Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/34889
Title: Intracellular proteolysis of kininogen by malaria parasites promotes release of active kinins
Authors: Bagnaresi, Piero [UNIFESP]
Barros, Nilana Meza Tenório [UNIFESP]
Assis, Diego M. [UNIFESP]
Melo, Pollyana M. S. [UNIFESP]
Fonseca, Raphael G. [UNIFESP]
Juliano, Maria Aparecida [UNIFESP]
Pesquero, João Bosco [UNIFESP]
Juliano, Luiz [UNIFESP]
Rosenthal, Philip J.
Carmona, Adriana Karaoglanovic [UNIFESP]
Gazarini, Marcos Leoni [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Univ Calif San Francisco
Issue Date: 7-May-2012
Publisher: Biomed Central Ltd
Citation: Malaria Journal. London: Biomed Central Ltd, v. 11, 10 p., 2012.
Abstract: Background: the malaria burden remains a major public health concern, especially in sub-Saharan Africa. the complex biology of Plasmodium, the apicomplexan parasite responsible for this disease, challenges efforts to develop new strategies to control the disease. Proteolysis is a fundamental process in the metabolism of malaria parasites, but roles for proteases in generating vasoactive peptides have not previously been explored.Results: in the present work, it was demonstrated by mass spectrometry analysis that Plasmodium parasites (Plasmodium chabaudi and Plasmodium falciparum) internalize and process plasma kininogen, thereby releasing vasoactive kinins (Lys-BK, BK and des-Arg(9)-BK) that may mediate haemodynamic alterations during acute malaria. in addition, it was demonstrated that the P. falciparum cysteine proteases falcipain-2 and falcipain-3 generated kinins after incubation with human kininogen, suggesting that these enzymes have an important role in this process. the biologic activity of peptides released by Plasmodium parasites was observed by measuring ileum contraction and activation of kinin receptors (B1 and B2) in HUVEC cells; the peptides elicited an increase in intracellular calcium, measured by Fluo-3 AM fluorescence. This effect was suppressed by the specific receptor antagonists Des-Arg(9)[Leu(8)]-BK and HOE-140.Conclusions: in previously undescribed means of modulating host physiology, it was demonstrated that malaria parasites can generate active kinins by proteolysis of plasma kininogen.
URI: http://repositorio.unifesp.br/handle/11600/34889
ISSN: 1475-2875
Other Identifiers: http://dx.doi.org/10.1186/1475-2875-11-156
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