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成纤维细胞生长因子受体 A 协调血吸虫生物学和宿主-寄生虫相互作用中的多种功能。

Fibroblast Growth Factor Receptor A Orchestrates Multiple Functions in Schistosome Biology and in the Host-Parasite Interplay.

机构信息

Infection and Inflammation Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.

出版信息

Front Immunol. 2022 Jun 22;13:868077. doi: 10.3389/fimmu.2022.868077. eCollection 2022.

DOI:10.3389/fimmu.2022.868077
PMID:35812433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9257043/
Abstract

Stem cells play significant roles in driving the complex life cycle of . Fibroblast growth factor (FGF) receptor A (SmFGFRA) is essential for maintaining the integrity of schistosome stem cells. Using immunolocalization, we demonstrated that SmFGFRA was distributed abundantly in germinal/stem cells of different life stages including eggs, miracidia, cercariae, schistosomula and adult worms. Indeed, SmFGFRA was also localized amply in embryonic cells and in the perinuclear region of immature eggs; von Lichtenberg's layer and the neural mass of mature eggs; the ciliated surface and neural mass of miracidia; the tegument cytosol of cercariae, schistosomula and adult worms; and was present in abundance in the testis and vitellaria of adult worms of . The distribution pattern of SmFGFRA illustrates the importance of this molecule in maintaining stem cells, development of the nervous and reproductive system of schistosomes, and in the host-parasite interplay. We showed SmFGFRA can bind human FGFs, activating the mitogen activated protein kinase (MAPK) pathway of adult worms . Inhibition of FGF signaling by the specific tyrosine kinase inhibitor BIBF 1120 significantly reduced egg hatching ability and affected the behavior of miracidia hatched from the treated eggs, emphasizing the importance of FGF signaling in driving the life cycle of . Our findings provide increased understanding of the complex schistosome life cycle and host-parasite interactions, indicating components of the FGF signaling pathway may represent promising targets for developing new interventions against schistosomiasis.

摘要

干细胞在驱动 的复杂生命周期中起着重要作用。成纤维细胞生长因子 (FGF) 受体 A (SmFGFRA) 对于维持血吸虫干细胞的完整性至关重要。通过免疫定位,我们证明 SmFGFRA 在不同生命周期阶段的生殖/干细胞中大量分布,包括卵、毛蚴、尾蚴、童虫和成虫。事实上,SmFGFRA 也在胚胎细胞和未成熟卵的核周区、von Lichtenberg 层和成熟卵的神经团、纤毛表面和神经团、尾蚴、童虫和成虫的体被质中大量存在,并在成虫的睾丸和卵黄腺中大量存在。SmFGFRA 的分布模式表明该分子在维持干细胞、血吸虫神经系统和生殖系统的发育以及宿主-寄生虫相互作用方面的重要性。我们表明 SmFGFRA 可以结合人 FGFs,激活成虫的丝裂原激活蛋白激酶 (MAPK) 途径。特异性酪氨酸激酶抑制剂 BIBF 1120 抑制 FGF 信号显著降低了卵的孵化能力,并影响了从处理过的卵中孵化的毛蚴的行为,强调了 FGF 信号在驱动 的生命周期中的重要性。我们的发现增加了对复杂血吸虫生命周期和宿主-寄生虫相互作用的理解,表明 FGF 信号通路的成分可能代表开发针对血吸虫病的新干预措施的有前途的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/ae05ca154097/fimmu-13-868077-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/727f7acfeaae/fimmu-13-868077-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/fc984536d117/fimmu-13-868077-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/df246b022dc8/fimmu-13-868077-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/c94fa6d7f2fc/fimmu-13-868077-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/dce75e39ea85/fimmu-13-868077-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/fbecb6e2af7e/fimmu-13-868077-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/ae05ca154097/fimmu-13-868077-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/727f7acfeaae/fimmu-13-868077-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/fc984536d117/fimmu-13-868077-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/c3607c8314d3/fimmu-13-868077-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/a4f11a488ebb/fimmu-13-868077-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/df246b022dc8/fimmu-13-868077-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/c94fa6d7f2fc/fimmu-13-868077-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/dce75e39ea85/fimmu-13-868077-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/fbecb6e2af7e/fimmu-13-868077-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de93/9257043/ae05ca154097/fimmu-13-868077-g009.jpg

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