TY - JOUR
T1 - P2 Receptors as Therapeutic Targets in the Salivary Gland
T2 - From Physiology to Dysfunction
AU - Khalafalla, Mahmoud G.
AU - Woods, Lucas T.
AU - Jasmer, Kimberly J.
AU - Forti, Kevin Muñoz
AU - Camden, Jean M.
AU - Jensen, Janicke L.
AU - Limesand, Kirsten H.
AU - Galtung, Hilde K.
AU - Weisman, Gary A.
N1 - Funding Information:
This work was supported by the National Institute of Dental & Craniofacial Research grants R01DE007389 and R01DE023342 without their involvement in the study design, data collection, data interpretation, or manuscript preparation. This work was also supported by funding from the Faculty of Dentistry at the University of Oslo.
Publisher Copyright:
© Copyright © 2020 Khalafalla, Woods, Jasmer, Forti, Camden, Jensen, Limesand, Galtung and Weisman.
PY - 2020/3/13
Y1 - 2020/3/13
N2 - Although often overlooked in our daily lives, saliva performs a host of necessary physiological functions, including lubricating and protecting the oral cavity, facilitating taste sensation and digestion and maintaining tooth enamel. Therefore, salivary gland dysfunction and hyposalivation, often resulting from pathogenesis of the autoimmune disease Sjögren’s syndrome or from radiotherapy of the head and neck region during cancer treatment, severely reduce the quality of life of afflicted patients and can lead to dental caries, periodontitis, digestive disorders, loss of taste and difficulty speaking. Since their initial discovery in the 1970s, P2 purinergic receptors for extracellular nucleotides, including ATP-gated ion channel P2X and G protein-coupled P2Y receptors, have been shown to mediate physiological processes in numerous tissues, including the salivary glands where P2 receptors represent a link between canonical and non-canonical saliva secretion. Additionally, extracellular nucleotides released during periods of cellular stress and inflammation act as a tissue alarmin to coordinate immunological and tissue repair responses through P2 receptor activation. Accordingly, P2 receptors have gained widespread clinical interest with agonists and antagonists either currently undergoing clinical trials or already approved for human use. Here, we review the contributions of P2 receptors to salivary gland function and describe their role in salivary gland dysfunction. We further consider their potential as therapeutic targets to promote physiological saliva flow, prevent salivary gland inflammation and enhance tissue regeneration.
AB - Although often overlooked in our daily lives, saliva performs a host of necessary physiological functions, including lubricating and protecting the oral cavity, facilitating taste sensation and digestion and maintaining tooth enamel. Therefore, salivary gland dysfunction and hyposalivation, often resulting from pathogenesis of the autoimmune disease Sjögren’s syndrome or from radiotherapy of the head and neck region during cancer treatment, severely reduce the quality of life of afflicted patients and can lead to dental caries, periodontitis, digestive disorders, loss of taste and difficulty speaking. Since their initial discovery in the 1970s, P2 purinergic receptors for extracellular nucleotides, including ATP-gated ion channel P2X and G protein-coupled P2Y receptors, have been shown to mediate physiological processes in numerous tissues, including the salivary glands where P2 receptors represent a link between canonical and non-canonical saliva secretion. Additionally, extracellular nucleotides released during periods of cellular stress and inflammation act as a tissue alarmin to coordinate immunological and tissue repair responses through P2 receptor activation. Accordingly, P2 receptors have gained widespread clinical interest with agonists and antagonists either currently undergoing clinical trials or already approved for human use. Here, we review the contributions of P2 receptors to salivary gland function and describe their role in salivary gland dysfunction. We further consider their potential as therapeutic targets to promote physiological saliva flow, prevent salivary gland inflammation and enhance tissue regeneration.
KW - Sjögren’s syndrome
KW - extracellular nucleotides
KW - head and neck cancer
KW - purinergic receptors
KW - saliva
KW - salivary gland dysfunction
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U2 - 10.3389/fphar.2020.00222
DO - 10.3389/fphar.2020.00222
M3 - Review article
AN - SCOPUS:85082708170
SN - 1663-9812
VL - 11
JO - Frontiers in Pharmacology
JF - Frontiers in Pharmacology
M1 - 222
ER -