Evidence map›Paper›PMID 39160562›Full record

ArticleParasites & vectors2024

Ac-HSP20 regulates autophagy and promotes the encystation of Acanthamoeba castellanii by inhibiting the PI3K/AKT/mTOR signaling pathway.

Siyao Guo, Di Liu, Xi Wan, Dingrui Guo, Meiyu Zheng, Wenyu Zheng, Xianmin Feng

Abstract read
In one paragraph

Article in Parasites & vectors, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Siyao Guo *Department of Pathogenic Biology, Jilin Medical University, Jilin, China.
Di Liu *Department of Pathogenic Biology, Jilin Medical University, Jilin, China.
Xi WanDepartment of Pathogenic Biology, Jilin Medical University, Jilin, China.
Dingrui GuoDepartment of Pathogenic Biology, Jilin Medical University, Jilin, China.
Meiyu ZhengDepartment of Pathogenic Biology, Jilin Medical University, Jilin, China.
Wenyu ZhengDepartment of Microsurgery, Jilin City Central Hospital, Jilin, China. zwy2002468@sina.com.
Xianmin FengDepartment of Pathogenic Biology, Jilin Medical University, Jilin, China. fengxianmin28@163.com.

Funding

National College Students Innovation and Entrepreneurship Training Program X202313706079National Natural Science Foundation of China 32371548
6 · The paper itself

Abstract

backgroundThe encystation of Acanthamoeba castellanii has important ecological and medical significance. Blocking encystation is the key to preventing transmission and curing infections caused by A. castellanii. The formation of autophagosomes is one of the most important changes that occur during the encystation of Acanthamoeba. Our previous studies have shown that the heat shock protein 20 of A. castellanii (Ac-HSP20) is involved in its encystation. This study aimed to determine the role and mechanism of Ac-HSP20 in regulating autophagy involved in the encystation of A. castellanii.

methodsImmunofluorescence assay, western blotting and transmission electron microscopy were used to analyze the dynamic changes in autophagy during the initiation and continuation of encystation. The knockdown of Ac-HSP20 was performed to clarify its regulation of encystation and autophagy and to elucidate the molecular mechanism by which Ac-HSP20 participates in autophagy to promote cyst maturation.

resultsThe encystation rates and autophagosomes were significantly decreased by treatment with the autophagy inhibitor 3-MA. The autophagy marker LC3B and autophagic lysosomes increased with the induced duration of encystation and reached the maximum at 48 h. The encystation rate, LC3B expression and autophagosomes decreased when Ac-HSP20 was knocked down by siRNA transfection. In addition, the expression levels of Ac-HSP20 and LC3B increased and the expressions of p-AKT and p-mTOR decreased after 48 h of encystation without knockdown. However, the expressions of p-AKT and p-mTOR increased while the expression of LC3B decreased under the knockdown of Ac-HSP20. Furthermore, the protein expression of LC3B increased when the PI3K/AKT/mTOR signaling pathway was inhibited but decreased when the pathway was activated.

conclusionsThe results demonstrated that autophagy is positively correlated with the encystation of A. castellanii, and Ac-HSP20 regulates autophagy to maintain the homeostasis of A. castellanii by inhibiting the PI3K /AKT /mTOR signaling pathway, thus promoting the maturation and stability of encystation.

Indexed as

Acanthamoeba castellaniiAutophagyHSP20 Heat-Shock ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionTOR Serine-Threonine KinasesAutophagosomesParasite EncystmentProtozoan ProteinsHSP20 Heat-Shock ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProtozoan ProteinsTOR Serine-Threonine KinasesAcanthamoeba castellaniiAutophagyEncystationHSP20PI3K/AKT/mTORProtozoa

Identifiers

PMID39160562
PMCPMC11331602

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.