Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com

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! # Ola via Alexandros G.Sfakianakis on Inoreader

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Τετάρτη 19 Δεκεμβρίου 2018

The orphan nuclear receptor NR4A1 promotes FcεRI‐stimulated mast cell activation and anaphylaxis by counteracting the inhibitory LKB1/AMPK axis

Abstract

Background

NR4A1, an orphan nuclear receptor, has been implicated in several biological events such as metabolism, apoptosis, and inflammation. Recent studies indicate a potential role for NR4A1in mast cells, yet its role in allergic responses remains largely unknown.

Objectives

The aim of this study was to clarify the role of NR4A1in mast cell activation and anaphylaxis.

Methods

To evaluate the function of NR4A1in mast cells, the impacts of siRNA knockdown, gene knockout, adenoviral overexpression, and pharmacological inhibition of NR4A1on FcεRI signaling and effector functions in mouse bone marrow‐derived mast cells (BMMCs) in vitro and on anaphylactic responses in vivo were evaluated.

Results

Knockdown or knockout of NR4A1 markedly suppressed degranulation and lipid mediator production by FcεRI‐crosslinked BMMCs, while its overexpression augmented these responses. Treatment with a NR4A1 antagonist also blocked mast cell activation to a similar extent as NR4A1 knockdown or knockout. Moreover, mast cell‐specific NR4A1‐deficient mice displayed dampened anaphylactic responses in vivo. Mechanistically, NR4A1 promoted FcεRI signaling by counteracting the liver kinase B1 (LKB1)/AMP‐activated protein kinase (AMPK) axis. Following FcεRI crosslinking, NR4A1 bound to the LKB1/AMPK complex and sequestered it in the nucleus, thereby promoting FcεRI downstream signaling pathways. Silencing or knockout of LKB1/AMPK largely abrogated the effect of NR4A1 on mast cell activation. Additionally, NR4A1 facilitated Syk activation independently of LKB1/AMPK.

Conclusions

NR4A1 positively regulates mast cell activation by antagonizing the LKB1‐AMPK‐dependent negative regulatory axis. This finding may provide a novel therapeutic strategy for the development of anti‐allergic compounds.

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