Molecular Mechanisms of IL18 in Disease

被引:7
|
作者
Yamanishi, Kyosuke [1 ,2 ]
Hata, Masaki [2 ]
Gamachi, Naomi [2 ]
Watanabe, Yuko [3 ]
Yamanishi, Chiaki [3 ]
Okamura, Haruki [2 ]
Matsunaga, Hisato [1 ,2 ]
机构
[1] Hyogo Med Univ, Dept Neuropsychiat, 1-1 Mukogawa, Nishinomiya, Hyogo 6638501, Japan
[2] Hyogo Med Univ, Dept Psychoimmunol, 1-1 Mukogawa, Nishinomiya, Hyogo 6638501, Japan
[3] Hirakata Gen Hosp Dev Disorders, Hirakata, Osaka 5730122, Japan
关键词
interleukin; 18; inflammasome; diabetes; dyslipidemia; metabolic syndrome; brown adipose tissue; hippocampus; depression; learning and memory; Alzheimer's disease; FATTY LIVER-DISEASE; MUSCARINIC M-1 RECEPTOR; INTERLEUKIN-18; LEVELS; DNA-DAMAGE; ATAXIA-TELANGIECTASIA; PLASMA INTERLEUKIN-18; ALZHEIMERS-DISEASE; INSULIN-RESISTANCE; IL-18; SECRETION; PROSTATE-CANCER;
D O I
10.3390/ijms242417170
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
Interleukin 18 (IL18) was originally identified as an inflammation-induced cytokine that is secreted by immune cells. An increasing number of studies have focused on its non-immunological functions, with demonstrated functions for IL18 in energy homeostasis and neural stability. IL18 is reportedly required for lipid metabolism in the liver and brown adipose tissue. Furthermore, IL18 (Il18) deficiency in mice leads to mitochondrial dysfunction in hippocampal cells, resulting in depressive-like symptoms and cognitive impairment. Microarray analyses of Il18-/- mice have revealed a set of genes with differential expression in liver, brown adipose tissue, and brain; however, the impact of IL18 deficiency in these tissues remains uncertain. In this review article, we discuss these genes, with a focus on their relationships with the phenotypic disease traits of Il18-/- mice.
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页数:16
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