-MSCs detach from GO substrates compared to glass following phosphate buffer saline exposure, which simulates apoptotic conditions. Overall, GO substrates are compatible with sAD-MSC primed for peripheral nerve regeneration strategies and protect the cell population in harsh environments.

Identifiants

pubmed: 33852181
doi: 10.1002/adbi.202000271
doi:

Substances chimiques

graphene oxide 0
Graphite 7782-42-5

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2000271

Informations de copyright

© 2021 The Authors. Advanced Biology published by Wiley-VCH GmbH.

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Auteurs

Steffan H Llewellyn (SH)

Blond McIndoe Laboratories, Division of Cell Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PL, UK.
Department of Materials and National Graphene Institute, The University of Manchester, Manchester, M13 9PL, UK.

Alessandro Faroni (A)

Blond McIndoe Laboratories, Division of Cell Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PL, UK.

Maria Iliut (M)

Department of Materials and National Graphene Institute, The University of Manchester, Manchester, M13 9PL, UK.

Cian Bartlam (C)

Department of Materials and National Graphene Institute, The University of Manchester, Manchester, M13 9PL, UK.
Institute of Physics, EIT 2, Bundeswehr University Munich, Neubiberg, 85577, Germany.

Aravind Vijayaraghavan (A)

Department of Materials and National Graphene Institute, The University of Manchester, Manchester, M13 9PL, UK.

Adam J Reid (AJ)

Blond McIndoe Laboratories, Division of Cell Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PL, UK.
Department of Plastic Surgery & Burns, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, M23 9LT, UK.

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