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重新评估棘阿米巴蛋白酶在组织侵袭中的作用:对 MDCK 细胞单层和仓鼠角膜细胞的细胞病变机制的观察。

Reevaluating the role of Acanthamoeba proteases in tissue invasion: observation of cytopathogenic mechanisms on MDCK cell monolayers and hamster corneal cells.

机构信息

UIICSE Faculty of Superior Studies Iztacala, Medicine, UNAM, Los Reyes Iztacala, 54090 Tlalnepantla, MEX, Mexico.

出版信息

Biomed Res Int. 2013;2013:461329. doi: 10.1155/2013/461329. Epub 2013 Jan 1.

Abstract

The morphological analysis of the cytopathic effect on MDCK cell monolayers and hamster cornea and qualitative and quantitative analyses of conditioned medium and proteases were evaluated and compared between two strains of Acanthamoeba genotype T4. Further than highlighting the biological differences found between both strains, the most important observation in this study was the fact that proteases both in total extracts and in conditioned medium are apparently not determinant in tissue destruction. An interestingly finding was that no lysis of corneal tissue was observed as it was previously suggested. These results, together with previous studies, allow us to conclude that the invasion and disruption of corneal tissue is performed by the penetration of the amoebae through cell junctions, either by the action of proteases promoting cellular separation but not by their destruction and/or a mechanical effect exerted by amoebae. Therefore, contact-dependent mechanisms in Acanthamoeba pathogenesis are more relevant than it has been previously considered. This is supported because the phagocytosis of recently detached cells as well as those attached to the corneal epithelium leads to the modification of the cellular architecture facilitating the migration and destruction of deeper layers of the corneal epithelium.

摘要

对两种棘阿米巴基因型 T4 细胞病变效应在 MDCK 细胞单层和仓鼠角膜上的形态学分析,以及条件培养基和蛋白酶的定性和定量分析进行了评估和比较。本研究的重要观察结果不仅突出了两种菌株之间存在的生物学差异,还表明在总提取物和条件培养基中,蛋白酶显然不是组织破坏的决定因素。一个有趣的发现是,正如之前所建议的那样,没有观察到角膜组织的溶解。这些结果与之前的研究一起,使我们能够得出结论,即阿米巴通过细胞连接的穿透来进行角膜组织的入侵和破坏,这可能是通过蛋白酶促进细胞分离的作用,但不是通过它们的破坏和/或阿米巴施加的机械作用。因此,棘阿米巴病发病机制中的接触依赖性机制比以前认为的更为重要。这是因为最近分离的细胞以及附着在角膜上皮上的细胞的吞噬作用导致细胞结构的改变,从而促进了角膜上皮深层的迁移和破坏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc09/3581277/a89e4e68a4f7/BMRI2013-461329.001.jpg

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