Peroxisome Proliferator-Activated Receptor-Targeted Therapies: Challenges upon Infectious Diseases

被引:18
|
作者
Kim, In Soo [1 ,2 ,3 ]
Silwal, Prashanta [4 ]
Jo, Eun-Kyeong [1 ,2 ,3 ]
机构
[1] Chungnam Natl Univ, Coll Med, Dept Microbiol, Daejeon 35015, South Korea
[2] Chungnam Natl Univ, Coll Med, Dept Med Sci, Daejeon 35015, South Korea
[3] Chungnam Natl Univ, Coll Med, Infect Control Convergence Res Ctr, Daejeon 35015, South Korea
[4] Univ Pittsburgh, Dept Orthopaed Surg, Sch Med, Pittsburgh, PA 15261 USA
基金
新加坡国家研究基金会;
关键词
peroxisome proliferator-activated receptor; infection; bacteria; virus; parasite; PPAR-GAMMA; FATTY-ACIDS; LIGAND-BINDING; LIPID BODIES; ALPHA; EXPRESSION; BETA/DELTA; INDUCTION; METABOLISM; FAMILY;
D O I
10.3390/cells12040650
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Peroxisome proliferator-activated receptors (PPARs) alpha, beta, and gamma are nuclear receptors that orchestrate the transcriptional regulation of genes involved in a variety of biological responses, such as energy metabolism and homeostasis, regulation of inflammation, cellular development, and differentiation. The many roles played by the PPAR signaling pathways indicate that PPARs may be useful targets for various human diseases, including metabolic and inflammatory conditions and tumors. Accumulating evidence suggests that each PPAR plays prominent but different roles in viral, bacterial, and parasitic infectious disease development. In this review, we discuss recent PPAR research works that are focused on how PPARs control various infections and immune responses. In addition, we describe the current and potential therapeutic uses of PPAR agonists/antagonists in the context of infectious diseases. A more comprehensive understanding of the roles played by PPARs in terms of host-pathogen interactions will yield potential adjunctive personalized therapies employing PPAR-modulating agents.
引用
收藏
页数:18
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