Melatonin Enhances Neural Differentiation of Adipose-Derived Mesenchymal Stem Cells

Author:

Romano Ivana Roberta1,D’Angeli Floriana2ORCID,Gili Elisa3,Fruciano Mary3,Lombardo Giuseppe Angelo Giovanni45ORCID,Mannino Giuliana6ORCID,Vicario Nunzio1ORCID,Russo Cristina1,Parenti Rosalba1ORCID,Vancheri Carlo3ORCID,Giuffrida Rosario1ORCID,Pellitteri Rosalia7,Lo Furno Debora1ORCID

Affiliation:

1. Department of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy

2. Department of Human Sciences and Quality of Life Promotion, San Raffaele Roma Open University, 00166 Rome, Italy

3. Department of Clinical and Experimental Medicine, University of Catania, 95124 Catania, Italy

4. Faculty of Medicine and Surgery, University of Enna “Kore”, 94100 Enna, Italy

5. Cannizzaro Hospital, 95126 Catania, Italy

6. Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, 98122 Messina, Italy

7. Institute for Biomedical Research and Innovation, National Research Council, 95126 Catania, Italy

Abstract

Adipose-derived mesenchymal stem cells (ASCs) are adult multipotent stem cells, able to differentiate toward neural elements other than cells of mesodermal lineage. The aim of this research was to test ASC neural differentiation using melatonin combined with conditioned media (CM) from glial cells. Isolated from the lipoaspirate of healthy donors, ASCs were expanded in a basal growth medium before undergoing neural differentiation procedures. For this purpose, CM obtained from olfactory ensheathing cells and from Schwann cells were used. In some samples, 1 µM of melatonin was added. After 1 and 7 days of culture, cells were studied using immunocytochemistry and flow cytometry to evaluate neural marker expression (Nestin, MAP2, Synapsin I, GFAP) under different conditions. The results confirmed that a successful neural differentiation was achieved by glial CM, whereas the addition of melatonin alone did not induce appreciable changes. When melatonin was combined with CM, ASC neural differentiation was enhanced, as demonstrated by a further improvement of neuronal marker expression, whereas glial differentiation was attenuated. A dynamic modulation was also observed, testing the expression of melatonin receptors. In conclusion, our data suggest that melatonin’s neurogenic differentiation ability can be usefully exploited to obtain neuronal-like differentiated ASCs for potential therapeutic strategies.

Funder

University of Catania, Italy

Publisher

MDPI AG

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