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p38丝裂原活化蛋白激酶(MAPK)抑制剂SB203580可抑制犬新孢子虫的细胞侵袭。

The p38 MAPK inhibitor, SB203580, inhibits cell invasion by Neospora caninum.

作者信息

Jin Xiaoxia, Gong Pengtao, Li Guojiang, Zhang Xichen, Li Jianhua

机构信息

Key Laboratory of Zoonosis, Ministry of Education, College of Veterinary Medicine, Jilin University, 5333 Xian Road, Changchun, 130062, China.

Jilin Agricultural Science and Technology University, 77 Hanlin Road, Jilin, 132101, China.

出版信息

Parasitol Res. 2017 Feb;116(2):813-819. doi: 10.1007/s00436-016-5346-1. Epub 2016 Dec 30.

DOI:10.1007/s00436-016-5346-1
PMID:28039498
Abstract

The Apicomplexan parasite Neospora caninum is an obligate intracellular parasitic protozoan. It can cause severe diseases in a number of animals throughout the world. Infection with N. caninum leads to abortions in pregnant animals and neuromuscular disorders of newborns which cause great economic losses to animal husbandry. However, the mechanism of cell invasion by N. caninum is still unclear. This paper aims to investigate the impact of SB203580, a p38 MAPK inhibitor, on host cell invasion by N. caninum. The results suggested the presence of putative p38 MAPK homologues in N. caninum, and incubation of N. caninum with SB203580 markedly reduced the tachyzoite motility and microneme exocytosis (NcMIC2, 3, and 6). Furthermore, treatment or pretreatment of MDBK cells with SB203580 effectively reduced cell invasion by N. caninum. Therefore, SB203580 affected both, parasites and host cells, resulting in inhibition of cell invasion by N. caninum.

摘要

顶复门寄生虫犬新孢子虫是一种专性细胞内寄生原生动物。它可在世界各地的多种动物中引发严重疾病。犬新孢子虫感染会导致怀孕动物流产以及新生动物出现神经肌肉紊乱,给畜牧业造成巨大经济损失。然而,犬新孢子虫入侵细胞的机制仍不清楚。本文旨在研究p38丝裂原活化蛋白激酶(MAPK)抑制剂SB203580对犬新孢子虫入侵宿主细胞的影响。结果表明犬新孢子虫中存在假定的p38 MAPK同源物,用SB203580孵育犬新孢子虫可显著降低速殖子的运动性和微线体胞吐作用(NcMIC2、3和6)。此外,用SB203580处理或预处理MDBK细胞可有效降低犬新孢子虫对细胞的入侵。因此,SB203580对寄生虫和宿主细胞均有影响,从而抑制了犬新孢子虫对细胞的入侵。

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本文引用的文献

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MIC3, a novel cross-protective antigen expressed in Toxoplasma gondii and Neospora caninum.MIC3,一种在刚地弓形虫和犬新孢子虫中表达的新型交叉保护性抗原。
Parasitol Res. 2015 Oct;114(10):3791-9. doi: 10.1007/s00436-015-4609-6. Epub 2015 Jul 5.
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Identification and characterization of a microneme protein (NcMIC6) in Neospora caninum.犬新孢子虫中一种微小膜泡蛋白(NcMIC6)的鉴定与特性分析
Parasitol Res. 2015 Aug;114(8):2893-902. doi: 10.1007/s00436-015-4490-3. Epub 2015 May 10.
3
Reduced parasite motility and micronemal protein secretion by a p38 MAPK inhibitor leads to a severe impairment of cell invasion by the apicomplexan parasite Eimeria tenella.
RNA sequencing reveals dynamic expression of lncRNAs and mRNAs in caprine endometrial epithelial cells induced by Neospora caninum infection.
RNA 测序揭示了弓形虫感染诱导的山羊子宫内膜上皮细胞中长非编码 RNA 和信使 RNA 的动态表达。
Parasit Vectors. 2022 Aug 24;15(1):297. doi: 10.1186/s13071-022-05405-5.
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p38MAPK Signaling Pathway in Osteoarthritis: Pathological and Therapeutic Aspects.骨关节炎中的p38丝裂原活化蛋白激酶信号通路:病理及治疗方面
J Inflamm Res. 2022 Feb 3;15:723-734. doi: 10.2147/JIR.S348491. eCollection 2022.
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Activation of a EGFR-Like Kinase Facilitates Intracellular Parasite Proliferation.一种类表皮生长因子受体激酶的激活促进细胞内寄生虫增殖。
Front Microbiol. 2017 Oct 12;8:1980. doi: 10.3389/fmicb.2017.01980. eCollection 2017.
p38丝裂原活化蛋白激酶抑制剂降低寄生虫活力和微线体蛋白分泌,导致顶复门寄生虫柔嫩艾美耳球虫的细胞侵袭严重受损。
PLoS One. 2015 Feb 17;10(2):e0116509. doi: 10.1371/journal.pone.0116509. eCollection 2015.
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