Please use this identifier to cite or link to this item: https://doi.org/10.1126/sciadv.aav0216
Title: MRGPR-mediated activation of local mast cells clears cutaneous bacterial infection and protects against reinfection
Authors: Arifuzzaman, M.
Mobley, Y.R.
Choi, H.W.
Bist, P. 
Salinas, C.A.
Brown, Z.D.
Chen, S.L. 
Staats, H.F.
Abraham, S.N. 
Issue Date: 2019
Publisher: American Association for the Advancement of Science
Citation: Arifuzzaman, M., Mobley, Y.R., Choi, H.W., Bist, P., Salinas, C.A., Brown, Z.D., Chen, S.L., Staats, H.F., Abraham, S.N. (2019). MRGPR-mediated activation of local mast cells clears cutaneous bacterial infection and protects against reinfection. Science Advances 5 (1) : eaav0216. ScholarBank@NUS Repository. https://doi.org/10.1126/sciadv.aav0216
Rights: Attribution-NonCommercial 4.0 International
Abstract: Mast cells (MCs) are strategically distributed at barrier sites and prestore various immunocyte-recruiting cytokines, making them ideal targets for selective activation to treat peripheral infections. Here, we report that topical treatment with mastoparan, a peptide MC activator (MCA), enhances clearance of Staphylococcus aureus from infected mouse skins and accelerates healing of dermonecrotic lesions. Mastoparan functions by activating connective tissue MCs (CTMCs) via the MRGPRX2 (Mas-related G protein-coupled receptor member X2) receptor. Peripheral CTMC activation, in turn, enhances recruitment of bacteria-clearing neutrophils and wound-healing CD301b + dendritic cells. Consistent with MCs playing a master coordinating role, MC activation also augmented migration of various antigen-presenting dendritic cells to draining lymph nodes, leading to stronger protection against a second infection challenge. MCAs therefore orchestrate both the innate and adaptive immune arms, which could potentially be applied to combat peripheral infections by a broad range of pathogens. Copyright © 2019 The Authors, some rights reserved.
Source Title: Science Advances
URI: https://scholarbank.nus.edu.sg/handle/10635/210053
ISSN: 2375-2548
DOI: 10.1126/sciadv.aav0216
Rights: Attribution-NonCommercial 4.0 International
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