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Published on: July 26, 2017
Pharmacology of T2R Mediated Host-Microbe Interactions
Manoj Reddy Medapati1,2, Anjali Y Bhagirath1,2, Nisha Singh1,2
1Manitoba Chemosensory Biology Research Group, Department of Oral Biology, Dr. Gerald Niznick College of Dentistry, University of Manitoba, Winnipeg, MB, Canada.
Abstract:
Bitter taste receptors (T2Rs) belong to the G protein-coupled receptor superfamily. Humans express 25 T2Rs that are known to detect several bitter compounds including bacterial quorum sensing molecules (QSM). Primarily found to be key receptors for bitter sensation T2Rs are known to play an important role in mediating innate immune responses in oral and extraoral tissues. Several studies have led to identification of Gram-negative and Gram-positive bacterial QSMs as agonists for T2Rs in airway epithelial cells and immune cells. However, the pharmacological characterization for many of the QSM-T2R interactions remains poorly defined. In this chapter, we discuss the extraoral roles including localization of T2Rs in extracellular vesicles, molecular pharmacology of QSM-T2R interactions, role of T2Rs in mediating innate immune responses, and some of the challenges in understanding T2R pharmacology.
Insights
Bitter taste receptors (T2Rs) detect bacterial quorum sensing molecules (QSM) and play a role in innate immunity. Further research is needed to fully understand these QSM-T2R interactions and their pharmacological properties.
Area of Science:
- Molecular biology
- Immunology
- Pharmacology
Background:
- Bitter taste receptors (T2Rs) are G protein-coupled receptors involved in detecting bitter compounds.
- Humans have 25 T2Rs that can detect bacterial quorum sensing molecules (QSM).
- T2Rs are crucial for bitter taste sensation and innate immune responses in various tissues.
Purpose of the Study:
- To discuss the extraoral roles of T2Rs.
- To explore the molecular pharmacology of QSM-T2R interactions.
- To highlight challenges in understanding T2R pharmacology.
Main Methods:
- Literature review and discussion of existing studies on T2Rs and QSM.
- Analysis of T2R localization in extracellular vesicles.
- Examination of QSM-T2R interactions in immune and airway epithelial cells.
Main Results:
- Bacterial QSMs from Gram-negative and Gram-positive bacteria activate T2Rs in immune and airway cells.
- T2Rs are found in extracellular vesicles, suggesting novel signaling pathways.
- The pharmacological characterization of many QSM-T2R interactions is still poorly defined.
Conclusions:
- T2Rs have significant extraoral roles beyond taste perception, particularly in innate immunity.
- Understanding QSM-T2R interactions is critical for elucidating immune responses.
- Further pharmacological studies are essential to overcome current challenges in T2R research.
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