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TRPM channels as potential therapeutic targets against pro-inflammatory diseases
Affiliation:1. Institute of Biochemistry and Molecular Medicine, University of Bern, Bern, Switzerland;2. Division of Hepatology, Clinic for Oncology, Gastroenterology, Hepatology, Pulmonology and Infectious Diseases, University Hospital Leipzig, Leipzig, Germany;1. Laboratory of Pediatric Oncology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, P.O.Box 9101, 6500 HB Nijmegen, The Netherlands;2. Division of Cell Biology, The Netherlands Cancer Institute NKI-AVL, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands
Abstract: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.
Keywords:Immunity  Immune cells  signaling  Pro-inflammatory diseases  TRPM channel  α-Kinase  Calcium  Magnesium
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