Roles of miR-432 and circ_0000418 in mediating the anti-depressant action of ADAR1
Adenosine deaminase acting on RNA1 (ADAR1) is a newly discovered epigenetic molecule marker that is sensitive to environmental stressors. A recent study has demonstrated that ADAR1 affects BDNF expression via miR-432 and is involved in antidepressant action. However, the detailed molecular mechanism...
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Veröffentlicht in: | Neurobiology of stress 2021-11, Vol.15, p.100396-100396, Article 100396 |
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Sprache: | eng |
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Zusammenfassung: | Adenosine deaminase acting on RNA1 (ADAR1) is a newly discovered epigenetic molecule marker that is sensitive to environmental stressors. A recent study has demonstrated that ADAR1 affects BDNF expression via miR-432 and is involved in antidepressant action. However, the detailed molecular mechanism is still unclear. We have uncovered a new molecular mechanism showing the involvement of miR-432 and circ_0000418 in mediating the antidepressant action of ADAR1. We demonstrate that the ADAR1 inducer (IFN-γ) alleviates the depressive-like behaviors of BALB/c mice treated with chronic unpredictable stress (CUS) exposure. Moreover, both in vivo and in vitro studies show that ADAR1 differently impacts miR-432 and circ_0000418 expressions. Furthermore, the in vitro results demonstrate that circ_0000418 oppositely affects BDNF expression. Together, our results indicate that ADAR1 affects CUS-induced depressive-like behavior and BDNF expression by acting on miR-432 and circ_0000418. Elucidation of this new molecular mechanism will not only provide insights into further understanding the important role of ADAR1 in stress-induced depressive-like behavior but also suggest a potential therapeutic strategy for developing novel anti-depressive drugs.
•MiR-432 and circ_0000418 mediates the antidepressant action of ADAR1.•MiR-432 and circ_0000418 interactively affect BDNF expression.•LIN28B is involved in the interaction among ADAR1, miR-432, and circ_0000418.•HNRNPC is involved in the regulatory role of circ_0000418 on BDNF. |
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ISSN: | 2352-2895 2352-2895 |
DOI: | 10.1016/j.ynstr.2021.100396 |