1986
DOI: 10.1016/0014-4894(86)90049-4
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Tritrichomonas foetus: Ultrastructure and cytochemistry of endocytosis

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Cited by 17 publications
(7 citation statements)
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“…We previously observed that the alteration of parasite morphology due to iron depletion was followed by a significantly different expression of cytoskeleton-related proteins and proteins involved in cell signalling (de Jesus et al 2007 ). The cell surface of trichomonads exhibits an active endocytic machinery ( Benchimol et al 1986, 19 , 1990 ) and it has been suggested that during pseudocyst formation, the flagella are internalised by a receptor-mediated endocytosis process ( Granger et al 2000 , Pereira-Neves et al 2003 ). In addition, we observed that the sequence of flagellar internalisation was similar to that observed in T. foetus , where the recurrent flagellum is internalised first, followed by the anterior flagella ( Pereira-Neves et al 2003 ).…”
Section: Discussionmentioning
confidence: 99%
“…We previously observed that the alteration of parasite morphology due to iron depletion was followed by a significantly different expression of cytoskeleton-related proteins and proteins involved in cell signalling (de Jesus et al 2007 ). The cell surface of trichomonads exhibits an active endocytic machinery ( Benchimol et al 1986, 19 , 1990 ) and it has been suggested that during pseudocyst formation, the flagella are internalised by a receptor-mediated endocytosis process ( Granger et al 2000 , Pereira-Neves et al 2003 ). In addition, we observed that the sequence of flagellar internalisation was similar to that observed in T. foetus , where the recurrent flagellum is internalised first, followed by the anterior flagella ( Pereira-Neves et al 2003 ).…”
Section: Discussionmentioning
confidence: 99%
“…This could be explained by the size of mammalian cells, which is many times larger than the parasite, since previous studies have shown that living or dead yeast (Pereira-Neves and Benchimol, 2007) and bacteria (Benchimol and De Souza, 1995; Francioli et al 1983) are promptly ingested by trichomonads. Other cell surface elements might also be involved in cell recognition since some bacterial strains are not ingested by T. vaginalis (Pereira-Neves and Benchimol, unpublished observations) whereas in other cell types, fibronectin, carbohydrates and other cell surface molecules are important factors (Benchimol et al 1986, 1990, 2008; Bonilha et al 1995). Thus, T. vaginalis seems to act differently from amoebae, which are able to ingest epithelial cells regardless of whether they have been previously lysed or not (Martinez-Palomo et al 1985).…”
Section: Discussionmentioning
confidence: 99%
“…The size of internalized particles or structures does not necessarily determine which mechanism predominates, although in mammalian macrophages the contribution of phagocytosis generally increases with increasing particle size (Pratten and Lloyd 1986;Koval et al 1998). A very active endocytic machinery exists at the T. foetus cell surface (Benchimol et al 1981(Benchimol et al , 1986(Benchimol et al , 1990(Benchimol et al , 1992Queiroz et al 1991;Aonso et al 1994Aonso et al , 1997Granger and Warwood 1996;Tachezy et al 1996Tachezy et al , 1998, raising the possibility that the¯agella might be laterally internalized by a process akin to receptor-mediated endocytosis. Hypertonic medium inhibits clathrin-mediated endocytosis in mammalian cells by preventing clathrin from interacting with adaptor proteins (Daukas and Zigmond 1985;Hansen et al 1993); these conditions also inhibited¯a-gellar internalization by T. foetus.…”
Section: Discussionmentioning
confidence: 99%