The Role of Osteoclast Energy Metabolism in the Occurrence and Development of Osteoporosis

被引:117
作者
Da, Wacili [1 ]
Tao, Lin [1 ]
Zhu, Yue [1 ]
机构
[1] China Med Univ, Dept Orthoped, Hosp 1, Shenyang, Peoples R China
关键词
osteoclasts; osteoporosis; energy metabolism; bone homeostasis; bone resorption; BONE HOMEOSTASIS; HYPOXIA; AUTOPHAGY; TRANSPORTERS; MECHANISMS; STIMULATOR; BINDING;
D O I
10.3389/fendo.2021.675385
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In recent decades, the mechanism underlying bone metabolic disorders based on energy metabolism has been heavily researched. Bone resorption by osteoclasts plays an important role in the occurrence and development of osteoporosis. However, the mechanism underlying the osteoclast energy metabolism disorder that interferes with bone homeostasis has not been determined. Bone resorption by osteoclasts is a process that consumes large amounts of adenosine triphosphate (ATP) produced by glycolysis and oxidative phosphorylation. In addition to glucose, fatty acids and amino acids can also be used as substrates to produce energy through oxidative phosphorylation. In this review, we summarize and analyze the energy-based phenotypic changes, epigenetic regulation, and coupling with systemic energy metabolism of osteoclasts during the development and progression of osteoporosis. At the same time, we propose a hypothesis, the compensatory recovery mechanism (involving the balance between osteoclast survival and functional activation), which may provide a new approach for the treatment of osteoporosis.
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页数:18
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共 173 条
[1]   ACTIVATION OF THE NADPH OXIDASE INVOLVES THE SMALL GTP-BINDING PROTEIN P21RAC1 [J].
ABO, A ;
PICK, E ;
HALL, A ;
TOTTY, N ;
TEAHAN, CG ;
SEGAL, AW .
NATURE, 1991, 353 (6345) :668-670
[2]   Reactive Oxygen Species in Osteoclast Differentiation and Possible Pharmaceutical Targets of ROS-Mediated Osteoclast Diseases [J].
Agidigbi, Taiwo Samuel ;
Kim, Chaekyun .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (14)
[3]   Accelerated Lactate Dehydrogenase Activity Potentiates Osteoclastogenesis via NFATc1 Signaling [J].
Ahn, Heejin ;
Lee, Kyunghee ;
Kim, Jin Man ;
Kwon, So Hyun ;
Lee, Seoung Hoon ;
Lee, Soo Young ;
Jeong, Daewon .
PLOS ONE, 2016, 11 (04)
[4]   Regulation of human osteoclast differentiation by thioredoxin binding protein-2 and redox-sensitive signaling [J].
Aitken, CJ ;
Hodge, JM ;
Nishinaka, Y ;
Vaughan, T ;
Yodoi, JJ ;
Day, CJ ;
Morrison, NA ;
Nicholson, GC .
JOURNAL OF BONE AND MINERAL RESEARCH, 2004, 19 (12) :2057-2064
[5]   Unraveling the role of FoxOs in bone-Insights from mouse models [J].
Almeida, Maria .
BONE, 2011, 49 (03) :319-327
[6]   Characterization of Functional Reprogramming during Osteoclast Development Using Quantitative Proteomics and mRNA Profiling [J].
An, Eunkyung ;
Narayanan, Manikandan ;
Manes, Nathan P. ;
Nita-Lazar, Aleksandra .
MOLECULAR & CELLULAR PROTEOMICS, 2014, 13 (10) :2687-2704
[7]   Metabolic properties of the osteoclast [J].
Arnett, Timothy R. ;
Orriss, Isabel R. .
BONE, 2018, 115 :25-30
[8]   Acidosis, hypoxia and bone [J].
Arnett, Timothy R. .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2010, 503 (01) :103-109
[9]   Hypoxia is a major stimulator of osteoclast formation and bone resorption [J].
Arnett, TR ;
Gibbons, DC ;
Utting, JC ;
Orriss, IR ;
Hoebertz, A ;
Rosendaal, M ;
Meghji, S .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 196 (01) :2-8
[10]   Epigenetic Regulators Involved in Osteoclast Differentiation [J].
Astleford, Kristina ;
Campbell, Emily ;
Norton, Andrew ;
Mansky, Kim C. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (19) :1-15