Mitochondrial One-Carbon Metabolism and Alzheimer's Disease

被引:5
作者
Yu, Yizhou [1 ]
Martins, L. Miguel [1 ]
机构
[1] Univ Cambridge, MRC Toxicol Unit, Gleeson Bldg,Tennis Court Rd, Cambridge CB2 1QR, England
基金
英国医学研究理事会;
关键词
Alzheimer's disease; mitochondria; one-carbon metabolism; folate; DNA METHYLATION; FOLIC-ACID; FOLATE TRANSPORT; LYSINE METHYLATION; SERINE CATABOLISM; DIETARY-FOLATE; CELL-GROWTH; TAU-PROTEIN; PINK1; MODEL; MOUSE MODEL;
D O I
10.3390/ijms25126302
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
Mitochondrial one-carbon metabolism provides carbon units to several pathways, including nucleic acid synthesis, mitochondrial metabolism, amino acid metabolism, and methylation reactions. Late-onset Alzheimer's disease is the most common age-related neurodegenerative disease, characterised by impaired energy metabolism, and is potentially linked to mitochondrial bioenergetics. Here, we discuss the intersection between the molecular pathways linked to both mitochondrial one-carbon metabolism and Alzheimer's disease. We propose that enhancing one-carbon metabolism could promote the metabolic processes that help brain cells cope with Alzheimer's disease-related injuries. We also highlight potential therapeutic avenues to leverage one-carbon metabolism to delay Alzheimer's disease pathology.
引用
收藏
页数:18
相关论文
共 194 条
[1]   Activation of PARP by Oxidative Stress Induced by β-Amyloid: Implications for Alzheimer's Disease [J].
Abeti, Rosella ;
Duchen, Michael R. .
NEUROCHEMICAL RESEARCH, 2012, 37 (11) :2589-2596
[2]   Cryo-EM structures of complex I from mouse heart mitochondria in two biochemically defined states [J].
Agip, Ahmed-Noor A. ;
Blaza, James N. ;
Bridges, Hannah R. ;
Viscomi, Carlo ;
Rawson, Shaun ;
Muench, Stephen P. ;
Hirst, Judy .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2018, 25 (07) :548-+
[3]   ER stress and UPR in Alzheimer's disease: mechanisms, pathogenesis, treatments [J].
Ajoolabady, Amir ;
Lindholm, Dan ;
Ren, Jun ;
Pratico, Domenico .
CELL DEATH & DISEASE, 2022, 13 (08)
[4]   Clinical Implications of Folate Transport in the Central Nervous System [J].
Alam, Camille ;
Kondo, Misaki ;
O'Connor, Deborah L. ;
Bendayan, Reina .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2020, 41 (05) :349-361
[5]   Upregulation of reduced folate carrier by vitamin D enhances brain folate uptake in mice lacking folate receptor alpha [J].
Alam, Camille ;
Aufreiter, Susanne ;
Georgiou, Constantine J. ;
Hoque, Md. Tozammel ;
Finnell, Richard H. ;
O'Connor, Deborah L. ;
Goldman, I. David ;
Bendayan, Reina .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (35) :17531-17540
[6]  
Andrews SJ., 2020, Alzheimer's Dement, V16, pe047543, DOI DOI 10.1002/ALZ.047543
[7]   Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration [J].
Araki, T ;
Sasaki, Y ;
Milbrandt, J .
SCIENCE, 2004, 305 (5686) :1010-1013
[8]   MAMMALIAN DEOXYRIBONUCLEOSIDE KINASES [J].
ARNER, ESJ ;
ERIKSSON, S .
PHARMACOLOGY & THERAPEUTICS, 1995, 67 (02) :155-186
[9]   FOLATE STATUS ASSESSMENT [J].
BAILEY, LB .
JOURNAL OF NUTRITION, 1990, 120 (11) :1508-1511
[10]   Genome-Wide DNA Methylation Differences Between Late-Onset Alzheimer's Disease and Cognitively Normal Controls in Human Frontal Cortex [J].
Bakulski, Kelly M. ;
Dolinoy, Dana C. ;
Sartor, Maureen A. ;
Paulson, Henry L. ;
Konen, John R. ;
Lieberman, Andrew P. ;
Albin, Roger L. ;
Hu, Howard ;
Rozek, Laura S. .
JOURNAL OF ALZHEIMERS DISEASE, 2012, 29 (03) :571-588