Effects of TDP-43 overexpression on neuron proteome and morphology in vitro

• Published in: Molecular and cellular neuroscience 2021-07, Vol.114, p.103627-103627, Article 103627
• Main Authors: Atkinson, Rachel A.K., Fair, Hannah L., Wilson, Richard, Vickers, James C., King, Anna E.
• Format: Article
• Language: English
• Subjects: ALS; Amyotrophic Lateral Sclerosis - genetics; Amyotrophic Lateral Sclerosis - metabolism; Animals; Cell Shape - physiology; Cerebral Cortex - metabolism; Cytoskeleton - genetics; Cytoskeleton - metabolism; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Frontotemporal Lobar Degeneration - genetics; Frontotemporal Lobar Degeneration - metabolism; FTLD; Mice; Mice, Transgenic; Neurites - metabolism; Neuron morphology; Neuronal Outgrowth - genetics; Neurons - metabolism; Proteome - genetics; Proteome - metabolism; Proteomics; TDP-43
• ISSN: 1044-7431; 1095-9327
• DOI: 10.1016/j.mcn.2021.103627

TDP-43 is pathologically and genetically with associated amyotrophic lateral sclerosis and frontotemporal lobar degeneration. These diseases are characterized by significant neurite defects, including cytoskeletal pathology. The involvement of TDP-43 in the degeneration of neurons in these diseases are not yet well understood, however accumulating evidence shows involvement in neurite outgrowth, remodelling and in regulation of many components of the neuronal cytoskeleton. In order to investigate how alterations to TDP-43 expression levels may exert effects on the neuronal cytoskeleton, primary cortical neurons from transgenic mice overexpressing one or two copies of human wildtype TDP-43 under the prion promoter were examined. Label-free quantitative proteomic analysis, followed by functional annotation clustering to identify protein families that clustered together within up- or down-regulated protein groups, revealed that actin-binding proteins were significantly more abundant in neurons overexpressing TDP-43 compared to wildtype neurons. Morphological analysis demonstrated that during early development neurons expressing one copy of human TDP-43 had an increased number of neurite branches and alterations to growth cone morphology, while no changes were observed in neurons expressing two copies of TDP-43. These developmental processes require specific expression and organization of the cytoskeleton. The results from these studies provide further insight into the normal function of TDP-43 and how alterations in TDP-43 expression may impact the cytoskeleton. •TDP-43 overexpression in cultured neurons resulted in alterations to neurite branching and growth cone morphology•Proteomic analysis of neurons overexpressing TDP-43 revealed actin-binding proteins were significantly altered•Provides insight into the relationship between TDP-43 and the neuronal cytoskeleton