Disruption of ER‐mitochondria tethering and signalling in C9orf72‐associated amyotrophic lateral sclerosis and frontotemporal dementia. Issue 2 (13th January 2022)

• Record Type: Journal Article
• Authors: Gomez‐Suaga, Patricia; Mórotz, Gábor M.; Markovinovic, Andrea; Martín‐Guerrero, Sandra M.; Preza, Elisavet; Arias, Natalia; Mayl, Keith; Aabdien, Afra; Gesheva, Vesela; Nishimura, Agnes; Annibali, Ambra; Lee, Younbok; Mitchell, Jacqueline C.; Wray, Selina; Shaw, Christopher; Noble, Wendy; Miller, Christopher C. J.
• Is Part Of: Aging cell. Volume 21:Issue 2(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-01-13
• Subjects: amyotrophic lateral sclerosis -- C9orf72 -- endoplasmic reticulum -- frontotemporal dementia -- GSK3β -- mitochondria -- PTPIP51 -- VAPB; Cells -- Aging -- Periodicals; 571.8783605
• DOI: 10.1111/acel.13549
• Languages: English
• ISSNs: 1474-9718

Abstract

Abstract: Hexanucleotide repeat expansions in C9orf72 are the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). The mechanisms by which the expansions cause disease are not properly understood but a favoured route involves its translation into dipeptide repeat (DPR) polypeptides, some of which are neurotoxic. However, the precise targets for mutant C9orf72 and DPR toxicity are not fully clear, and damage to several neuronal functions has been described. Many of these functions are regulated by signalling between the endoplasmic reticulum (ER) and mitochondria. ER‐mitochondria signalling requires close physical contacts between the two organelles that are mediated by the VAPB‐PTPIP51 'tethering' proteins. Here, we show that ER‐mitochondria signalling and the VAPB‐PTPIP51 tethers are disrupted in neurons derived from induced pluripotent stem (iPS) cells from patients carrying ALS/FTD pathogenic C9orf72 expansions and in affected neurons in mutant C9orf72 transgenic mice. In these mice, disruption of the VAPB‐PTPIP51 tethers occurs prior to disease onset suggesting that it contributes to the pathogenic process. We also show that neurotoxic DPRs disrupt the VAPB‐PTPIP51 interaction and ER‐mitochondria contacts and that this may involve activation of glycogen synthase kinases‐3β (GSK3β), a known negative regulator of VAPB‐PTPIP51 binding. Finally, we show that these DPRs disrupt delivery of Ca 2+ from ER stores to mitochondria, which is a primary function of the VAPB‐PTPIP51 tethers. This delivery regulates a number of key neuronal functions that are damaged in ALS/FTD including bioenergetics, autophagy and synaptic function. Our findings reveal a new molecular target for mutant C9orf72 ‐mediated toxicity. Abstract : Model depicting mechanisms linking ALS/FTD‐mutant C9orf72 with disruption of the VAPB‐PTPIP51 interaction, synaptic activity and neurodegeneration. C9orf72 ‐derived toxic DPRs activate GSK3β leading to breaking of the VAPB‐PTPIP51 tethers. This perturbs IP3 receptor‐mediated delivery of Ca 2+ from ER to mitochondria to damage synaptic function and induce neurodegeneration. ALS/FTD linked TDP‐43 and FUS also disrupt the VAPB‐PTPIP51 interaction via activation of GSK3β ( Nature Communications, 5, 3996; EMBO Reports, 17, 1326).