Vitamin D in autophagy signaling for health and diseases: Insights on potential mechanisms and future perspectives

被引:59
作者
Bhutia, Sujit Kumar [1 ]
机构
[1] Natl Inst Technol Rourkela, Dept Life Sci, Canc & Cell Death Lab, Rourkela 769008, India
关键词
Autophagy; Cancer; Inflammation; Immunity; Vitamin D; Oxidative stress; BREAST-TUMOR CELLS; 1,25-DIHYDROXYVITAMIN D-3; D DEFICIENCY; MYCOBACTERIUM-TUBERCULOSIS; 1,25-DYHYDROXYVITAMIN D-3; ACTIVATES AUTOPHAGY; CYTOTOXIC AUTOPHAGY; 25-HYDROXYVITAMIN D; REPERFUSION INJURY; OXIDATIVE STRESS;
D O I
10.1016/j.jnutbio.2021.108841
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
Vitamin D regulates the pleiotropic effect to maintain cellular homeostasis and epidemiological evidence establishes an association between vitamin D deficiency and various human diseases. Here, the role of autophagy, the cellular self-degradation process, in vitamin D-dependent function is documented in different cellular settings and discussed the molecular aspects for treating chronic inflammatory, infectious diseases, and cancer. Vitamin D activates autophagy through a genomic and non-genomic signaling pathway to influence a wide variety of physiological functions of different body organs along with bone health and calcium metabolism. Moreover, it induces autophagy as a protective mechanism to inhibit oxidative stress and apoptosis to regulate cell proliferation, differentiation, and immune modulation. Furthermore, vitamin D and its receptor regulate autophagy signaling to control inflammation and host immunity by activating antimicrobial defense mechanisms. Vitamin D has been revealed as a potent anticancer agent and induces autophagy to increase the response to radiation and chemotherapeutic drugs for potential cancer therapy. Increasing vitamin D levels in the human body through timely exposure to sunlight or vitamin D supplements could activate autophagy as part of the homeostasis mechanism to prevent multiple human diseases and aging-associated dysfunctions. (c) 2021 Elsevier Inc. All rights reserved.
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页数:14
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