Strong renal expression of heat shock protein 70, high mobility group box 1, inducible nitric oxide synthase, and nitrotyrosine in mice model of severe malaria
Abstract INTRODUCTION Renal damage is a consequence of severe malaria, and is generally caused by sequestration of Plasmodium falciparum -infected erythrocytes in the renal microcirculation, which leads to obstruction, hypoxia, and ischemia. This triggers high mobility group box 1 (HMGB1) to send a...
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Sociedade Brasileira de Medicina Tropical (SBMT)
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Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822017000400489&lng=en&tlng=en |
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author | Loeki Enggar Fitri Ervina Rosmarwati Yesita Rizky Niniek Budiarti Nur Samsu Karyono Mintaroem |
author_facet | Loeki Enggar Fitri Ervina Rosmarwati Yesita Rizky Niniek Budiarti Nur Samsu Karyono Mintaroem |
author_sort | Loeki Enggar Fitri |
collection | DOAJ |
description | Abstract INTRODUCTION Renal damage is a consequence of severe malaria, and is generally caused by sequestration of Plasmodium falciparum -infected erythrocytes in the renal microcirculation, which leads to obstruction, hypoxia, and ischemia. This triggers high mobility group box 1 (HMGB1) to send a danger signal through toll-like receptors 2 and 4. This signal up-regulates inducible nitric oxide (iNOS) and nitrotyrosine to re-perfuse the tissue, and also increases heat shock protein 70 (HSP70) expression. As no study has examined the involvement of intracellular secondary molecules in this setting, the present study compared the renal expressions of HSP70, HMGB1, iNOS, and nitrotyrosine between mice suffered from severe malaria and normal mice. METHODS C57BL/6 mice were divided into an infected group (intraperitoneal injection of 10 6 P. berghei ANKA) and a non-infected group. Renal damage was evaluated using hematoxylin eosin staining, and immunohistochemistry was used to evaluate the expressions of HSP70, HMGB1, iNOS, and nitrotyrosine. RESULTS Significant inter-group differences were observed in the renal expressions of HSP70, HMGB1, and iNOS (p=0.000, Mann-Whitney test), as well as nitrotyrosine (p=0.000, independent t test). The expressions of HSP70 and HMGB1 were strongly correlated (p=0.000, R=1.000). No correlations were observed between iNOS and HMGB, HMGB1 and nitrotyrosine, HSP70 and nitrotyrosine, or iNOS and nitrotyrosine. CONCLUSIONS It appears that HMGB1, HSP70, iNOS, and nitrotyrosine play roles in the renal damage that is observed in mice with severe malaria. Only HSP70 expression is strongly correlated with the expression of HMGB1. |
first_indexed | 2024-04-12T14:45:28Z |
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issn | 1678-9849 |
language | English |
last_indexed | 2024-04-12T14:45:28Z |
publisher | Sociedade Brasileira de Medicina Tropical (SBMT) |
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series | Revista da Sociedade Brasileira de Medicina Tropical |
spelling | doaj.art-97dccce714324a68ac36901ec1f9167b2022-12-22T03:28:39ZengSociedade Brasileira de Medicina Tropical (SBMT)Revista da Sociedade Brasileira de Medicina Tropical1678-984950448949810.1590/0037-8682-0049-2017S0037-86822017000400489Strong renal expression of heat shock protein 70, high mobility group box 1, inducible nitric oxide synthase, and nitrotyrosine in mice model of severe malariaLoeki Enggar FitriErvina RosmarwatiYesita RizkyNiniek BudiartiNur SamsuKaryono MintaroemAbstract INTRODUCTION Renal damage is a consequence of severe malaria, and is generally caused by sequestration of Plasmodium falciparum -infected erythrocytes in the renal microcirculation, which leads to obstruction, hypoxia, and ischemia. This triggers high mobility group box 1 (HMGB1) to send a danger signal through toll-like receptors 2 and 4. This signal up-regulates inducible nitric oxide (iNOS) and nitrotyrosine to re-perfuse the tissue, and also increases heat shock protein 70 (HSP70) expression. As no study has examined the involvement of intracellular secondary molecules in this setting, the present study compared the renal expressions of HSP70, HMGB1, iNOS, and nitrotyrosine between mice suffered from severe malaria and normal mice. METHODS C57BL/6 mice were divided into an infected group (intraperitoneal injection of 10 6 P. berghei ANKA) and a non-infected group. Renal damage was evaluated using hematoxylin eosin staining, and immunohistochemistry was used to evaluate the expressions of HSP70, HMGB1, iNOS, and nitrotyrosine. RESULTS Significant inter-group differences were observed in the renal expressions of HSP70, HMGB1, and iNOS (p=0.000, Mann-Whitney test), as well as nitrotyrosine (p=0.000, independent t test). The expressions of HSP70 and HMGB1 were strongly correlated (p=0.000, R=1.000). No correlations were observed between iNOS and HMGB, HMGB1 and nitrotyrosine, HSP70 and nitrotyrosine, or iNOS and nitrotyrosine. CONCLUSIONS It appears that HMGB1, HSP70, iNOS, and nitrotyrosine play roles in the renal damage that is observed in mice with severe malaria. Only HSP70 expression is strongly correlated with the expression of HMGB1.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822017000400489&lng=en&tlng=enHMGB1HSP70iNOSNitrotyrosineSevere malaria |
spellingShingle | Loeki Enggar Fitri Ervina Rosmarwati Yesita Rizky Niniek Budiarti Nur Samsu Karyono Mintaroem Strong renal expression of heat shock protein 70, high mobility group box 1, inducible nitric oxide synthase, and nitrotyrosine in mice model of severe malaria Revista da Sociedade Brasileira de Medicina Tropical HMGB1 HSP70 iNOS Nitrotyrosine Severe malaria |
title | Strong renal expression of heat shock protein 70, high mobility group box 1, inducible nitric oxide synthase, and nitrotyrosine in mice model of severe malaria |
title_full | Strong renal expression of heat shock protein 70, high mobility group box 1, inducible nitric oxide synthase, and nitrotyrosine in mice model of severe malaria |
title_fullStr | Strong renal expression of heat shock protein 70, high mobility group box 1, inducible nitric oxide synthase, and nitrotyrosine in mice model of severe malaria |
title_full_unstemmed | Strong renal expression of heat shock protein 70, high mobility group box 1, inducible nitric oxide synthase, and nitrotyrosine in mice model of severe malaria |
title_short | Strong renal expression of heat shock protein 70, high mobility group box 1, inducible nitric oxide synthase, and nitrotyrosine in mice model of severe malaria |
title_sort | strong renal expression of heat shock protein 70 high mobility group box 1 inducible nitric oxide synthase and nitrotyrosine in mice model of severe malaria |
topic | HMGB1 HSP70 iNOS Nitrotyrosine Severe malaria |
url | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822017000400489&lng=en&tlng=en |
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