Suppr超能文献

我们所说的“衰老”是什么意思?果蝇研究揭示的问题和观点。

What do we mean by "aging"? Questions and perspectives revealed by studies in Drosophila.

机构信息

National Institute of Neurological Disorders and Stroke, National Institutes of Health (NIH), Bethesda, MD, United States; Interdisciplinary Program in Neuroscience, Georgetown University, Washington DC, United States; College of Medicine, University of Kentucky, Lexington, KY, United States.

National Institute of Neurological Disorders and Stroke, National Institutes of Health (NIH), Bethesda, MD, United States.

出版信息

Mech Ageing Dev. 2023 Jul;213:111839. doi: 10.1016/j.mad.2023.111839. Epub 2023 Jun 23.

Abstract

What is the nature of aging, and how best can we study it? Here, using a series of questions that highlight differing perspectives about the nature of aging, we ask how data from Drosophila melanogaster at the organismal, tissue, cellular, and molecular levels shed light on the complex interactions among the phenotypes associated with aging. Should aging be viewed as an individual's increasing probability of mortality over time or as a progression of physiological states? Are all age-correlated changes in physiology detrimental to vigor or are some compensatory changes that maintain vigor? Why do different age-correlated functions seem to change at different rates in a single individual as it ages? Should aging be considered as a single, integrated process across the scales of biological resolution, from organismal to molecular, or must we consider each level of biological scale as a separate, distinct entity? Viewing aging from these differing perspectives yields distinct but complementary interpretations about the properties and mechanisms of aging and may offer a path through the complexities related to understanding the nature of aging.

摘要

衰老的本质是什么,我们应该如何最好地研究它呢?在这里,我们通过一系列的问题,从不同的角度探讨了衰老的本质,这些问题强调了衰老相关表型之间复杂的相互作用,我们还探讨了利用黑腹果蝇在机体、组织、细胞和分子水平上的数据,如何阐明这些相互作用。衰老是否应该被视为个体随时间推移而死亡概率的增加,或者被视为一系列生理状态的进展?所有与年龄相关的生理变化都对活力有害,还是有些补偿性变化可以维持活力?为什么随着个体年龄的增长,不同的与年龄相关的功能在单个个体中似乎以不同的速度发生变化?衰老是否应该被视为跨越生物分辨率尺度(从机体到分子)的单一、综合过程,还是我们必须将每个生物学尺度的水平视为一个单独的、不同的实体?从这些不同的角度看待衰老,可以对衰老的性质和机制产生独特但互补的解释,并为理解衰老的本质提供一条途径,帮助我们应对相关的复杂性。

相似文献

1
What do we mean by "aging"? Questions and perspectives revealed by studies in Drosophila.
Mech Ageing Dev. 2023 Jul;213:111839. doi: 10.1016/j.mad.2023.111839. Epub 2023 Jun 23.
2
Circadian regulation of metabolism and healthspan in Drosophila.
Free Radic Biol Med. 2018 May 1;119:62-68. doi: 10.1016/j.freeradbiomed.2017.12.025. Epub 2017 Dec 19.
3
Review of genetic investigations into the aging processes of Drosophila.
J Am Geriatr Soc. 1989 Aug;37(8):757-73. doi: 10.1111/j.1532-5415.1989.tb02240.x.
4
Water balance and cation levels in Drosophila: can early physiological decline predict aging and longevity?
J Gerontol A Biol Sci Med Sci. 2006 Feb;61(2):146-52. doi: 10.1093/gerona/61.2.146.
5
Dissecting the genetics of longevity in Drosophila melanogaster.
Fly (Austin). 2009 Jan-Mar;3(1):29-38. doi: 10.4161/fly.3.1.7771. Epub 2009 Jan 6.
6
Patterns of physiological decline due to age and selection in Drosophila melanogaster.
Evolution. 2016 Nov;70(11):2550-2561. doi: 10.1111/evo.13065. Epub 2016 Oct 18.
7
JNK Signaling in Aging and Longevity.
Int J Mol Sci. 2021 Sep 6;22(17):9649. doi: 10.3390/ijms22179649.
8
Age-related change in γH2AX of Drosophila muscle: its significance as a marker for muscle damage and longevity.
Biogerontology. 2015 Aug;16(4):503-16. doi: 10.1007/s10522-015-9573-0. Epub 2015 Apr 10.
9
Advances in age-old questions.
Fly (Austin). 2008 May-Jun;2(3):149-51. doi: 10.4161/fly.6381. Epub 2008 May 29.
10
Endocrine Regulation of Aging in the Fruit Fly .
Zoolog Sci. 2024 Feb;41(1):4-13. doi: 10.2108/zs230056.

引用本文的文献

本文引用的文献

1
Aging Fly Cell Atlas identifies exhaustive aging features at cellular resolution.
Science. 2023 Jun 16;380(6650):eadg0934. doi: 10.1126/science.adg0934.
2
Distinct longevity mechanisms across and within species and their association with aging.
Cell. 2023 Jun 22;186(13):2929-2949.e20. doi: 10.1016/j.cell.2023.05.002. Epub 2023 Jun 3.
3
Cell-type-specific aging clocks to quantify aging and rejuvenation in neurogenic regions of the brain.
Nat Aging. 2023 Jan;3(1):121-137. doi: 10.1038/s43587-022-00335-4. Epub 2022 Dec 19.
4
A complex systems approach to aging biology.
Nat Aging. 2022 Jul;2(7):580-591. doi: 10.1038/s43587-022-00252-6. Epub 2022 Jul 20.
5
MicroRNAs in Age-Related Proteostasis and Stress Responses.
Noncoding RNA. 2023 Apr 13;9(2):26. doi: 10.3390/ncrna9020026.
6
Expression of retrotransposons contributes to aging in Drosophila.
Genetics. 2023 May 26;224(2). doi: 10.1093/genetics/iyad073.
7
Aging mechanisms-A perspective mostly from .
Adv Genet (Hoboken). 2020 Aug 10;1(1):e10026. doi: 10.1002/ggn2.10026. eCollection 2020 Dec.
8
Hallmarks of aging: An expanding universe.
Cell. 2023 Jan 19;186(2):243-278. doi: 10.1016/j.cell.2022.11.001. Epub 2023 Jan 3.
9
Discovery and Visualization of Age-Dependent Patterns in the Diurnal Transcriptome of Drosophila.
J Circadian Rhythms. 2022 Dec 8;20:1. doi: 10.5334/jcr.218. eCollection 2022.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验