Abstract
Background: The AKT/mTOR/p70S6K pathway has been shown to potentially promote spinal cord injury (SCI) repair in rats. However, its exact mechanism and beyond needs to be further explored.
Objective: This study aims to explore the AKT/mTOR/p70S6K pathway in oligodendrocyte precursor cell (OPC) differentiation, microglial polarization differentiation, and the role of these in myelin regeneration in vitro.
Methods: The isolation, induction and characterization of rat primary neuronal stem cells, OPCs and oligodendrocytes were investigated with immunofluorescence and RT-qPCR. Then, the role of AKT/mTOR/p70S6K signaling was explored using western blotting and immunofluorescence, the effect on myelination was examined with OPC-dorsal root ganglion (DRG) neurons co-culture, and the influence of M1/M2 polarization status of microglia on myelin formation was also observed by adding M1/M2 supernatants into OPC-DRG neurons co-culture.
Results: Activation of the AKT/mTOR/p70S6K pathway elevated the expression of oligodendrocyte differentiation markers, including MBP, PLP and MOG, which also promoted the colocalization of MBP and NFH in OPC-DRG neurons co-culture. More interestingly, stimulation of the AKT/mTOR/p70S6K pathway facilitated M2 polarization of rat microglia. M2 polarization of microglia enhanced OPC differentiation to oligodendrocytes and myelin formation.
Conclusion: Our findings highlight the potential of targeting the AKT/mTOR/p70S6K pathway in promoting oligodendrocyte differentiation and myelin regeneration in neurological disorders such as SCI.
[http://dx.doi.org/10.1016/j.ceb.2021.05.003] [PMID: 34153742]
[http://dx.doi.org/10.2174/1381612822666151204000636] [PMID: 26635271]
[http://dx.doi.org/10.3390/cells8111424] [PMID: 31726662]
[http://dx.doi.org/10.3390/cells8101236] [PMID: 31614602]
[http://dx.doi.org/10.1007/s13311-011-0033-5] [PMID: 21404073]
[http://dx.doi.org/10.1093/brain/awac406] [PMID: 36325693]
[http://dx.doi.org/10.1016/j.expneurol.2016.03.008]
[http://dx.doi.org/10.18632/oncotarget.23538] [PMID: 29560097]
[http://dx.doi.org/10.1016/j.ejmech.2020.112820] [PMID: 32966896]
[http://dx.doi.org/10.1080/02688697.2020.1862056] [PMID: 33345640]
[http://dx.doi.org/10.1155/2017/5150678] [PMID: 29410971]
[http://dx.doi.org/10.1016/j.ejphar.2020.173090] [PMID: 32234529]
[http://dx.doi.org/10.3389/fnagi.2022.815347] [PMID: 35250543]
[http://dx.doi.org/10.7150/thno.68895] [PMID: 35547763]
[http://dx.doi.org/10.5607/en.2017.26.1.33] [PMID: 28243165]
[http://dx.doi.org/10.1186/s12974-016-0660-1] [PMID: 27549161]
[http://dx.doi.org/10.1016/j.expneurol.2020.113372] [PMID: 32504636]
[http://dx.doi.org/10.1038/nrn2495] [PMID: 19096367]
[http://dx.doi.org/10.1371/journal.pone.0047645] [PMID: 23091637]
[http://dx.doi.org/10.1016/j.cell.2012.12.006] [PMID: 23332759]
[http://dx.doi.org/10.1093/brain/awn334] [PMID: 19208690]
[http://dx.doi.org/10.1002/glia.22281] [PMID: 22144101]
[http://dx.doi.org/10.1038/s41467-022-31797-0] [PMID: 35835751]
[http://dx.doi.org/10.1523/JNEUROSCI.3257-09.2009] [PMID: 19864556]
[http://dx.doi.org/10.1523/JNEUROSCI.1661-07.2007] [PMID: 17634369]
[http://dx.doi.org/10.1523/JNEUROSCI.22-10-03921.2002] [PMID: 12019311]
[http://dx.doi.org/10.1038/nn.3469] [PMID: 23872599]
[http://dx.doi.org/10.1523/JNEUROSCI.1619-13.2014] [PMID: 24501362]
[http://dx.doi.org/10.1007/s12031-008-9053-y]
[http://dx.doi.org/10.1189/jlb.0406249] [PMID: 16905575]
[http://dx.doi.org/10.1002/glia.21266] [PMID: 22072381]
[http://dx.doi.org/10.1002/brb3.152] [PMID: 24392271]