PAK1 and NF2/Merlin jointly drive myelination by remodeling actin cytoskeleton in oligodendrocytes

Baudouin, L.; Ades, N.; Kante, K.; Bachelin, C.; Hmidan, H.; Deboux, C.; Panic, R.; Ben Messaoud, R.; Hamada, S.; Pionneau, C.; Velut, Y.; Duarte, K.; Poën-Guyon, S.; Barnier, J.-V.; Nait Oumesmar, B.; Bouslama-Oueghlani, L.

doi:10.1101/2023.10.16.555467

bioRxiv · 10.1101/2023.10.16.555467

PAK1 and NF2/Merlin jointly drive myelination by remodeling actin cytoskeleton in oligodendrocytes

Baudouin, L.·Ades, N.·Kante, K.·Bachelin, C.·Hmidan, H.·Deboux, C.·Panic, R.·Ben Messaoud, R.·Hamada, S.·Pionneau, C.·Velut, Y.·Duarte, K.·Poën-Guyon, S.·Barnier, J.-V.·Nait Oumesmar, B.·Bouslama-Oueghlani, L.

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Abstract

In the central nervous system (CNS), myelin formation by oligodendrocytes (OLs) relies on actin dynamics. Actin polymerization supports the ensheathment step, when the OL process contacts the axon, while a drastic shift to actin depolymerization is required to enable the following step of wrapping and expansion of myelin membranes. The molecular mechanisms triggering this switch, essential for proper myelination, have yet to be elucidated. Here, we identify P21-activated kinase 1 (PAK1) as a major regulator of actin depolymerization in OLs. We show that PAK1 accumulates in OLs in a kinase inhibited form, triggering actin disassembly and, consequently, myelin expansion. Remarkably, we identify NF2/Merlin as an endogenous inhibitor of PAK1 by proteomics analysis of its binding partners. We found that Nf2 knockdown in OLs results in PAK1 activation and impairs myelin formation, and that pharmacological inhibition of PAK1 in Nf2-knockdown OLs rescues these defects. Moreover, we demonstrate that modulating PAK1 activity in OLs controls myelin expansion and provide compelling evidence indicating that specific Pak1 loss-of-function in oligodendroglia stimulates the thickening of myelin sheaths in vivo. Overall, our data indicate that PAK1-NF2/Merlin duo plays a key role in actin cytoskeleton remodeling in OLs, required for proper myelin formation. These findings have broad mechanistic and therapeutic implications for demyelinating diseases and neurodevelopmental disorders. SignificanceRemodeling actin cytoskeleton plays a crucial role in myelin formation by oligodendrocytes (OLs). Recent studies have shown that expansion and wrapping of myelin membranes around axons depends on actin depolymerization. However, the molecular mechanisms triggering this key step in myelination are not fully elucidated. Using genetic and pharmacological tools as well as proteomics analyses, we found that PAK1 (P21 Activated Kinase 1) kinase activity is maintained inhibited by NF2/Merlin in OLs to allow actin depolymerization and, consequently, myelin membrane expansion. Pak1 loss-of-function in OLs leads to an increase in myelin thickness in the white matter of adult mice, confirming the role of PAK1 inactivation in myelin membrane expansion.

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Baudouin, L., Ades, N., Kante, K., Bachelin, C., Hmidan, H., Deboux, C., Panic, R., Ben Messaoud, R., Hamada, S., Pionneau, C., Velut, Y., Duarte, K., Poën-Guyon, S., Barnier, J.-V., Nait Oumesmar, B., Bouslama-Oueghlani, L.. 2023-10-18. PAK1 and NF2/Merlin jointly drive myelination by remodeling actin cytoskeleton in oligodendrocytes. https://doi.org/10.1101/2023.10.16.555467

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