TRPM channels as potential therapeutic targets against pro-inflammatory diseases

被引:29
作者
Zierler, Susanna [1 ]
Hampe, Sarah [1 ]
Nadolni, Wiebke [1 ]
机构
[1] Ludwig Maximilians Univ Munchen, Walther Straub Inst Pharmacol & Toxicol, Munich, Germany
关键词
Immunity; Immune cells; signaling; Pro-inflammatory diseases; TRPM channel; alpha-Kinase; Calcium; Magnesium; MAST-CELL ACTIVATION; OPERATED CA2+ ENTRY; CATION CHANNEL; ION CHANNELS; KINASES TRPM6; SIGNAL-TRANSDUCTION; HELICOBACTER-PYLORI; OXIDATIVE STRESS; MG2+ HOMEOSTASIS; INNATE IMMUNITY;
D O I
10.1016/j.ceca.2017.05.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The immune system protects our body against foreign pathogens. However, if it overshoots or turns against itself, pro-inflammatory diseases, such as rheumatoid arthritis, inflammatory bowel disease, or diabetes develop. Ions, the most basic signaling molecules, shape intracellular signaling cascades resulting in immune cell activation and subsequent immune responses. Mutations in ion channels required for calcium signaling result in human immunodeficiencies and highlight those ion channels as valued targets for therapies against pro-inflammatory diseases. Signaling pathways regulated by melastatin-like transient receptor potential (TRPM) cation channels also play crucial roles in calcium signaling and leukocyte physiology, affecting phagocytosis, degranulation, chemokine and cytokine expression, chemotaxis and invasion, as well as lymphocyte development and proliferation. Therefore, this review discusses their regulation, possible interactions and whether they can be exploited as targets for therapeutic approaches to pro-inflammatory diseases. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:105 / 115
页数:11
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