1. Academic Validation
  2. Soluble epoxide hydrolase maintains steady-state lipid turnover linked with autocrine signaling in peritoneal macrophages

Soluble epoxide hydrolase maintains steady-state lipid turnover linked with autocrine signaling in peritoneal macrophages

  • iScience. 2023 Jul 27;26(8):107465. doi: 10.1016/j.isci.2023.107465.
Feng Liu 1 Xueying Diao 1 Haolun Cong 1 Eriko Suzuki 2 Keiji Hasumi 2 3 Hiroshi Takeshima 1
Affiliations

Affiliations

  • 1 Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606-8501, Japan.
  • 2 Department of Applied Biological Science, Tokyo University of Agriculture and Technology, Tokyo 183-8509, Japan.
  • 3 Division of Research and Development, TMS Co., Ltd, Tokyo 183-0023, Japan.
Abstract

Soluble Epoxide Hydrolase is a widely distributed bifunctional enzyme that contains N-terminal Phosphatase (N-phos) and C-terminal Epoxide Hydrolase (C-EH) domains. C-EH hydrolyzes anti-inflammatory epoxy-fatty acids to corresponding diols and contributes to various inflammatory conditions. However, N-phos has been poorly examined. In peritoneal macrophages, the N-phos inhibitor amino-hydroxybenzoic acid (AHBA) seemed to primarily interrupt the dephosphorylation of lysophosphatidates and broadly attenuated inflammation-related functions. AHBA activated intrinsic lysophosphatidate and thromboxane A2 receptors by altering lipid-metabolite distribution; downstream the signaling, Phospholipase C was facilitated to dampen intracellular CA2+ stores and Akt kinase (protein kinase B) was activated to presumably inhibit inflammatory gene expression. Our data suggest that N-phos maintains steady-state phospholipid turnover connecting autocrine signaling and is a prospective target for controlling inflammatory responses in macrophages.

Keywords

Biochemistry; Biological sciences; Cell biology; Immunology.

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