TDP-43 Proteinopathy and ALS: Insights into Disease Mechanisms and Therapeutic Targets

• Published in: Neurotherapeutics 2015-04, Vol.12 (2), p.352-363
• Main Authors: Scotter, Emma L., Chen, Han-Jou, Shaw, Christopher E.
• Format: Article
• Language: English
• Subjects: Amyotrophic lateral sclerosis; Amyotrophic Lateral Sclerosis - genetics; Amyotrophic Lateral Sclerosis - metabolism; Amyotrophic Lateral Sclerosis - therapy; Animals; Biomedical and Life Sciences; Biomedicine; Dementia; Disease; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Environment; Gene Silencing - physiology; Health risk assessment; Humans; Mutation; Mutation - genetics; Neurobiology; Neurology; Neurons; Neurosciences; Neurosurgery; Pathogenesis; Proteins; Review; TDP-43 Proteinopathies - genetics; TDP-43 Proteinopathies - metabolism; TDP-43 Proteinopathies - therapy
• ISSN: 1933-7213; 1878-7479; 1878-7479
• DOI: 10.1007/s13311-015-0338-x

Therapeutic options for patients with amyotrophic lateral sclerosis (ALS) are currently limited. However, recent studies show that almost all cases of ALS, as well as tau-negative frontotemporal dementia (FTD), share a common neuropathology characterized by the deposition of TAR-DNA binding protein (TDP)-43-positive protein inclusions, offering an attractive target for the design and testing of novel therapeutics. Here we demonstrate how diverse environmental stressors linked to stress granule formation, as well as mutations in genes encoding RNA processing proteins and protein degradation adaptors, initiate ALS pathogenesis via TDP-43. We review the progressive development of TDP-43 proteinopathy from cytoplasmic mislocalization and misfolding through to macroaggregation and the addition of phosphate and ubiquitin moieties. Drawing from cellular and animal studies, we explore the feasibility of therapeutics that act at each point in pathogenesis, from mitigating genetic risk using antisense oligonucleotides to modulating TDP-43 proteinopathy itself using small molecule activators of autophagy, the ubiquitin-proteasome system, or the chaperone network. We present the case that preventing the misfolding of TDP-43 and/or enhancing its clearance represents the most important target for effectively treating ALS and frontotemporal dementia.