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Distribution of Clathrin During Electron Dense Granule Secretion of Entamoeba histolytica Trophozoites

机译:ElecoEBA组织晶晶体致密颗粒分泌术期间Clathrin分布

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In vitro interaction of Entamoeba histolytica with collagen type I and Ca~(2+) induces intracellular formation and release of electron-dense granules (EDG) and stimulation of collagenolytic activity. Because EDG contain collagenase activity, we have postulated that EDG participates in tissue destruction during invasive amebiasis. Clathrin mediates cargo selection and vesicle fusion at the TGN, in the endosomal, lysosomal, and regulated secretory pathways as well as endo-cytosis at the plasma membrane of eukaryote cells. More recently it has been also demonstrated that reassembly of the Golgi apparatus required the presence of clathrin heavy chain. Because the role of clathrin in EDG secretion is unknown the main aim of our study is to determine the role of this protein in EDG formation and release. Electron and confocal microscopy using specific antibodies showed that clathrin participates in E. histolytica EDG secretion. E. histolytica is a human pathogen that has the potential to destroy any host tissue. Previously, we demonstrated an increased expression and secretion of EDG containing collagenase activity when trophozoites interact with collagen type I and Ca~(2+) (1). This induction is achieved through an increase of adhesion, tyrosine phosphorylation and activation of pp125~(FAK) and p42~(MAPK), which results in cytoskeleton organization (2).
机译:在溶组织内阿米巴与胶原类型体外相互作用我和Ca〜(2+)诱导的细胞内形成和电子致密颗粒(EDG)和溶胶原活性的刺激的释放。因为EDG含有胶原酶活性,我们推测,EDG侵入阿米巴病过程中的组织破坏参与。网格蛋白介导的货物选择和囊泡融合在TGN,在核内体,溶酶体,和调节的分泌途径以及内切cytosis在真核细胞的质膜。最近它已被还证实了重组高尔基体所需要的网格蛋白重链的存在。由于网格蛋白的分泌EDG的作用是未知的我们研究的主要目的是确定EDG形成和释放这种蛋白质的作用。电子和使用特异性抗体共聚焦显微镜显示,溶组织内阿米巴EDG分泌是网格蛋白参与。溶组织内阿米巴是具有摧毁任何宿主组织的潜在人类病原体。先前,我们证明含有胶原酶活性EDG的增加的表达和分泌时滋养体相互作用与I型胶原蛋白和Ca〜(2+)(1)。这种诱导是通过增加附着力,酪氨酸磷酸化和pp125〜(FAK)和p42〜(MAPK)的活化,其导致细胞骨架的组织(2)来实现的。

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