Literature DB >> 18662711

Cytotoxic effects of crotamine are mediated through lysosomal membrane permeabilization.

Mirian A F Hayashi1, Fábio D Nascimento, Alexandre Kerkis, Vitor Oliveira, Eduardo B Oliveira, Alexandre Pereira, Gandhi Rádis-Baptista, Helena B Nader, Tetsuo Yamane, Irina Kerkis, Ivarne L S Tersariol.   

Abstract

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 in 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.

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Year:  2008        PMID: 18662711     DOI: 10.1016/j.toxicon.2008.06.029

Source DB:  PubMed          Journal:  Toxicon        ISSN: 0041-0101            Impact factor:   3.033


  21 in total

Review 1.  Privileged frameworks from snake venom.

Authors:  T A Reeks; B G Fry; P F Alewood
Journal:  Cell Mol Life Sci       Date:  2015-02-19       Impact factor: 9.261

2.  Role of the inflammasome in defense against venoms.

Authors:  Noah W Palm; Ruslan Medzhitov
Journal:  Proc Natl Acad Sci U S A       Date:  2013-01-07       Impact factor: 11.205

Review 3.  The endolysosomal system in cell death and survival.

Authors:  Urška Repnik; Maruša Hafner Česen; Boris Turk
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-01-01       Impact factor: 10.005

Review 4.  Toxin bioportides: exploring toxin biological activity and multifunctionality.

Authors:  Irina Kerkis; Alvaro Rossan de Brandão Prieto da Silva; Celine Pompeia; Jan Tytgat; Paulo L de Sá Junior
Journal:  Cell Mol Life Sci       Date:  2016-08-23       Impact factor: 9.261

5.  Crotamine, a cell-penetrating peptide, is able to translocate parthenogenetic and in vitro fertilized bovine embryos but does not improve exogenous DNA expression.

Authors:  Iana S Campelo; Natalia G Canel; Romina J Bevacqua; Luciana M Melo; Gandhi Rádis-Baptista; Vicente J F Freitas; Daniel F Salamone
Journal:  J Assist Reprod Genet       Date:  2016-08-11       Impact factor: 3.412

6.  DNA-interactive properties of crotamine, a cell-penetrating polypeptide and a potential drug carrier.

Authors:  Pei-Chun Chen; Mirian A F Hayashi; Eduardo Brandt Oliveira; Richard L Karpel
Journal:  PLoS One       Date:  2012-11-08       Impact factor: 3.240

7.  Anticancer Activity of Cobra Venom Polypeptide, Cytotoxin-II, against Human Breast Adenocarcinoma Cell Line (MCF-7) via the Induction of Apoptosis.

Authors:  Karim Ebrahim; Farshad H Shirazi; Hosein Vatanpour; Abas Zare; Farzad Kobarfard; Hadi Rabiei
Journal:  J Breast Cancer       Date:  2014-12-26       Impact factor: 3.588

8.  Crotamine induces browning of adipose tissue and increases energy expenditure in mice.

Authors:  Marcelo P Marinovic; Joana D Campeiro; Sunamita C Lima; Andrea L Rocha; Marcela B Nering; Eduardo B Oliveira; Marcelo A Mori; Mirian A F Hayashi
Journal:  Sci Rep       Date:  2018-03-22       Impact factor: 4.379

9.  Anthrax lethal toxin induced lysosomal membrane permeabilization and cytosolic cathepsin release is Nlrp1b/Nalp1b-dependent.

Authors:  Kathleen M Averette; Matthew R Pratt; Yanan Yang; Sara Bassilian; Julian P Whitelegge; Joseph A Loo; Tom W Muir; Kenneth A Bradley
Journal:  PLoS One       Date:  2009-11-18       Impact factor: 3.240

Review 10.  State of the art in the studies on crotamine, a cell penetrating peptide from South American rattlesnake.

Authors:  Irina Kerkis; Mirian A F Hayashi; Alvaro R B Prieto da Silva; Alexandre Pereira; Paulo Luiz De Sá Júnior; Andre J Zaharenko; Gandhi Rádis-Baptista; Alexandre Kerkis; Tetsuo Yamane
Journal:  Biomed Res Int       Date:  2014-01-15       Impact factor: 3.411

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