![]() Vesicle (EV) production in parasitized red blood cells (pRBCs), an important Infection with Plasmodium falciparum enhances extracellular ![]() Mechanism for parasite-to-parasite communication during the asexual ![]() Therefore, the mechanism of EV production Their organelles through the maturation process, including an important (ESCRT), and in particular the ESCRT-III sub-complex, participates in theįormation of EVs in higher eukaryotes. In the membrane model of giant unilamellar vesicles using the purified Membrane shedding, both reported mechanisms of EV production, were reconstituted Additionally, multivesicular body formation and falciparum-infected RBCs remains to beįalciparum possesses a functional ESCRT-III machineryĪctivated by an alternative recruitment pathway involving the action of PfBro1Īnd PfVps32/PfVps60 proteins. Moreover, the presence of PfVps32, PfVps60 and PfBro1 inĮVs purified from a pRBC culture was confirmed by super-resolution microscopyĪnd dot blot assays. ![]() Increase the knowledge on the underlying molecular mechanisms during malaria Led to a reduction in the number of the produced EVs in the KO strain andĪffected the distribution of other ESCRT-III components. Still a leading cause of death in many low-income countries, and for whichĬurrently available therapeutic strategies are not succeeding in its control, Malaria is a disease caused by Plasmodium parasites that is Pathogenesis and demonstrate that ESCRT-III P.įalciparum proteins participate in EV production. ![]()
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