Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8840766 | Neuroscience | 2018 | 28 Pages |
Abstract
Following peripheral nerve injury, Schwann Cells (SCs) undergo dedifferentiation, proliferation, migration, and remyelination. Recent works demonstrated the importance of the short non-coding RNA (miRNAs) in SC dedifferentiation and remyelination after nerve injury. Previously, we found some miRNAs like miR-9, miR-221, miR-222 and miR-182 could regulate the proliferation and migration of SCs. Therefore, it is imperative to ask whether these miRNAs could regulate the myelination of SCs. Here we demonstrated that miR-221-3p could inhibit the myelination of SCs when co-cultured with dorsal root ganglion cells in vitro. In addition, NGF1-A binding protein 1 (Nab1) which was essential for SCs myelination could be downregulated by miR-221-3p. Suppressing the expression of Nab1 could reverse the promotion of miR-221-3p antagomir on SC myelination. The effects of miR-221-3p on SC myelination might be used to improve peripheral nerve regeneration, thus offering a new approach to peripheral nerve repair.
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Neuroscience
Neuroscience (General)
Authors
Lili Zhao, Ying Yuan, Ping Li, Jiacheng Pan, Jing Qin, Yisheng Liu, Yu Zhang, Feng Tian, Bin Yu, Songlin Zhou,