Cytotoxic effects of crotamine are mediated through lysosomal membrane permeabilization


Autoria(s): HAYASHI, Mirian A. F.; NASCIMENTO, Fabio D.; KERKIS, Alexandre; OLIVEIRA, Vitor; OLIVEIRA, Eduardo B.; PEREIRA, Alexandre; RADIS-BAPTISTA, Gandhi; NADER, Helena B.; YAMANE, Tetsuo; KERKIS, Irina; TERSARIOL, Ivarne L. S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

Crotamine, one of the main toxic components of Crotalus durissus terrificus venom, is a small non-enzymatic basic polypeptide, which causes hind limb paralysis and necrosis of muscle cells. it is well-known that several toxins penetrate into the cytosol through endocytosis, although in many cases the mechanism by which this occurs has not been fully investigated. Recently, using low concentrations of crotamine, we demonstrated the uptake of this toxin into actively proliferative cells via endocytosis, an event that ensues crotamine binding to cell membrane heparan sulfate proteoglycans. Thus, crotamine can be regarded as a cell-penetrating peptide that, additionally, has been shown to be able of delivering some biologically active molecules into various cells. Herein, we investigate one of the mechanisms by which crotamine exerts its cytotoxic effects by following its uptake into highly proliferative cells, as CHO-K1 cells. Crotamine accumulation in the acidic endosomal/lysosomal vesicles was observed within 5 min after treatment of these cells with a cytotoxic concentration of this toxin, a value determined here by classical MTT assay. This accumulation caused disruption of lysosomal vesicles accompanied by the leakage of these vesicles contents into the cytosol. This lysosomal lysis also promoted the release of cysteine cathepsin and an increase of caspase activity in the cytoplasm. This chain of events seems to trigger a cell death process. Overall, our data suggest that lysosomes are the primary targets for crotamine cytotoxicity, a proposal corroborated by the correlation between both the kinetics and concentration-dependence of crotamine accumulation in lysosome compartments and the cytotoxic effects of this protein in CHO-K1 cells. Although crotamine is usually regarded as a myotoxin, we observed that intraperitoneal injection of fluorescently labeled crotamine in living mice led to significant and rapid accumulation of this toxin in the cell cytoplasm of several tissues, suggesting that crotamine cytotoxicity might not be restricted to muscle cells. (C) 2008 Elsevier Ltd. All rights reserved.

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Identificador

TOXICON, v.52, n.3, p.508-517, 2008

0041-0101

http://producao.usp.br/handle/BDPI/23789

10.1016/j.toxicon.2008.06.029

http://dx.doi.org/10.1016/j.toxicon.2008.06.029

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Toxicon

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #Toxin #Crotamine #Lysosome #Cellular uptake #Cell-penetrating peptides #Highly proliferative cells #Protease #Cytotoxicity #CELL-PENETRATING PEPTIDES #CROTALUS-DURISSUS-TERRIFICUS #ACRIDINE-ORANGE #INDUCED APOPTOSIS #CYSTEINE CATHEPSINS #MAMMALIAN-CELL #CHOLERA-TOXIN #DEATH #ACTIVATION #DELIVERY #Pharmacology & Pharmacy #Toxicology
Tipo

article

original article

publishedVersion