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KMID : 1141520230380060739
Endocrinology and Metabolism
2023 Volume.38 No. 6 p.739 ~ p.749
Phospholipase C-¥ã as a Potential Therapeutic Target for Graves¡¯ Orbitopathy
Roh Tae-Hoon

Chae Min-Kyung
Ko Jae-Sang
Don O. Kikkawa
Jang Sun-Young
Yoon Jin-Sook
Abstract
Background: Phospholipase C-¥ã (PLC-¥ã) plays a crucial role in immune responses and is related to the pathogenesis of various inflammatory disorders. In this study, we investigated the role of PLC-¥ã and the therapeutic effect of the PLC-specific inhibitor U73122 using orbital fibroblasts from patients with Graves¡¯ orbitopathy (GO).

Methods: The expression of phospholipase C gamma 1 (PLCG1) and phospholipase C gamma 2 (PLCG2) was evaluated using polymerase chain reaction in GO and normal orbital tissues/fibroblasts. The primary cultures of orbital fibroblasts were treated with non-toxic concentrations of U73122 with or without interleukin (IL)-1¥â to determine its therapeutic efficacy. The proinflammatory cytokine levels and activation of downstream signaling molecules were determined using Western blotting.

Results: PLCG1 and PLCG2 mRNA expression was significantly higher in GO orbital tissues than in controls (P<0.05). PLCG1 and PLCG2 mRNA expression was significantly increased (P<0.05) in IL-1¥â, tumor necrosis factor-¥á, and a cluster of differentiation 40 ligand-stimulated GO fibroblasts. U73122 significantly inhibited the IL-1¥â-induced expression of proinflammatory molecules, including IL-6, IL-8, monocyte chemoattractant protein-1, cyclooxygenase-2, and intercellular adhesion molecule-1 (ICAM-1), and phosphorylated protein kinase B (p-Akt) and p38 (p-p38) kinase in GO fibroblasts, whereas it inhibited IL-6, IL-8, and ICAM-1, and p-Akt and c-Jun N-terminal kinase (p-JNK) in normal fibroblasts (P<0.05).

Conclusion: PLC-¥ã-inhibiting U73122 suppressed the production of proinflammatory cytokines and the phosphorylation of Akt and p38 kinase in GO fibroblasts. This study indicates the implications of PLC-¥ã in GO pathogenesis and its potential as a therapeutic target for GO.
KEYWORD
Phospholipase C gamma, Graves ophthalmopathy, U73122, Proinflammatory cytokines, Inflammation, Orbital fibroblasts
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