An update on the therapeutic implications of long-chain acyl-coenzyme A synthetases in nervous system diseases
Long-chain acyl-coenzyme A synthetases (ACSLs) are a family of CoA synthetases that activate fatty acid (FA) with chain lengths of 12–20 carbon atoms by forming the acyl-AMP derivative in an isozyme-specific manner. This family mainly includes five members (ACSL1, ACSL3, ACSL4, ACSL5, and ACSL6), wh...
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Published in | Frontiers in neuroscience Vol. 16; p. 1030512 |
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Abstract | Long-chain acyl-coenzyme A synthetases (ACSLs) are a family of CoA synthetases that activate fatty acid (FA) with chain lengths of 12–20 carbon atoms by forming the acyl-AMP derivative in an isozyme-specific manner. This family mainly includes five members (ACSL1, ACSL3, ACSL4, ACSL5, and ACSL6), which are thought to have specific and different functions in FA metabolism and oxidative stress of mammals. Accumulating evidence shows that the dysfunction of ACSLs is likely to affect cell proliferation and lead to metabolic diseases in multiple organs and systems through different signaling pathways and molecular mechanisms. Hence, a central theme of this review is to emphasize the therapeutic implications of ACSLs in nervous system disorders. |
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AbstractList | Long-chain acyl-coenzyme A synthetases (ACSLs) are a family of CoA synthetases that activate fatty acid (FA) with chain lengths of 12–20 carbon atoms by forming the acyl-AMP derivative in an isozyme-specific manner. This family mainly includes five members (ACSL1, ACSL3, ACSL4, ACSL5, and ACSL6), which are thought to have specific and different functions in FA metabolism and oxidative stress of mammals. Accumulating evidence shows that the dysfunction of ACSLs is likely to affect cell proliferation and lead to metabolic diseases in multiple organs and systems through different signaling pathways and molecular mechanisms. Hence, a central theme of this review is to emphasize the therapeutic implications of ACSLs in nervous system disorders. Long-chain acyl-coenzyme A synthetases (ACSLs) are a family of CoA synthetases that activate fatty acid (FA) with chain lengths of 12-20 carbon atoms by forming the acyl-AMP derivative in an isozyme-specific manner. This family mainly includes five members (ACSL1, ACSL3, ACSL4, ACSL5, and ACSL6), which are thought to have specific and different functions in FA metabolism and oxidative stress of mammals. Accumulating evidence shows that the dysfunction of ACSLs is likely to affect cell proliferation and lead to metabolic diseases in multiple organs and systems through different signaling pathways and molecular mechanisms. Hence, a central theme of this review is to emphasize the therapeutic implications of ACSLs in nervous system disorders.Long-chain acyl-coenzyme A synthetases (ACSLs) are a family of CoA synthetases that activate fatty acid (FA) with chain lengths of 12-20 carbon atoms by forming the acyl-AMP derivative in an isozyme-specific manner. This family mainly includes five members (ACSL1, ACSL3, ACSL4, ACSL5, and ACSL6), which are thought to have specific and different functions in FA metabolism and oxidative stress of mammals. Accumulating evidence shows that the dysfunction of ACSLs is likely to affect cell proliferation and lead to metabolic diseases in multiple organs and systems through different signaling pathways and molecular mechanisms. Hence, a central theme of this review is to emphasize the therapeutic implications of ACSLs in nervous system disorders. |
Author | Liao, Zhi Ling, Cong Wang, Hui Sun, Jun Chen, Chuan Qiao, Jia Wu, Zhimin |
AuthorAffiliation | 1 Department of Neurosurgery, The Third Affiliated Hospital, Sun Yat-sen University , Guangzhou, Guangdong , China 2 Department of Rehabilitation Medicine, The Third Affiliated Hospital, Sun Yat-sen University , Guangzhou, Guangdong , China |
AuthorAffiliation_xml | – name: 2 Department of Rehabilitation Medicine, The Third Affiliated Hospital, Sun Yat-sen University , Guangzhou, Guangdong , China – name: 1 Department of Neurosurgery, The Third Affiliated Hospital, Sun Yat-sen University , Guangzhou, Guangdong , China |
Author_xml | – sequence: 1 givenname: Zhimin surname: Wu fullname: Wu, Zhimin – sequence: 2 givenname: Jun surname: Sun fullname: Sun, Jun – sequence: 3 givenname: Zhi surname: Liao fullname: Liao, Zhi – sequence: 4 givenname: Jia surname: Qiao fullname: Qiao, Jia – sequence: 5 givenname: Chuan surname: Chen fullname: Chen, Chuan – sequence: 6 givenname: Cong surname: Ling fullname: Ling, Cong – sequence: 7 givenname: Hui surname: Wang fullname: Wang, Hui |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36507355$$D View this record in MEDLINE/PubMed |
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Copyright | Copyright © 2022 Wu, Sun, Liao, Qiao, Chen, Ling and Wang. Copyright © 2022 Wu, Sun, Liao, Qiao, Chen, Ling and Wang. 2022 Wu, Sun, Liao, Qiao, Chen, Ling and Wang |
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Keywords | long-chain acyl-coenzyme A synthetases (ACSLs) nervous system diseases targeted therapy fatty acid (FA) metabolism ferroptosis |
Language | English |
License | Copyright © 2022 Wu, Sun, Liao, Qiao, Chen, Ling and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 This article was submitted to Neuropharmacology, a section of the journal Frontiers in Neuroscience Edited by: Zhengwu Peng, Fourth Military Medical University, China Reviewed by: Jeroen Bogie, University of Hasselt, Belgium; Caterina Bartolacci, University of Cincinnati, United States These authors have contributed equally to this work |
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Title | An update on the therapeutic implications of long-chain acyl-coenzyme A synthetases in nervous system diseases |
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