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| Home > Publications Database > Mis-localization of endogenous TDP-43 leads to ALS-like early-stage metabolic dysfunction and progressive motor deficits. > print |
| Home > Publications Database > Mis-localization of endogenous TDP-43 leads to ALS-like early-stage metabolic dysfunction and progressive motor deficits. > print |
| 001 | 270416 | ||
| 005 | 20240809090118.0 | ||
| 024 | 7 | _ | |a pmc:PMC11188230 |2 pmc |
| 024 | 7 | _ | |a 10.1186/s13024-024-00735-7 |2 doi |
| 024 | 7 | _ | |a pmid:38902734 |2 pmid |
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| 037 | _ | _ | |a DZNE-2024-00796 |
| 041 | _ | _ | |a English |
| 082 | _ | _ | |a 570 |
| 100 | 1 | _ | |a Hu, Yiying |0 P:(DE-2719)9000587 |b 0 |e First author |u dzne |
| 245 | _ | _ | |a Mis-localization of endogenous TDP-43 leads to ALS-like early-stage metabolic dysfunction and progressive motor deficits. |
| 260 | _ | _ | |a London |c 2024 |b Biomed Central |
| 336 | 7 | _ | |a article |2 DRIVER |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1718977151_18080 |2 PUB:(DE-HGF) |
| 336 | 7 | _ | |a ARTICLE |2 BibTeX |
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| 336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
| 520 | _ | _ | |a The key pathological signature of ALS/ FTLD is the mis-localization of endogenous TDP-43 from the nucleus to the cytoplasm. However, TDP-43 gain of function in the cytoplasm is still poorly understood since TDP-43 animal models recapitulating mis-localization of endogenous TDP-43 from the nucleus to the cytoplasm are missing.CRISPR/Cas9 technology was used to generate a zebrafish line (called CytoTDP), that mis-locates endogenous TDP-43 from the nucleus to the cytoplasm. Phenotypic characterization of motor neurons and the neuromuscular junction was performed by immunostaining, microglia were immunohistochemically localized by whole-mount tissue clearing and muscle ultrastructure was analyzed by scanning electron microscopy. Behavior was investigated by video tracking and quantitative analysis of swimming parameters. RNA sequencing was used to identify mis-regulated pathways with validation by molecular analysis.CytoTDP fish have early larval phenotypes resembling clinical features of ALS such as progressive motor defects, neurodegeneration and muscle atrophy. Taking advantage of zebrafish's embryonic development that solely relys on yolk usage until 5 days post fertilization, we demonstrated that microglia proliferation and activation in the hypothalamus is independent from food intake. By comparing CytoTDP to a previously generated TDP-43 knockout line, transcriptomic analyses revealed that mis-localization of endogenous TDP-43, rather than TDP-43 nuclear loss of function, leads to early onset metabolic dysfunction.The new TDP-43 model mimics the ALS/FTLD hallmark of progressive motor dysfunction. Our results suggest that functional deficits of the hypothalamus, the metabolic regulatory center, might be the primary cause of weight loss in ALS patients. Cytoplasmic gain of function of endogenous TDP-43 leads to metabolic dysfunction in vivo that are reminiscent of early ALS clinical non-motor metabolic alterations. Thus, the CytoTDP zebrafish model offers a unique opportunity to identify mis-regulated targets for therapeutic intervention early in disease progression. |
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| 650 | _ | 7 | |a ALS |2 Other |
| 650 | _ | 7 | |a Animal model |2 Other |
| 650 | _ | 7 | |a Hypothalamus |2 Other |
| 650 | _ | 7 | |a Metabolic dysfunction |2 Other |
| 650 | _ | 7 | |a Neurodegeneration |2 Other |
| 650 | _ | 7 | |a TDP-43 |2 Other |
| 650 | _ | 7 | |a Zebrafish |2 Other |
| 650 | _ | 7 | |a DNA-Binding Proteins |2 NLM Chemicals |
| 650 | _ | 7 | |a Zebrafish Proteins |2 NLM Chemicals |
| 650 | _ | 7 | |a Tardbp protein, zebrafish |2 NLM Chemicals |
| 650 | _ | 2 | |a Animals |2 MeSH |
| 650 | _ | 2 | |a Zebrafish |2 MeSH |
| 650 | _ | 2 | |a Amyotrophic Lateral Sclerosis: metabolism |2 MeSH |
| 650 | _ | 2 | |a Amyotrophic Lateral Sclerosis: pathology |2 MeSH |
| 650 | _ | 2 | |a Amyotrophic Lateral Sclerosis: genetics |2 MeSH |
| 650 | _ | 2 | |a DNA-Binding Proteins: metabolism |2 MeSH |
| 650 | _ | 2 | |a DNA-Binding Proteins: genetics |2 MeSH |
| 650 | _ | 2 | |a Disease Models, Animal |2 MeSH |
| 650 | _ | 2 | |a Motor Neurons: metabolism |2 MeSH |
| 650 | _ | 2 | |a Motor Neurons: pathology |2 MeSH |
| 650 | _ | 2 | |a Zebrafish Proteins: metabolism |2 MeSH |
| 650 | _ | 2 | |a Zebrafish Proteins: genetics |2 MeSH |
| 650 | _ | 2 | |a Animals, Genetically Modified |2 MeSH |
| 650 | _ | 2 | |a Neuromuscular Junction: metabolism |2 MeSH |
| 650 | _ | 2 | |a Neuromuscular Junction: pathology |2 MeSH |
| 700 | 1 | _ | |a Hruscha, Alexander |0 P:(DE-2719)2009882 |b 1 |u dzne |
| 700 | 1 | _ | |a Pan, Chenchen |b 2 |
| 700 | 1 | _ | |a Schifferer, Martina |0 P:(DE-2719)2812260 |b 3 |u dzne |
| 700 | 1 | _ | |a Schmidt, Michael K |b 4 |
| 700 | 1 | _ | |a Nuscher, Brigitte |b 5 |
| 700 | 1 | _ | |a Giera, Martin |b 6 |
| 700 | 1 | _ | |a Kostidis, Sarantos |b 7 |
| 700 | 1 | _ | |a Burhan, Özge |0 P:(DE-2719)2812704 |b 8 |u dzne |
| 700 | 1 | _ | |a van Bebber, Frauke |0 P:(DE-2719)9000319 |b 9 |u dzne |
| 700 | 1 | _ | |a Edbauer, Dieter |0 P:(DE-2719)2231621 |b 10 |u dzne |
| 700 | 1 | _ | |a Arzberger, Thomas |0 P:(DE-2719)2811333 |b 11 |u dzne |
| 700 | 1 | _ | |a Haass, Christian |0 P:(DE-2719)2202037 |b 12 |u dzne |
| 700 | 1 | _ | |a Schmid, Bettina |0 P:(DE-2719)2241638 |b 13 |e Last author |
| 773 | _ | _ | |a 10.1186/s13024-024-00735-7 |g Vol. 19, no. 1, p. 50 |0 PERI:(DE-600)2244557-2 |n 1 |p 50 |t Molecular neurodegeneration |v 19 |y 2024 |x 1750-1326 |
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