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Published on: March 16, 2018
Macrophage damage by Leishmania amazonensis cytolysin: evidence of pore formation on cell membrane
F S Noronha1, J S Cruz, P S Beirão
1Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais 31270-010, Brazil.
Abstract:
We have previously shown that both promastigotes and amastigotes of Leishmania amazonensis contain a lytic protein that damages erythrocytes and nucleated cells, including macrophages (F. S. M. Noronha, F. J. Ramalho-Pinto, and M. F. Horta, Infect. Immun. 64:3975-3982, 1996). Using the patch-clamp technique, we show here that cell damage by parasite extracts is mediated by the formation of nonselective pores on the target membrane. This demonstrates that L. amazonensis cytolysin is a pore-forming protein (PFP), here named leishporin. We show that the diameters of the pores formed by parasite extracts are heterogeneous, varying from approximately 1.6 to >6.1 nm according to cytolysin concentration or time. We also show that pore formation involves the binding of the PFP to the target cell membrane, a temperature-independent event that is necessary but not sufficient to lyse cells. This is followed by a temperature-dependent step that triggers lysis, probably the insertion and the polymerization of protein subunits in the lipid bilayer. We provide evidence that suggests that polymerization of single subunits must occur for pore formation. We show, in addition, that L. amazonensis expresses molecules antigenically homologous to other PFPs.
Insights
Leishmania amazonensis releases a cytolysin, leishporin, that forms pores in cell membranes, causing cell damage. This pore-forming protein (PFP) requires polymerization for lysis, with pore size varying by concentration.
Area of Science:
- Parasitology
- Cell Biology
- Biochemistry
Background:
- Leishmania amazonensis, a parasite, possesses a lytic protein affecting host cells.
- Previous studies indicated damage to erythrocytes and nucleated cells, including macrophages.
Purpose of the Study:
- To investigate the mechanism of cell damage induced by Leishmania amazonensis.
- To characterize the lytic protein as a pore-forming protein (PFP).
Main Methods:
- Patch-clamp technique to analyze membrane electrical properties.
- Utilized parasite extracts to study pore formation.
- Investigated temperature-dependent and independent steps in lysis.
Main Results:
- Leishmania amazonensis cytolysin forms nonselective pores (1.6 to >6.1 nm) in target membranes.
- Pore formation involves temperature-independent binding and temperature-dependent polymerization of protein subunits.
- Evidence suggests subunit polymerization is essential for pore formation.
- Homologous molecules to other PFPs are expressed by L. amazonensis.
Conclusions:
- Leishmania amazonensis cytolysin, termed leishporin, is a pore-forming protein (PFP).
- Leishporin mediates cell damage through pore formation, requiring subunit polymerization for lysis.
- The parasite expresses molecules antigenically similar to other known PFPs.
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