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CDNF rescues motor neurons in three animal models of ALS by targeting ER stress

De Lorenzo, F.; Luningschror, P.; Nam, J.; Pilotto, F.; Galli, E.; Lindholm, P.; Rudt von Collenberg, C.; Tii Mungwa, S.; Kauder, J.; Jablonka, S.; Petri, S.; Lindholm, D.; Saxena, S.; Sendtner, M.; Saarma, M.; Voutilainen, M. H.

2020-09-16 neuroscience
10.1101/2020.05.05.078618 bioRxiv
Show abstract

The role of chronic endoplasmic reticulum (ER) stress in the pathophysiology of Amyotrophic lateral sclerosis (ALS), as well as a potential drug target, has received increasing attention. Here, we investigated the mode of action and therapeutic effect of the ER resident protein cerebral dopamine neurotrophic factor (CDNF) in preclinical models of ALS harboring different genetic mutations. We identify that intracerebroventricular (i.c.v.) administration of CDNF significantly halts the progression of the disease and improves motor behavior in TDP43-M337V and SOD1-G93A rodent models of ALS. CDNF rescues motor neurons (MNs) in vitro and in vivo from ER stress associated cell death and its beneficial effect is independent of genetic disease etiology. Notably, CDNF regulates the unfolded protein response (UPR) initiated by transducers IRE1, PERK, and ATF6, thereby enhancing MN survival. Thus, CDNF holds great promise for the design of new rational treatments for ALS.

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