From mitochondria to cells to humans: Targeting bioenergetics in aging and disease

被引:2
作者
Berry, Brandon J. [1 ]
Pharaoh, Gavin A. [2 ,3 ]
Marcinek, David J. [1 ,2 ,3 ]
机构
[1] Univ Washington, Dept Lab Med & Pathol, Med Ctr, 1959 NE Pacific St, Seattle, WA 98195 USA
[2] Univ Washington, Dept Radiol, South Lake Union Campus,850 Republican St,Brotman, Seattle, WA 98109 USA
[3] Inst Stem Cell & Regenerat Med, South Lake Union Campus,850 Republican St, Brotman, Seattle, WA 98109 USA
关键词
Metabolism; Protonmotive force; Membrane potential; Respiration; Aging; Bioenergetics; LIFE-SPAN; ELEGANS;
D O I
10.1016/j.biocel.2023.106391
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In vivo control over metabolism is at the cutting edge of biomedical research. The particulars of mitochondrial function are especially important to understand in vivo to progress metabolic therapies that will be relevant for diseases of aging. Understanding the differences between how mitochondria function in vitro versus in vivo will be a necessary challenge to overcome to achieve mitochondrial medicine. In this article we outline how dis-coveries in invertebrate models will be informative for understanding the basic biology of mitochondria to streamline translation to mammals and eventually to humans. Further, we highlight examples of how what is known about mitochondria in vitro is translatable to in vivo models and, in some cases, to human diseases.
引用
收藏
页数:4
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