Cultures of Schwann-like cells differentiated from adipose-derived stem cells on PDMS/MWNT sheets as a scaffold for peripheral nerve regeneration

Carbon nanotubes (CNTs) are promising candidates as novel scaffolds for peripheral nerve regeneration. Schwann cells (SCs) are attractive therapeutic targets due to their pivotal role in peripheral nerve regeneration, but primary SCs have limitations for clinical application. However, adipose‐derive...

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Veröffentlicht in:Journal of biomedical materials research. Part A 2015-11, Vol.103 (11), p.3642-3648
Hauptverfasser: Han, In Ho, Sun, Fangfang, Choi, Yoon Ji, Zou, Fengming, Nam, Kyoung Hyup, Cho, Won Ho, Choi, Byung Kwan, Song, Geun Sung, Koh, Kwangnak, Lee, Jaebeom
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Sprache:eng
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Zusammenfassung:Carbon nanotubes (CNTs) are promising candidates as novel scaffolds for peripheral nerve regeneration. Schwann cells (SCs) are attractive therapeutic targets due to their pivotal role in peripheral nerve regeneration, but primary SCs have limitations for clinical application. However, adipose‐derived stem cells (ASCs) may differentiate into Schwann‐like cells. The present study assesses the potential applicability of multiwall CNTs (MWNTs) composited with polydimethylsiloxane (PDMS), which were then seeded with differentiated adipose‐derived stem cells (dASCs) to promote neuronal differentiation and growth. Aqueous MWNT dispersion was filtered, and the PDMS/MWNT sheets were prepared using a simple printing‐transfer method. Characterization of PDMS/MWNT sheets indicated their unique physical properties, such as superior mechanical strength and electroconductivity, compared with bare PDMS sheets. ASCs were differentiated into Schwann‐like cells using a mixture of glial growth factors. Dorsal root ganglion (DRG) neurons were co‐cultured with SCs and dASCs on PDMS/MWNTs sheets or noncoated dishes. An alamar blue proliferation assay of dASC and SCs showed significantly more dASC and SCs cultured on PDMS/MWNT sheets at 48 h and 72 h than when cultured on noncoated dishes (p 
ISSN:1549-3296
1552-4965
DOI:10.1002/jbm.a.35488