TY - JOUR
T1 - Ketogenic diet uncovers differential metabolic plasticity of brain cells
AU - Düking, Tim
AU - Spieth, Lena
AU - Berghoff, Stefan A.
AU - Piepkorn, Lars
AU - Schmidke, Annika M.
AU - Mitkovski, Miso
AU - Kannaiyan, Nirmal
AU - Hosang, Leon
AU - Scholz, Patricia
AU - Shaib, Ali H.
AU - Schneider, Lennart V.
AU - Hesse, Dörte
AU - Ruhwedel, Torben
AU - Sun, Ting
AU - Linhoff, Lisa
AU - Trevisiol, Andrea
AU - Köhler, Susanne
AU - Pastor, Adrian Marti
AU - Misgeld, Thomas
AU - Sereda, Michael
AU - Hassouna, Imam
AU - Rossner, Moritz J.
AU - Odoardi, Francesca
AU - Ischebeck, Till
AU - de Hoz, Livia
AU - Hirrlinger, Johannes
AU - Jahn, Olaf
AU - Saher, Gesine
N1 - Publisher Copyright:
Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC)
PY - 2022/9/16
Y1 - 2022/9/16
N2 - To maintain homeostasis, the body, including the brain, reprograms its metabolism in response to altered nutrition or disease. However, the consequences of these challenges for the energy metabolism of the different brain cell types remain unknown. Here, we generated a proteome atlas of the major central nervous system (CNS) cell types from young and adult mice, after feeding the therapeutically relevant low-carbohydrate, high-fat ketogenic diet (KD) and during neuroinflammation. Under steady-state conditions, CNS cell types prefer distinct modes of energy metabolism. Unexpectedly, the comparison with KD revealed distinct cell type-specific strategies to manage the altered availability of energy metabolites. Astrocytes and neurons but not oligodendrocytes demonstrated metabolic plasticity. Moreover, inflammatory demyelinating disease changed the neuronal metabolic signature in a similar direction as KD. Together, these findings highlight the importance of the metabolic cross-talk between CNS cells and between the periphery and the brain to manage altered nutrition and neurological disease.
AB - To maintain homeostasis, the body, including the brain, reprograms its metabolism in response to altered nutrition or disease. However, the consequences of these challenges for the energy metabolism of the different brain cell types remain unknown. Here, we generated a proteome atlas of the major central nervous system (CNS) cell types from young and adult mice, after feeding the therapeutically relevant low-carbohydrate, high-fat ketogenic diet (KD) and during neuroinflammation. Under steady-state conditions, CNS cell types prefer distinct modes of energy metabolism. Unexpectedly, the comparison with KD revealed distinct cell type-specific strategies to manage the altered availability of energy metabolites. Astrocytes and neurons but not oligodendrocytes demonstrated metabolic plasticity. Moreover, inflammatory demyelinating disease changed the neuronal metabolic signature in a similar direction as KD. Together, these findings highlight the importance of the metabolic cross-talk between CNS cells and between the periphery and the brain to manage altered nutrition and neurological disease.
UR - http://www.scopus.com/inward/record.url?scp=85138210730&partnerID=8YFLogxK
U2 - 10.1126/sciadv.abo7639
DO - 10.1126/sciadv.abo7639
M3 - Article
C2 - 36112685
AN - SCOPUS:85138210730
SN - 2375-2548
VL - 8
JO - Science Advances
JF - Science Advances
IS - 37
M1 - eabo7639
ER -