Echinococcus granulosus sensu lato promotes osteoclast differentiation through DUSP4-MAPK signaling in osseous echinococcosis

This study reveals the molecular mechanism by which <i>Echinococcus granulosus</i> drives abnormal osteoclast activation through the DUSP4-MAPK signaling axis. Parasitic infection suppresses DUSP4 expression, relieving its negative regulation of the MAPK pathway and leading to excessive osteoclast differentiation. Restoring DUSP4 expression effectively reverses abnormal MAPK pathway activation, reducing osteoclast bone resorption activity to physiological levels. These findings not only provide new insights into the pathological mechanisms of bone destruction in osseous echinococcosis but also establish DUSP4 as a critical therapeutic target for pathological bone resorption, laying the groundwork for host-directed treatment strategies for parasitic bone diseases.

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Publication Details

Journal
Frontiers in Microbiology
Published
2025-03-19
DOI
https://doi.org/10.3389/fmicb.2025.1558603
Citations
1
Primary Topic
Parasitic infections in humans and animals
Type
article
Field-Weighted Citation Impact
1.47

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article

Echinococcus granulosus sensu lato promotes osteoclast differentiation through DUSP4-MAPK signaling in osseous echinococcosis

Chenhui Shi, Kai Xiong, Zhendong Zhang, Haohao Sun et al.
1 citations
Frontiers in Microbiology
Parasitic infections in humans and animals
1.47
article

Echinococcus granulosus sensu lato promotes osteoclast differentiation through DUSP4-MAPK signaling in osseous echinococcosis

Chenhui Shi, Kai Xiong, Zhendong Zhang, Haohao Sun, Jing Li, Sibo Wang, Yaqing Liu, Qi Li, Yiping Huang, Yi Dai, Weishan Wang
article en
1 citations

Abstract

This study reveals the molecular mechanism by which <i>Echinococcus granulosus</i> drives abnormal osteoclast activation through the DUSP4-MAPK signaling axis. Parasitic infection suppresses DUSP4 expression, relieving its negative regulation of the MAPK pathway and leading to excessive osteoclast differentiation. Restoring DUSP4 expression effectively reverses abnormal MAPK pathway activation, reducing osteoclast bone resorption activity to physiological levels. These findings not only provide new insights into the pathological mechanisms of bone destruction in osseous echinococcosis but also establish DUSP4 as a critical therapeutic target for pathological bone resorption, laying the groundwork for host-directed treatment strategies for parasitic bone diseases.

Frontiers in MicrobiologyVol. 16
Shihezi University (CN), Xi'an Honghui Hospital (CN), First Affiliated Hospital of Shihezi University Medical College (CN), Xi'an Jiaotong University (CN)
Shihezi University
Life in Land
Openalex Percentile: Top 22%
Parasitic infections in humans and animals
1.47
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Echinococcus granulosus sensu lato promotes osteoclast differentiation through DUSP4-MAPK signaling in osseous echinococcosis — Chenhui Shi, Kai Xiong, et al. · Frontiers in Microbiology (2025) | TGRS Research Map | TGRS