1. Academic Validation
  2. Mast cells Initiate Type 2 Inflammation via Tryptase Released by MRGPRX2/MrgprB2 Activation in Atopic Dermatitis

Mast cells Initiate Type 2 Inflammation via Tryptase Released by MRGPRX2/MrgprB2 Activation in Atopic Dermatitis

  • J Invest Dermatol. 2023 Jul 21;S0022-202X(23)02422-3. doi: 10.1016/j.jid.2023.06.201.
Tao Jia 1 Delu Che 2 Yi Zheng 1 Huan Zhang 1 Yaxiang Li 1 Tong Zhou 1 Bin Peng 1 Xueshan Du 1 Longfei Zhu 1 Jingang An 1 Songmei Geng 3
Affiliations

Affiliations

  • 1 Department of Dermatology, Northwest Hospital, The Second Hospital Affiliated to Xi'an Jiaotong University, Xi'an, Shaanxi, China.
  • 2 Department of Dermatology, Northwest Hospital, The Second Hospital Affiliated to Xi'an Jiaotong University, Xi'an, Shaanxi, China; Center for Dermatology Disease, Precision Medical Institute, Xi'an, China.
  • 3 Department of Dermatology, Northwest Hospital, The Second Hospital Affiliated to Xi'an Jiaotong University, Xi'an, Shaanxi, China. Electronic address: gengsongmei73@163.com.
Abstract

Atopic dermatitis (AD) is a common chronic inflammatory skin disease characterized by T-helper 2 (Th2) inflammation as the core pathogenic mechanism. MRGPRX2 plays a key role in non-histamine allergies and neuroimmune mechanisms in chronic inflammatory dermatitis. However, the role of MRGPRX2 in AD and the development of type 2 inflammation is not yet clear. This study aimed to define the role of MRGPRX2 in type 2 inflammation development and cytokine release in AD, by determining its levels in patients with AD and healthy controls. Furthermore, MrgprB2 conditional knockout (MrgprB2-/-) and wildtype (WT) mice were used to construct an MC903 induced AD mouse model to observe skin inflammation and cytokine release. Tryptase and its antagonist were applied separately to MrgprB2-/- AD and WT AD mice to confirm the role of the MrgprB2-tryptase axis in the development of type 2 inflammation in AD. We found that AD severity and type 2 cytokine levels were not associated with IgE levels but were associated with MRGPRX2/MrgprB2 expression. MrgprB2-/- AD mice showed milder phenotypes and inflammatory infiltration in the skin than WT AD mice. Tryptase released by MRGPRX2/MrgprB2 activation is involved in the release of type 2 cytokines, which contribute to the inflammatory development in AD.

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