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10.1038/s41374-020-0420-9

http://scihub22266oqcxt.onion/10.1038/s41374-020-0420-9
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32238906!7111589!32238906
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suck abstract from ncbi


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pmid32238906      Lab+Invest 2020 ; 100 (8): 1030-1041
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  • Increased talin-vinculin spatial proximities in livers in response to spotted fever group rickettsial and Ebola virus infections #MMPMID32238906
  • Liu Y; Xiao J; Zhang B; Shelite TR; Su Z; Chang Q; Judy B; Li X; Drelich A; Bei J; Zhou Y; Zheng J; Jin Y; Rossi SL; Tang SJ; Wakamiya M; Saito T; Ksiazek T; Kaphalia B; Gong B
  • Lab Invest 2020[Aug]; 100 (8): 1030-1041 PMID32238906show ga
  • Talin and vinculin, both actin-cytoskeleton-related proteins, have been documented to participate in establishing bacterial infections, respectively, as the adapter protein to mediate cytoskeleton-driven dynamics of the plasma membrane. However, little is known regarding the potential role of the talin-vinculin complex during spotted fever group rickettsial and Ebola virus infections, two dreadful infectious diseases in humans. Many functional properties of proteins are determined by their participation in protein-protein complexes, in a temporal and/or spatial manner. To resolve the limitation of application in using mouse primary antibodies on archival, multiple formalin-fixed mouse tissue samples, which were collected from experiments requiring high biocontainment, we developed a practical strategic proximity ligation assay (PLA) capable of employing one primary antibody raised in mouse to probe talin-vinculin spatial proximal complex in mouse tissue. We observed an increase of talin-vinculin spatial proximities in the livers of spotted fever Rickettsia australis or Ebola virus-infected mice when compared with mock mice. Furthermore, using EPAC1-knockout mice, we found that deletion of EPAC1 could suppress the formation of spatial proximal complex of talin-vinculin in rickettsial infections. In addition, we observed increased colocalization between spatial proximity of talin-vinculin and filamentous actin-specific phalloidin staining in single survival mouse from an ordinarily lethal dose of rickettsial or Ebola virus infection. These findings may help to delineate a fresh insight into the mechanisms underlying liver specific pathogenesis during infection with spotted fever rickettsia or Ebola virus in the mouse model.
  • |Actin Cytoskeleton/*metabolism[MESH]
  • |Animals[MESH]
  • |Cell Membrane/*metabolism[MESH]
  • |Cells, Cultured[MESH]
  • |Guanine Nucleotide Exchange Factors/genetics/metabolism[MESH]
  • |Hemorrhagic Fever, Ebola/*metabolism[MESH]
  • |Humans[MESH]
  • |Liver/*metabolism/microbiology/virology[MESH]
  • |Mice, Knockout[MESH]
  • |Protein Binding[MESH]
  • |Rickettsia/physiology[MESH]
  • |Spotted Fever Group Rickettsiosis/metabolism/microbiology[MESH]
  • |Talin/chemistry/*metabolism[MESH]


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