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Differentiation of a Human Neural Stem Cell Line on Three Dimensional Cultures, Analysis of MicroRNA and Putative Target Genes
Published on: April 12, 2015
MicroRNA-124 regulates neuronal differentiation of mesenchymal stem cells by targeting Sp1 mRNA
Mahdieh Mondanizadeh1, Ehsan Arefian, Ghasem Mosayebi
1Research Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Abstract:
MicroRNAs play an important role in neuronal development and function. miR-124 is the most abundantly expressed miRNA in the nervous system. Several different mRNA targets have been proposed for miR-124, but the precise function of endogenous miR-124 and its mRNA targets remain to be further elucidated. Specificity protein 1 (Sp1) is a transcription factor that plays key roles in many cell processes including cell cycle. However, this transcription factor is nearly absent in differentiated neurons and a remarkable suppression of Sp1 expression was shown after neurogenesis. Since miR-124 is expressed abundantly in neurons and because Sp1 levels decrease during neurogenesis, it is possible that miR-124 could regulate the expression of Sp1 during neuronal development. Therefore, the aim of the present study was to evaluate the putative targeting of Sp1 by miR-124. Overexpression of miR-124 using a plasmid coding for pri-miR-124 in HEK293 cells decreased the expression of Sp1 mRNA. The results of dual-luciferase reporter assay demonstrated that miR-124 directly targeted the 3'-untranslated regions of Sp1 mRNA. To evaluate whether Sp1 expression was regulated by miR-124 during the process of neuronal differentiation, Adipose-derived mesenchymal stem cells (A-MSCs) were differentiated into neuron-like cells. The results of qPCR analysis showed that with the gradual increase of miR-124 expression during neurogenesis, the expression of Sp1 mRNA decreased accordingly. In summary, this study demonstrated for the first time that miR-124 is able to suppress Sp1 expression, which in turn affected the neuronal differentiation of mesenchymal stem cells.
Insights
MicroRNA-124 (miR-124) suppresses Specificity protein 1 (Sp1) expression during neuronal development. This study shows miR-124 directly targets Sp1 mRNA, impacting mesenchymal stem cell differentiation into neurons.
Area of Science:
- Neuroscience
- Molecular Biology
- Stem Cell Biology
Background:
- MicroRNAs are crucial regulators of neuronal development and function.
- miR-124 is highly expressed in the nervous system, but its precise targets and functions require further investigation.
- Specificity protein 1 (Sp1) is a transcription factor downregulated during neurogenesis, suggesting a potential regulatory relationship with miR-124.
Purpose of the Study:
- To investigate the potential targeting of Sp1 by miR-124 during neuronal development.
- To elucidate the role of miR-124 in regulating Sp1 expression in the context of neurogenesis.
Main Methods:
- Overexpression of miR-124 in HEK293 cells to assess Sp1 mRNA levels.
- Dual-luciferase reporter assays to confirm direct targeting of Sp1 mRNA's 3'-untranslated region by miR-124.
- Neuronal differentiation of Adipose-derived mesenchymal stem cells (A-MSCs) with quantitative PCR (qPCR) analysis of miR-124 and Sp1 mRNA expression.
Main Results:
- Overexpression of miR-124 led to decreased Sp1 mRNA expression in HEK293 cells.
- miR-124 was confirmed to directly target the 3'-untranslated region of Sp1 mRNA.
- During A-MSC differentiation into neuron-like cells, increasing miR-124 expression correlated with decreasing Sp1 mRNA levels.
Conclusions:
- This study provides the first evidence that miR-124 directly suppresses Sp1 expression.
- The miR-124-mediated downregulation of Sp1 influences the neuronal differentiation of mesenchymal stem cells.
- These findings highlight a novel regulatory mechanism in neuronal development involving miR-124 and Sp1.
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