Modulation of Adhesion Molecules Expression by Different Metalloproteases Isolated from <i>Bothrops</i> Snakes

Snake venom metalloproteinases (SVMP) are involved in local inflammatory reactions observed after snakebites. Based on domain composition, they are classified as PI (pro-domain + proteolytic domain), PII (PI + disintegrin-like domains), or PIII (PII + cysteine-rich domains). Here, we studied the rol...

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Autores principales: Bianca C. Zychar, Patrícia B. Clissa, Eneas Carvalho, Adilson S. Alves, Cristiani Baldo, Eliana L. Faquim-Mauro, Luís Roberto C. Gonçalves
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:d50435301b2e4326903e1b6fdff1870f2021-11-25T19:08:57ZModulation of Adhesion Molecules Expression by Different Metalloproteases Isolated from <i>Bothrops</i> Snakes10.3390/toxins131108032072-6651https://doaj.org/article/d50435301b2e4326903e1b6fdff1870f2021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6651/13/11/803https://doaj.org/toc/2072-6651Snake venom metalloproteinases (SVMP) are involved in local inflammatory reactions observed after snakebites. Based on domain composition, they are classified as PI (pro-domain + proteolytic domain), PII (PI + disintegrin-like domains), or PIII (PII + cysteine-rich domains). Here, we studied the role of different SVMPs domains in inducing the expression of adhesion molecules at the microcirculation of the cremaster muscle of mice. We used Jararhagin (Jar)—a PIII SVMP with intense hemorrhagic activity, and Jar-C—a Jar devoid of the catalytic domain, with no hemorrhagic activity, both isolated from <i>B. jararaca</i> venom and BnP-1—a weakly hemorrhagic P1 SVMP from <i>B. neuwiedi</i> venom. Toxins (0.5 µg) or PBS (100 µL) were injected into the scrotum of mice, and 2, 4, or 24 h later, the protein and gene expression of CD54 and CD31 in the endothelium, and integrins (CD11a and CD11b), expressed in leukocytes were evaluated. Toxins induced significant increases in CD54, CD11a, and CD11b at the initial time and a time-related increase in CD31 expression. In conclusion, our results suggest that, despite differences in hemorrhagic activities and domain composition of the SVMPs used in this study, they behave similarly to the induction of expression of adhesion molecules that promote leukocyte recruitment.Bianca C. ZycharPatrícia B. ClissaEneas CarvalhoAdilson S. AlvesCristiani BaldoEliana L. Faquim-MauroLuís Roberto C. GonçalvesMDPI AGarticle<i>Bothrops</i>metalloproteasesinflammationmicrocirculationadhesion moleculesleukocyte-endothelium interactionsMedicineRENToxins, Vol 13, Iss 803, p 803 (2021)
institution DOAJ
collection DOAJ
language EN
topic <i>Bothrops</i>
metalloproteases
inflammation
microcirculation
adhesion molecules
leukocyte-endothelium interactions
Medicine
R
spellingShingle <i>Bothrops</i>
metalloproteases
inflammation
microcirculation
adhesion molecules
leukocyte-endothelium interactions
Medicine
R
Bianca C. Zychar
Patrícia B. Clissa
Eneas Carvalho
Adilson S. Alves
Cristiani Baldo
Eliana L. Faquim-Mauro
Luís Roberto C. Gonçalves
Modulation of Adhesion Molecules Expression by Different Metalloproteases Isolated from <i>Bothrops</i> Snakes
description Snake venom metalloproteinases (SVMP) are involved in local inflammatory reactions observed after snakebites. Based on domain composition, they are classified as PI (pro-domain + proteolytic domain), PII (PI + disintegrin-like domains), or PIII (PII + cysteine-rich domains). Here, we studied the role of different SVMPs domains in inducing the expression of adhesion molecules at the microcirculation of the cremaster muscle of mice. We used Jararhagin (Jar)—a PIII SVMP with intense hemorrhagic activity, and Jar-C—a Jar devoid of the catalytic domain, with no hemorrhagic activity, both isolated from <i>B. jararaca</i> venom and BnP-1—a weakly hemorrhagic P1 SVMP from <i>B. neuwiedi</i> venom. Toxins (0.5 µg) or PBS (100 µL) were injected into the scrotum of mice, and 2, 4, or 24 h later, the protein and gene expression of CD54 and CD31 in the endothelium, and integrins (CD11a and CD11b), expressed in leukocytes were evaluated. Toxins induced significant increases in CD54, CD11a, and CD11b at the initial time and a time-related increase in CD31 expression. In conclusion, our results suggest that, despite differences in hemorrhagic activities and domain composition of the SVMPs used in this study, they behave similarly to the induction of expression of adhesion molecules that promote leukocyte recruitment.
format article
author Bianca C. Zychar
Patrícia B. Clissa
Eneas Carvalho
Adilson S. Alves
Cristiani Baldo
Eliana L. Faquim-Mauro
Luís Roberto C. Gonçalves
author_facet Bianca C. Zychar
Patrícia B. Clissa
Eneas Carvalho
Adilson S. Alves
Cristiani Baldo
Eliana L. Faquim-Mauro
Luís Roberto C. Gonçalves
author_sort Bianca C. Zychar
title Modulation of Adhesion Molecules Expression by Different Metalloproteases Isolated from <i>Bothrops</i> Snakes
title_short Modulation of Adhesion Molecules Expression by Different Metalloproteases Isolated from <i>Bothrops</i> Snakes
title_full Modulation of Adhesion Molecules Expression by Different Metalloproteases Isolated from <i>Bothrops</i> Snakes
title_fullStr Modulation of Adhesion Molecules Expression by Different Metalloproteases Isolated from <i>Bothrops</i> Snakes
title_full_unstemmed Modulation of Adhesion Molecules Expression by Different Metalloproteases Isolated from <i>Bothrops</i> Snakes
title_sort modulation of adhesion molecules expression by different metalloproteases isolated from <i>bothrops</i> snakes
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/d50435301b2e4326903e1b6fdff1870f
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