Invertebrate genetic models of amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a common adult-onset neurodegenerative disease characterized by the progressive death of motor neurons in the cerebral cortex, brain stem, and spinal cord. The exact mechanisms underlying the pathogenesis of ALS remain unclear. The current consensus regarding t...
| 出版年: | Frontiers in Molecular Neuroscience |
|---|---|
| 主要な著者: | , |
| フォーマット: | 論文 |
| 言語: | 英語 |
| 出版事項: |
Frontiers Media S.A.
2024-03-01
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| 主題: | |
| オンライン・アクセス: | https://www.frontiersin.org/articles/10.3389/fnmol.2024.1328578/full |
| _version_ | 1850057699953213440 |
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| author | LiJun Zhou LiJun Zhou RenShi Xu RenShi Xu |
| author_facet | LiJun Zhou LiJun Zhou RenShi Xu RenShi Xu |
| author_sort | LiJun Zhou |
| collection | DOAJ |
| container_title | Frontiers in Molecular Neuroscience |
| description | Amyotrophic lateral sclerosis (ALS) is a common adult-onset neurodegenerative disease characterized by the progressive death of motor neurons in the cerebral cortex, brain stem, and spinal cord. The exact mechanisms underlying the pathogenesis of ALS remain unclear. The current consensus regarding the pathogenesis of ALS suggests that the interaction between genetic susceptibility and harmful environmental factors is a promising cause of ALS onset. The investigation of putative harmful environmental factors has been the subject of several ongoing studies, but the use of transgenic animal models to study ALS has provided valuable information on the onset of ALS. Here, we review the current common invertebrate genetic models used to study the pathology, pathophysiology, and pathogenesis of ALS. The considerations of the usage, advantages, disadvantages, costs, and availability of each invertebrate model will also be discussed. |
| format | Article |
| id | doaj-art-fb7bdde4bae747d29c10eb86fd5da22b |
| institution | Directory of Open Access Journals |
| issn | 1662-5099 |
| language | English |
| publishDate | 2024-03-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| spelling | doaj-art-fb7bdde4bae747d29c10eb86fd5da22b2025-08-20T00:23:23ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992024-03-011710.3389/fnmol.2024.13285781328578Invertebrate genetic models of amyotrophic lateral sclerosisLiJun Zhou0LiJun Zhou1RenShi Xu2RenShi Xu3Department of Neurology, National Regional Center for Neurological Diseases, Clinical College of Nanchang Medical College, Jiangxi Provincial People's Hospital, First Affiliated Hospital of Nanchang Medical College, Xiangya Hospital of Central South University Jiangxi Hospital, Nanchang, Jiangxi, ChinaMedical College of Nanchang University, Nanchang, ChinaDepartment of Neurology, National Regional Center for Neurological Diseases, Clinical College of Nanchang Medical College, Jiangxi Provincial People's Hospital, First Affiliated Hospital of Nanchang Medical College, Xiangya Hospital of Central South University Jiangxi Hospital, Nanchang, Jiangxi, ChinaMedical College of Nanchang University, Nanchang, ChinaAmyotrophic lateral sclerosis (ALS) is a common adult-onset neurodegenerative disease characterized by the progressive death of motor neurons in the cerebral cortex, brain stem, and spinal cord. The exact mechanisms underlying the pathogenesis of ALS remain unclear. The current consensus regarding the pathogenesis of ALS suggests that the interaction between genetic susceptibility and harmful environmental factors is a promising cause of ALS onset. The investigation of putative harmful environmental factors has been the subject of several ongoing studies, but the use of transgenic animal models to study ALS has provided valuable information on the onset of ALS. Here, we review the current common invertebrate genetic models used to study the pathology, pathophysiology, and pathogenesis of ALS. The considerations of the usage, advantages, disadvantages, costs, and availability of each invertebrate model will also be discussed.https://www.frontiersin.org/articles/10.3389/fnmol.2024.1328578/fullamyotrophic lateral sclerosisinvertebrate modelsyeastDrosophila melanogasterCaenorhabditis elegansSOD1 |
| spellingShingle | LiJun Zhou LiJun Zhou RenShi Xu RenShi Xu Invertebrate genetic models of amyotrophic lateral sclerosis amyotrophic lateral sclerosis invertebrate models yeast Drosophila melanogaster Caenorhabditis elegans SOD1 |
| title | Invertebrate genetic models of amyotrophic lateral sclerosis |
| title_full | Invertebrate genetic models of amyotrophic lateral sclerosis |
| title_fullStr | Invertebrate genetic models of amyotrophic lateral sclerosis |
| title_full_unstemmed | Invertebrate genetic models of amyotrophic lateral sclerosis |
| title_short | Invertebrate genetic models of amyotrophic lateral sclerosis |
| title_sort | invertebrate genetic models of amyotrophic lateral sclerosis |
| topic | amyotrophic lateral sclerosis invertebrate models yeast Drosophila melanogaster Caenorhabditis elegans SOD1 |
| url | https://www.frontiersin.org/articles/10.3389/fnmol.2024.1328578/full |
| work_keys_str_mv | AT lijunzhou invertebrategeneticmodelsofamyotrophiclateralsclerosis AT lijunzhou invertebrategeneticmodelsofamyotrophiclateralsclerosis AT renshixu invertebrategeneticmodelsofamyotrophiclateralsclerosis AT renshixu invertebrategeneticmodelsofamyotrophiclateralsclerosis |
