Iron homeostasis and organismal aging

被引:83
|
作者
Zeidan, Rola S. [1 ]
Han, Sung Min [1 ]
Leeuwenburgh, Christiaan [1 ]
Xiao, Rui [1 ,2 ,3 ]
机构
[1] Univ Florida, Inst Aging, Dept Aging & Geriatr Res, POB 100143, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Dept Pharmacol & Therapeut, Gainesville, FL 32610 USA
[3] Univ Florida, Ctr Smell & Taste, Gainesville, FL 32610 USA
关键词
Iron; Aging; Longevity; Homeostasis; Human diseases; C; elegans; Drosophila; RECEPTOR-MEDIATED ENDOCYTOSIS; HYPOXIA-INDUCIBLE FACTORS; GENOME-WIDE ASSOCIATION; TRANSFERRIN-BOUND IRON; REGULATORY PROTEINS; RESPONSIVE ELEMENT; CELL-DEATH; HEREDITARY HEMOCHROMATOSIS; MATRIPTASE-2; TMPRSS6; OXIDATIVE STRESS;
D O I
10.1016/j.arr.2021.101510
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Iron is indispensable for normal body functions across species because of its critical roles in red blood cell function and many essential proteins and enzymes required for numerous physiological processes. Regulation of iron homeostasis is an intricate process involving multiple modulators at the systemic, cellular, and molecular levels. Interestingly, emerging evidence has demonstrated that many modulators of iron homeostasis contribute to organismal aging and longevity. On the other hand, the age-related dysregulation of iron homeostasis is often associated with multiple age-related pathologies including bone resorption and neurodegenerative diseases such as Alzheimer's disease. Thus, a thorough understanding on the interconnections between systemic and cellular iron balance and organismal aging may help decipher the etiologies of multiple age-related diseases, which could ultimately lead to developing therapeutic strategies to delay aging and treat various age-related diseases. Here we present the current understanding on the mechanisms of iron homeostasis. We also discuss the impacts of aging on iron homeostatic processes and how dysregulated iron metabolism may affect aging and organismal longevity.
引用
收藏
页数:14
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