MiR-138 promotes the migration of cultured chicken embryonic hypothalamic cells by targeting reelin
| Autor: | N. Meiri, T. Kisliouk |
|---|---|
| Rok vydání: | 2013 |
| Předmět: |
Cell Adhesion Molecules
Neuronal Cell Hypothalamus Nerve Tissue Proteins Chick Embryo Cell Movement medicine Animals Reelin 3' Untranslated Regions Cells Cultured Cell Proliferation Neurons Extracellular Matrix Proteins biology Cell growth General Neuroscience Serine Endopeptidases Cell migration Embryonic stem cell Neural stem cell Cell biology MicroRNAs Reelin Protein medicine.anatomical_structure Cell culture biology.protein Ectopic expression Neuroscience Signal Transduction |
| Zdroj: | Neuroscience. 238:114-124 |
| ISSN: | 0306-4522 |
| DOI: | 10.1016/j.neuroscience.2013.02.020 |
| Popis: | Neuronal network remodeling during critical periods of sensory development might be accompanied by alterations in hypothalamic cell populations. MicroRNAs play a central role in regulating neuronal function, including neural stem cell proliferation, and neuronal migration, maturation and integration into viable circuits by modulating different mRNA targets. Here we investigated the role of miR-138 in cell proliferation and migration in a neuron-enriched hypothalamic cell culture prepared from chicks on embryonic day 16. Ectopic expression of miR-138 enhanced hypothalamic cell migration, but did not affect cell proliferation. As a potential mechanism for miR-138’s effect on cell migration, we investigated reelin (Reln) as a direct target of miR-138. Luciferase reporter assay and Ago2-immunoprecipitation experiments confirmed direct binding of miR-138 to the Reln 3′-untranslated region. Ectopic miR-138 abolished Reln levels in hypothalamic cells and enhanced their migration, similar to Reln-antisense DNA. Furthermore, inhibition of Reln expression by miR-138 led to decreased phosphorylation level of the key component of Reln-regulated signaling cascades, Disabled 1. These findings describe miR-138 as a novel regulator of hypothalamic cell migration, acting at least in part via inhibition of Reln expression and leading to the inactivation of Reln signals. |
| Databáze: | OpenAIRE |
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