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J. Venom. Anim. Toxins incl. Trop. Dis.

V.19, p.213-220, 2013.

Original paper - ISSN 1678-9199.

 

Cathepsin B/X is secreted by Echinometra lucunter sea urchin spines, a structure rich in granular cells and toxins

 
Juliana Mozer Sciani 1 2 , Marta Maria Antoniazzi 3 , Adriana da Costa Neves 3 , Daniel Carvalho Pimenta 1 2 *

1Laboratory of Biochemistry and Biophysics, Butantan Institute, São Paulo, São Paulo, Brazil

2Center of Marine Biology, University of São Paulo, São Sebastião, São Paulo, Brazil

3Laboratory of Cell Biology, Butantan Institute, São Paulo, São Paulo State, Brazil

ABSTRACT

 

Background

Echinometra lucunter is a common American sea urchin responsible for the majority of the marine accidents in Brazil. Although not lethal, these accidents are reported to be extremely painful. Recently, our group described the presence of toxins in its spines that contribute to the pathological reactions. Additionally, we have observed that the E. lucunter spines can regenerate when broken. In the present work we evaluated the enzymatic activities of sea urchin spine extracts in order to identify an enzyme that could contribute not only to the toxicity, but also participate in the spine growth and regeneration.

 

Results

The spine aqueous extract was tested for peptidase activity, with synthetic substrates, in the presence and absence of inhibitors and activators. For proper enzyme classification, the FRET-substrate cleavage pattern, pH-dependency activity and Western-blot analyses were performed. The spine extract was able to cleave Z-R-MCA and Abz-GIVRAK(Dnp)-OH following pre-incubation with DTT, and was inhibited by E-64. Furthermore, the double-peaked pH curve (5 and 7) and the cleavage site proportion (4:6, R|A:A|K) indicate the presence of both mono and dicarboxypeptidase activities. Moreover, in Western-blot analysis, the spine extract was positive for anti-cathepsin B antibody.

 

Conclusions

E. lucunter spines extracts presented a cysteine peptidase activity that was identified as cathepsin B/X that would participate in the remodeling and growth processes of the spine, as well as in the inflammatory response to the accident.

 

Key words: Echinometra lucunter; Spines; Cathepsin; Proteolysis

 

Received: July 29, 2013; Revised: December 9, 2013; Accepted: December 16, 2013

 

Correspondence: dcpimenta@butantan.gov.br

 

Authors' contributions

JMS, Ph.D. student from the University of São Paulo, collected the sea urchins and carried out experiments of purification, Western blotting and kinetic assays; MMA and ACM performed the histology and immunohistochemistry experiments. DCP designed the work and supervised the conduction of most experiments. All authors contributed to the final manuscript. All authors read and approved the final manuscript.

 

Competing interests

The authors declare that there are no competing interests.