Hippocampal rejuvenation by a single intracerebral injection of one-carbon metabolites in C57BL6 old wild-type mice.

IF 8 1区 医学 Q1 CELL BIOLOGY Aging Cell Pub Date : 2024-10-08 DOI:10.1111/acel.14365
Alejandro Antón-Fernández, Rocío Peinado Cauchola, Félix Hernández, Jesús Ávila
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Abstract

The Izpisua-Belmonte group identified a cocktail of metabolites that promote partial reprogramming in cultured muscle cells. We tested the effect of brain injection of these metabolites in the dentate gyrus of aged wild-type mice. The dentate gyrus is a brain region essential for memory function and is extremely vulnerable to aging. A single injection of the cocktail containing four compounds (putrescine, glycine, methionine and threonine) partially reversed brain aging phenotypes and epigenetic alterations in age-associated genes. Our analysis revealed three levels: chromatin methylation, RNA sequencing, and protein expression. Functional studies complemented the previous ones, showing cognitive improvement. In summary, we report the reversal of various age-associated epigenetic changes, such as the transcription factor Zic4, and several changes related to cellular rejuvenation in the dentate gyrus (DG). These changes include increased expression of the Sox2 protein. Finally, the increases in the survival of newly generated neurons and the levels of the NMDA receptor subunit GluN2B were accompanied by improvements in both short-term and long-term memory performance. Based on these results, we propose the use of these metabolites to explore new strategies for the development of potential treatments for age-related brain diseases.

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在 C57BL6 野生型老龄小鼠脑内一次性注射一碳代谢物可使海马恢复活力。
Izpisua-Belmonte 小组发现了一种鸡尾酒代谢物,可促进培养肌肉细胞的部分重编程。我们测试了在老年野生型小鼠齿状回中注射这些代谢物的效果。齿状回是记忆功能的重要脑区,极易受到衰老的影响。单次注射含有四种化合物(腐胺、甘氨酸、蛋氨酸和苏氨酸)的鸡尾酒可部分逆转大脑衰老表型和年龄相关基因的表观遗传学改变。我们的分析揭示了三个层面:染色质甲基化、RNA 测序和蛋白质表达。功能研究补充了之前的研究,显示认知能力有所改善。总之,我们报告了与年龄相关的各种表观遗传变化的逆转,如转录因子Zic4,以及与齿状回(DG)细胞年轻化相关的一些变化。这些变化包括 Sox2 蛋白的表达增加。最后,伴随着新生成神经元存活率的提高和 NMDA 受体亚基 GluN2B 水平的提高,短期和长期记忆的表现也得到了改善。基于这些结果,我们建议利用这些代谢物探索开发潜在治疗老年性脑部疾病的新策略。
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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
期刊最新文献
Contextualizing aging clocks and properly describing biological age. CaMKIIα-TARPγ8 signaling mediates hippocampal synaptic impairment in aging. Correction to "An interpretable machine learning-based cerebrospinal fluid proteomics clock for predicting age reveals novel insights into brain aging". Hippocampal rejuvenation by a single intracerebral injection of one-carbon metabolites in C57BL6 old wild-type mice. Increased levels of extracellular matrix proteins associated with extracellular vesicles from brains of aged mice.
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