PP4-dependent HDAC3 dephosphorylation discriminates between axonal regeneration and regenerative failure

Hervera, A.; Zhou, L.; Palmisano, I.; McLachlan, E.; Kong, G.; Hutson, T. H.; Danzi, M. C.; Lemmon, V. P.; Bixby, J. L.; Matamoros-Angles, A.; Forsberg, K.; De Virgiliis, F.; Matheos, D. P.; Kwapis, J.; Wood, M. A.; Puttagunta, R.; Del Rio, J. A.; Di Giovanni, S.

doi:10.1101/446963

bioRxiv · 10.1101/446963

PP4-dependent HDAC3 dephosphorylation discriminates between axonal regeneration and regenerative failure

Hervera, A.·Zhou, L.·Palmisano, I.·McLachlan, E.·Kong, G.·Hutson, T. H.·Danzi, M. C.·Lemmon, V. P.·Bixby, J. L.·Matamoros-Angles, A.·Forsberg, K.·De Virgiliis, F.·Matheos, D. P.·Kwapis, J.·Wood, M. A.·Puttagunta, R.·Del Rio, J. A.·Di Giovanni, S.

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Abstract

The molecular mechanisms discriminating between regenerative failure and success remain elusive. While a regeneration-competent peripheral nerve injury mounts a regenerative gene expression response in bipolar dorsal root ganglia (DRG) sensory neurons, a regeneration-incompetent central spinal cord injury does not. This dichotomic response offers a unique opportunity to investigate the fundamental biological mechanisms underpinning regenerative ability. Following a pharmacological screen with small molecule inhibitors targeting key epigenetic enzymes in DRG neurons we identified HDAC3 signalling as a novel candidate brake to axonal regenerative growth. In vivo, we determined that only a regenerative peripheral but not a central spinal injury induces an increase in calcium, which activates protein phosphatase 4 that in turn dephosphorylates HDAC3 thus impairing its activity and enhancing histone acetylation. Bioinformatics analysis of ex vivo H3K9ac ChIPseq and RNAseq from DRG followed by promoter acetylation and protein expression studies implicated HDAC3 in the regulation of multiple regenerative pathways. Finally, genetic or pharmacological HDAC3 inhibition overcame regenerative failure of sensory axons following spinal cord injury. Together, these data indicate that PP4-dependent HDAC3 dephosphorylation discriminates between axonal regeneration and regenerative failure.\n\n\n\nO_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=122 SRC=\"FIGDIR/small/446963_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (40K):\norg.highwire.dtl.DTLVardef@1bd577corg.highwire.dtl.DTLVardef@1ba990aorg.highwire.dtl.DTLVardef@195813corg.highwire.dtl.DTLVardef@57abc7_HPS_FORMAT_FIGEXP M_FIG Graphical AbstractFollowing central nervous system (CNS) spinal injury, protein phosphatase 4/2 activity is not induced since calcium levels remain unchanged compared to uninjured conditions. HDAC3 remains phosphorylated and occupies deacetylated chromatin contributing to its compaction inhibiting gene expression. Following peripheral nervous system (PNS) sciatic injury, protein phosphatase 4/2 activity is induced by calcium. HDAC3 is dephosphorylated leading to its inhibition and release from chromatin sites contributing to increase in histone acetylation and in the expression of regeneration associated genes (RAGs).\n\nC_FIG

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Hervera, A., Zhou, L., Palmisano, I., McLachlan, E., Kong, G., Hutson, T. H., Danzi, M. C., Lemmon, V. P., Bixby, J. L., Matamoros-Angles, A., Forsberg, K., De Virgiliis, F., Matheos, D. P., Kwapis, J., Wood, M. A., Puttagunta, R., Del Rio, J. A., Di Giovanni, S.. 2018-10-18. PP4-dependent HDAC3 dephosphorylation discriminates between axonal regeneration and regenerative failure. https://doi.org/10.1101/446963

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