Melatonin Enhances Neural Differentiation of Adipose-Derived Mesenchymal Stem Cells.
Ivana Roberta RomanoFloriana D'AngeliElisa GiliMary FrucianoGiuseppe Angelo Giovanni LombardoGiuliana ManninoNunzio VicarioCristina RussoRosalba ParentiCarlo VancheriRosario GiuffridaRosalia PellitteriDebora Lo FurnoPublished in: International journal of molecular sciences (2024)
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.
Keyphrases
- induced apoptosis
- mesenchymal stem cells
- cell cycle arrest
- stem cells
- poor prognosis
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- flow cytometry
- bone marrow
- umbilical cord
- neuropathic pain
- risk assessment
- single cell
- climate change
- cell therapy
- blood brain barrier
- binding protein
- long non coding rna
- artificial intelligence
- data analysis
- peripheral nerve