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March 16, 2026Poultry Science2 citationsOpen Access

Mechanism of Scutellaria baicalensis Extracellular Vesicles in Attenuating Mycoplasma gallisepticum-induced Inflammation via TRPC1 - STIM1/ORAI1 Channel Inhibition

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FXFangbing XuLBLige BaoYYYecheng Yao

Key Points

  • This study aims to explore how Scutellaria baicalensis extracellular vesicles modulate inflammation caused by Mycoplasma gallisepticum through calcium signaling pathways.
  • Characterization of Scutellaria baicalensis extracellular vesicles
  • In vitro and in vivo infection models using Mycoplasma gallisepticum
  • Employing non-targeted metabolomics, qRT-PCR, Western Blot, and calcium imaging
  • siRNA-mediated STIM1 knockdown and plasmid overexpression experiments
  • SEVs significantly downregulated TRPC1, STIM1, and ORAI1 molecules involved in calcium signaling
  • Treatment with SEVs reduced pro-inflammatory cytokine levels
  • SEVs restored calcium homeostasis and inhibited NF-κB signaling
  • Non-targeted metabolomics highlighted the regulation of metabolic pathways related to calcium signaling by SEVs

Abstract

The infection caused by Mycoplasma gallisepticum ( MG ) has had a significant impact on the poultry industry. Scutellaria baicalensis extract has shown great potential in anti-MG infection, but the role and mechanism of its extracellular vesicles ( EVs ) remain unexplored. The aim of this study is to investigate the potential mechanism of Scutellaria baicalensis derived extracellular vesicles ( SEVs ) against MG, especially by regulating TRPC1-STIM1/ORAI1 signaling pathway, which is a key component of store-operated calcium entry ( SOCE ). SEVs were obtained from Scutellaria baicalensis and subsequently subjected to characterization. Through in vitro and in vivo MG infection models, experimental techniques including non-targeted metabolomics, qRT-PCR, Western Blot and Fluo-4 AM calcium imaging were employed. Additionally, synergistic and antagonistic effects were demonstrated via siRNA-mediated STIM1 knockdown and plasmid overexpression experiments to validate its pivotal role. Non-targeted metabolomics analysis showed that SEVs treatment regulated metabolic pathways related to calcium signaling pathway compared with MG-infected group, which aided our study to determine that SEVs may affect inflammatory injury by affecting calcium signaling. The results of molecular experiments showed that SEVs markedly downregulated SOCE molecules (TRPC1, STIM1 and ORAI1) at mRNA and protein levels, effectively suppressing MG-induced abnormal intracellular calcium influx and reducing pro-inflammatory cytokine production. : SEVs alleviate MG-induced inflammation through the TRPC1-STIM1/ORAI1 pathway, restoring calcium homeostasis and inhibiting NF-κB signaling and cytokine release. : This study reveals a novel mechanism by which plant-derived exosome-like nanoparticles ( PELNs ) exert anti-inflammatory effects, highlighting their potential as a natural nanotherapeutic strategy for controlling MG infection in poultry.

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Cite This Study

Xu et al. (2026) studied this question.

synapsesocial.com/papers/69b79dce8166e15b153aafc2https://doi.org/10.1016/j.psj.2026.106773
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