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Hydroquinone-induced skin irritant reaction could be achieved by activating mast cells via mas-related G protein-coupled receptor X2.

Abstract
Hydroquinone (HQ) is one of the most effective drugs to treat hyperpigmentary disorders, but often causes skin irritation in clinic. Mast cell plays an important role in contact dermatitis and triggering pseudo-allergic reactions via MRGPRX2. Whether HQ-induced skin irritant reaction through activating mast cells via MRGPRX2 remains unknown. To investigate the role of mast cells in HQ-induced skin irritant reaction and verify whether MRGPRX2 participated in the HQ effect on mast cells which contributed to the pathogenesis of skin irritant reaction, a mouse model of HQ-induced skin irritation was established to observe the local and systemic inflammation associated with mast cell receptor MrgprB2. Human mast cell LAD2 was used to verify the effect of HQ on mast cells via MRGPRX2 by knocking down with siRNA. As a result, mast cells were involved in the development of HQ-induced irritant reaction, and local inflammation is closely related to mast cell receptor MrgprB2. HQ could activate mast cells via MRGPRX2, causing changes in calcium concentration, degranulation and release of inflammatory cytokines which lead to skin irritant reaction. In conclusion, HQ-induced skin irritant reaction could be skin pseudo-allergic reactions achieved by activating mast cells via MRGPRX2.
AuthorsYi Zheng, Xueshan Du, Lei Zhang, Tao Jia, Huan Zhang, Bin Peng, Yong Hao, Zhou Tong, Delu Che, Songmei Geng
JournalExperimental dermatology (Exp Dermatol) Vol. 32 Issue 4 Pg. 436-446 (04 2023) ISSN: 1600-0625 [Electronic] Denmark
PMID36463492 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Chemical References
  • Irritants
  • hydroquinone
  • Hydroquinones
  • Receptors, G-Protein-Coupled
  • MRGPRX2 protein, human
  • Nerve Tissue Proteins
  • Receptors, Neuropeptide
Topics
  • Animals
  • Mice
  • Humans
  • Mast Cells (pathology)
  • Irritants (toxicity)
  • Hydroquinones (adverse effects)
  • Hypersensitivity
  • Receptors, G-Protein-Coupled (genetics)
  • Inflammation (pathology)
  • Dermatitis, Atopic (pathology)
  • Cell Degranulation
  • Nerve Tissue Proteins (genetics)
  • Receptors, Neuropeptide (genetics)

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