Development and in vitro differentiation of Schwann cells

• Verfasst von: Hörner, Sarah J. [VerfasserIn]
• Verfasst von: Couturier, Nathalie [VerfasserIn]
• Verfasst von: Gueiber, Daniele Caroline [VerfasserIn]
• Verfasst von: Hafner, Mathias [VerfasserIn]
• Verfasst von: Rudolf, Rüdiger [VerfasserIn]
• Titel: Development and in vitro differentiation of Schwann cells
• Verf.angabe: Sarah Janice Hörner, Nathalie Couturier, Daniele Caroline Gueiber, Mathias Hafner and Rüdiger Rudolf
• E-Jahr: 2022
• Jahr: 24 November 2022
• Umfang: 43 S.
• Illustrationen: Illustrationen
• Fussnoten: Gesehen am 02.09.2024
• Titel Quelle: Enthalten in: Cells
• Ort Quelle: Basel : MDPI, 2012
• Jahr Quelle: 2022
• Band/Heft Quelle: 11(2022), 23, Artikel-ID 3753, Seite 1-43
• ISSN Quelle: 2073-4409
• DOI: doi:10.3390/cells11233753
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: differentiation
• Sach-SW: glia
• Sach-SW: hiPSC
• Sach-SW: MSC
• Sach-SW: neural crest
• Sach-SW: Schwann cells
• Sach-SW: stem cells
• Sach-SW: tissue engineering
• K10plus-PPN: 1900840472

Abstract

Schwann cells are glial cells of the peripheral nervous system. They exist in several subtypes and perform a variety of functions in nerves. Their derivation and culture in vitro are interesting for applications ranging from disease modeling to tissue engineering. Since primary human Schwann cells are challenging to obtain in large quantities, in vitro differentiation from other cell types presents an alternative. Here, we first review the current knowledge on the developmental signaling mechanisms that determine neural crest and Schwann cell differentiation in vivo. Next, an overview of studies on the in vitro differentiation of Schwann cells from multipotent stem cell sources is provided. The molecules frequently used in those protocols and their involvement in the relevant signaling pathways are put into context and discussed. Focusing on hiPSC- and hESC-based studies, different protocols are described and compared, regarding cell sources, differentiation methods, characterization of cells, and protocol efficiency. A brief insight into developments regarding the culture and differentiation of Schwann cells in 3D is given. In summary, this contribution provides an overview of the current resources and methods for the differentiation of Schwann cells, it supports the comparison and refinement of protocols and aids the choice of suitable methods for specific applications.