Aims: PNS myelin is formed by Schwann cells (SCs). In this study, we applied an in vitro model to study myelin formation, using bone marrow mesenchymal stem cells and adipose-derived stem cells differentiated into SC-like cells and co-cultured with dissociated adult dorsal root ganglia neurons. Methods: Immunocytochemistry, reverse transcription-PCR and western blotting techniques were used to investigate the expression of myelin proteins at both the transcriptional and translational level. Results: Transcripts for protein zero, peripheral myelin protein 22 and myelin basic protein were detected in differentiated stem cells following co-culture with neuronal cells. Furthermore, protein zero, peripheral myelin protein 22 and myelin basic proteins were recognized in the co-cultures. These results were consistent with immunostaining of myelin proteins and with observation by electron microscopy. Conclusion: Both types of adult stems cells differentiated into SC-like cells have potential to myelinate neuronal cells during regeneration, being functionally identical to SCs of the PNS.

Bone marrow- and adipose-derived stem cells show expression of myelin mRNAs and proteins / C. Mantovani, D. Mahay, M. Kingham, G. Terenghi, S.G. Shawcross, M. Wiberg. - In: REGENERATIVE MEDICINE. - ISSN 1746-0751. - 5:3(2010 May), pp. 403-410. [10.2217/rme.10.15]

Bone marrow- and adipose-derived stem cells show expression of myelin mRNAs and proteins

C. Mantovani
Primo
;
2010

Abstract

Aims: PNS myelin is formed by Schwann cells (SCs). In this study, we applied an in vitro model to study myelin formation, using bone marrow mesenchymal stem cells and adipose-derived stem cells differentiated into SC-like cells and co-cultured with dissociated adult dorsal root ganglia neurons. Methods: Immunocytochemistry, reverse transcription-PCR and western blotting techniques were used to investigate the expression of myelin proteins at both the transcriptional and translational level. Results: Transcripts for protein zero, peripheral myelin protein 22 and myelin basic protein were detected in differentiated stem cells following co-culture with neuronal cells. Furthermore, protein zero, peripheral myelin protein 22 and myelin basic proteins were recognized in the co-cultures. These results were consistent with immunostaining of myelin proteins and with observation by electron microscopy. Conclusion: Both types of adult stems cells differentiated into SC-like cells have potential to myelinate neuronal cells during regeneration, being functionally identical to SCs of the PNS.
Gene Expression Regulation ; Adipose Tissue ; Adult ; Animals ; Animals, Newborn ; Bone Marrow Cells ; Cell Differentiation ; Humans ; Immunohistochemistry ; Microscopy, Electron, Scanning ; Myelin Sheath ; Protein Biosynthesis ; RNA, Messenger ; Rats ; Stem Cells ; Transcription, Genetic
Settore MED/13 - Endocrinologia
mag-2010
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/232533
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