Activation of XBP1s attenuates disease severity in models of proteotoxic Charcot–Marie–Tooth type 1B

• Published in: Brain (London, England : 1878) Vol. 148; no. 6; pp. 1978 - 1993
• Main Authors: Touvier, Thierry, Veneri, Francesca A, Claessens, Anke, Ferri, Cinzia, Mastrangelo, Rosa, Sorgiati, Noémie, Bianchi, Francesca, Valenzano, Serena, Del Carro, Ubaldo, Rivellini, Cristina, Duong, Phu, Shy, Michael E, Kelly, Jeffery W, Svaren, John, Wiseman, R Luke, D’Antonio, Maurizio
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 03.06.2025
• Subjects: Animals; Charcot-Marie-Tooth Disease - genetics; Charcot-Marie-Tooth Disease - metabolism; Charcot-Marie-Tooth Disease - pathology; Disease Models, Animal; Endoplasmic Reticulum Stress - physiology; Endoribonucleases - metabolism; Mice; Mice, Inbred C57BL; Mice, Transgenic; Myelin P0 Protein - genetics; Myelin P0 Protein - metabolism; Myelin Sheath - metabolism; Original; Protein Serine-Threonine Kinases - metabolism; Schwann Cells - metabolism; Unfolded Protein Response; X-Box Binding Protein 1 - genetics; X-Box Binding Protein 1 - metabolism; unfolded protein response; Charcot–Marie–Tooth; XBP1; proteostasis; Schwann cell; demyelinating neuropathy
• ISSN: 0006-8950; 1460-2156; 1460-2156
• DOI: 10.1093/brain/awae407

Mutations in myelin protein zero (MPZ) are generally associated with Charcot–Marie–Tooth type 1B (CMT1B) disease, one of the most common forms of demyelinating neuropathy. Pathogenesis of some MPZ mutants, such as S63del and R98C, involves the misfolding and retention of MPZ in the endoplasmic reticulum (ER) of myelinating Schwann cells. To cope with proteotoxic ER stress, Schwann cells mount an unfolded protein response (UPR) characterized by activation of the PERK, ATF6 and IRE1α/XBP1 pathways. Previous results showed that targeting the PERK UPR pathway mitigates neuropathy in mouse models of CMT1B; however, the contributions of other UPR pathways in disease pathogenesis remain poorly understood. Here, we probe the importance of IRE1α/XBP1 signalling during normal myelination and in CMT1B. In response to ER stress, IRE1α is activated to stimulate the non-canonical splicing of Xbp1 mRNA to generate spliced Xbp1 (Xbp1s). This results in the increased expression of the adaptive transcription factor XBP1s, which regulates the expression of genes involved in diverse pathways, including ER proteostasis. We generated mouse models in which Xbp1 is deleted specifically in Schwann cells, preventing XBP1s activation in these cells. We observed that Xbp1 is dispensable for normal developmental myelination, myelin maintenance and remyelination after injury. However, Xbp1 deletion dramatically worsens the hypomyelination and the electrophysiological and locomotor parameters observed in young and adult CMT1B neuropathic animals. RNA-sequencing analysis suggested that XBP1s exerts its adaptive function in CMT1B mouse models in large part via the induction of ER proteostasis genes. Accordingly, the exacerbation of the neuropathy in Xbp1-deficient mice was accompanied by upregulation of ER-stress pathways and of regulated IRE1α-dependent mRNA decay signalling in Schwann cells, suggesting that the activation of XBP1s via IRE1α plays a crucial role in limiting mutant protein toxicity and that this toxicity cannot be compensated by other stress responses. Schwann cell-specific overexpression of XBP1s partly re-established Schwann cell proteostasis and attenuated CMT1B severity in both the S63del and R98C mouse models. In addition, the selective, pharmacological activation of IRE1α/XBP1 signalling ameliorated myelination in S63del dorsal root ganglia explants. Collectively, these data show that XBP1 has an essential adaptive role in different models of proteotoxic CMT1B neuropathy and suggest that activation of the IRE1α/XBP1 pathway might represent a therapeutic avenue in CMT1B and, possibly, for other neuropathies characterized by UPR activation.