脂肪酸氧化在组织中的特殊作用。

Q1 Biochemistry, Genetics and Molecular Biology Advances in biological regulation Pub Date : 2024-12-05 DOI:10.1016/j.jbior.2024.101070
Danielle M Smith, Joseph Choi, Michael J Wolfgang
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引用次数: 0

摘要

线粒体长链脂肪酸β-氧化是一个关键的中心碳分解代谢过程。脂肪酸氧化的重要性通过与该途径中各种先天性错误相关的危及生命的疾病得到了证明。虽然先天性缺陷显示出脂肪酸氧化的多系统需求,但从这些酶缺乏的临床表现来看,尚不清楚该途径的组织特异性作用与继发性全身效应相比。为了了解脂肪酸氧化对系统生理的细胞或组织特异性贡献,在小鼠中使用条件敲除来确定不同细胞类型对脂肪酸氧化的需求。这产生了许多令人惊讶的结果,有时与这种代谢途径的规范观点背道而驰。条件敲除的严谨性也为先前利用体外细胞系或具有可疑特异性的小分子抑制剂的研究提供了清晰度。在这里,我们将总结目前使用肉碱棕榈酰基转移酶小鼠模型的研究,以确定长链线粒体脂肪酸β-氧化的组织特异性作用和需求。
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Tissue specific roles of fatty acid oxidation.

Mitochondrial long chain fatty acid β-oxidation is a critical central carbon catabolic process. The importance of fatty acid oxidation is made evident by the life-threatening disease associated with diverse inborn errors in the pathway. While inborn errors show multisystemic requirements for fatty acid oxidation, it is not clear from the clinical presentation of these enzyme deficiencies what the tissue specific roles of the pathway are compared to secondary systemic effects. To understand the cell or tissue specific contributions of fatty acid oxidation to systemic physiology, conditional knockouts in mice have been employed to determine the requirements of fatty acid oxidation in disparate cell types. This has produced a host of surprising results that sometimes run counter to the canonical view of this metabolic pathway. The rigor of conditional knockouts has also provided clarity over previous research utilizing cell lines in vitro or small molecule inhibitors with dubious specificity. Here we will summarize current research using mouse models of Carnitine Palmitoyltransferases to determine the tissue specific roles and requirements of long chain mitochondrial fatty acid β-oxidation.

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来源期刊
Advances in biological regulation
Advances in biological regulation Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
8.90
自引率
0.00%
发文量
41
审稿时长
17 days
期刊最新文献
Foreword. Insights into phosphatidic acid phosphatase and its potential role as a therapeutic target. TP53 gene status can promote sensitivity and resistance to chemotherapeutic drugs and small molecule signal transduction inhibitors. Molecular basis of JAK kinase regulation guiding therapeutic approaches: Evaluating the JAK3 pseudokinase domain as a drug target. Tissue specific roles of fatty acid oxidation.
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