Distinct Pools of Non-Glycolytic Substrates Differentiate Brain Regions and Prime Region-Specific Responses of Mitochondria

被引:21
作者
Lee, Do Yup [1 ,2 ]
Xun, Zhiyin [1 ]
Platt, Virginia [1 ,3 ]
Budworth, Helen [1 ]
Canaria, Christie A. [1 ]
McMurray, Cynthia T. [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Life Sci, Berkeley, CA 94720 USA
[2] Kookmin Univ, Dept Adv Fermentat Fus Sci & Technol, Seuol, South Korea
[3] Buck Inst Res Aging, Novato, CA USA
来源
PLOS ONE | 2013年 / 8卷 / 07期
基金
美国国家卫生研究院;
关键词
CEREBRAL GLUCOSE-UTILIZATION; ENERGY-METABOLISM; OXIDATIVE STRESS; CLUSTER-ANALYSIS; HUNTINGTONS; NETWORKS; SYSTEM; ALZHEIMERS; DISEASE; CELLS;
D O I
10.1371/journal.pone.0068831
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many hereditary diseases are characterized by region-specific toxicity, despite the fact that disease-linked proteins are generally ubiquitously expressed. The underlying basis of the region-specific vulnerability remains enigmatic. Here, we evaluate the fundamental features of mitochondrial and glucose metabolism in synaptosomes from four brain regions in basal and stressed states. Although the brain has an absolute need for glucose in vivo, we find that synaptosomes prefer to respire on non-glycolytic substrates, even when glucose is present. Moreover, glucose is metabolized differently in each brain region, resulting in region-specific "signature'' pools of non-glycolytic substrates. The use of non-glycolytic resources increases and dominates during energy crisis, and triggers a marked region-specific metabolic response. We envision that disease-linked proteins confer stress on all relevant brain cells, but region-specific susceptibility stems from metabolism of non-glycolytic substrates, which limits how and to what extent neurons respond to the stress.
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页数:11
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