Peptide Bbeta(15-42) preserves endothelial barrier function in shock.
Loss of vascular barrier function causes leak of fluid and proteins into tissues, extensive leak leads to shock and death. Barriers are largely formed by endothelial cell-cell contacts built up by VE-cadherin and are under the control of RhoGTPases. Here we show that a natural plasmin digest product...
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Public Library of Science (PLoS)
2009
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oai:doaj.org-article:5e3eace05f4644b8a7d4e2a5920d49402021-11-25T06:22:58ZPeptide Bbeta(15-42) preserves endothelial barrier function in shock.1932-620310.1371/journal.pone.0005391https://doaj.org/article/5e3eace05f4644b8a7d4e2a5920d49402009-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19401765/?tool=EBIhttps://doaj.org/toc/1932-6203Loss of vascular barrier function causes leak of fluid and proteins into tissues, extensive leak leads to shock and death. Barriers are largely formed by endothelial cell-cell contacts built up by VE-cadherin and are under the control of RhoGTPases. Here we show that a natural plasmin digest product of fibrin, peptide Bbeta15-42 (also called FX06), significantly reduces vascular leak and mortality in animal models for Dengue shock syndrome. The ability of Bbeta15-42 to preserve endothelial barriers is confirmed in rats i.v.-injected with LPS. In endothelial cells, Bbeta15-42 prevents thrombin-induced stress fiber formation, myosin light chain phosphorylation and RhoA activation. The molecular key for the protective effect of Bbeta15-42 is the src kinase Fyn, which associates with VE-cadherin-containing junctions. Following exposure to Bbeta15-42 Fyn dissociates from VE-cadherin and associates with p190RhoGAP, a known antagonists of RhoA activation. The role of Fyn in transducing effects of Bbeta15-42 is confirmed in Fyn(-/-) mice, where the peptide is unable to reduce LPS-induced lung edema, whereas in wild type littermates the peptide significantly reduces leak. Our results demonstrate a novel function for Bbeta15-42. Formerly mainly considered as a degradation product occurring after fibrin inactivation, it has now to be considered as a signaling molecule. It stabilizes endothelial barriers and thus could be an attractive adjuvant in the treatment of shock.Marion GrögerWaltraud PasteinerGeorge IgnatyevUlrich MattSylvia KnappAlena AtrasheuskayaEugenij BukinPeter FriedlDaniela ZinklRenate Hofer-WarbinekKai ZacharowskiPeter PetzelbauerSonja ReingruberPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 4, Iss 4, p e5391 (2009) |
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Medicine R Science Q |
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Medicine R Science Q Marion Gröger Waltraud Pasteiner George Ignatyev Ulrich Matt Sylvia Knapp Alena Atrasheuskaya Eugenij Bukin Peter Friedl Daniela Zinkl Renate Hofer-Warbinek Kai Zacharowski Peter Petzelbauer Sonja Reingruber Peptide Bbeta(15-42) preserves endothelial barrier function in shock. |
| description |
Loss of vascular barrier function causes leak of fluid and proteins into tissues, extensive leak leads to shock and death. Barriers are largely formed by endothelial cell-cell contacts built up by VE-cadherin and are under the control of RhoGTPases. Here we show that a natural plasmin digest product of fibrin, peptide Bbeta15-42 (also called FX06), significantly reduces vascular leak and mortality in animal models for Dengue shock syndrome. The ability of Bbeta15-42 to preserve endothelial barriers is confirmed in rats i.v.-injected with LPS. In endothelial cells, Bbeta15-42 prevents thrombin-induced stress fiber formation, myosin light chain phosphorylation and RhoA activation. The molecular key for the protective effect of Bbeta15-42 is the src kinase Fyn, which associates with VE-cadherin-containing junctions. Following exposure to Bbeta15-42 Fyn dissociates from VE-cadherin and associates with p190RhoGAP, a known antagonists of RhoA activation. The role of Fyn in transducing effects of Bbeta15-42 is confirmed in Fyn(-/-) mice, where the peptide is unable to reduce LPS-induced lung edema, whereas in wild type littermates the peptide significantly reduces leak. Our results demonstrate a novel function for Bbeta15-42. Formerly mainly considered as a degradation product occurring after fibrin inactivation, it has now to be considered as a signaling molecule. It stabilizes endothelial barriers and thus could be an attractive adjuvant in the treatment of shock. |
| format |
article |
| author |
Marion Gröger Waltraud Pasteiner George Ignatyev Ulrich Matt Sylvia Knapp Alena Atrasheuskaya Eugenij Bukin Peter Friedl Daniela Zinkl Renate Hofer-Warbinek Kai Zacharowski Peter Petzelbauer Sonja Reingruber |
| author_facet |
Marion Gröger Waltraud Pasteiner George Ignatyev Ulrich Matt Sylvia Knapp Alena Atrasheuskaya Eugenij Bukin Peter Friedl Daniela Zinkl Renate Hofer-Warbinek Kai Zacharowski Peter Petzelbauer Sonja Reingruber |
| author_sort |
Marion Gröger |
| title |
Peptide Bbeta(15-42) preserves endothelial barrier function in shock. |
| title_short |
Peptide Bbeta(15-42) preserves endothelial barrier function in shock. |
| title_full |
Peptide Bbeta(15-42) preserves endothelial barrier function in shock. |
| title_fullStr |
Peptide Bbeta(15-42) preserves endothelial barrier function in shock. |
| title_full_unstemmed |
Peptide Bbeta(15-42) preserves endothelial barrier function in shock. |
| title_sort |
peptide bbeta(15-42) preserves endothelial barrier function in shock. |
| publisher |
Public Library of Science (PLoS) |
| publishDate |
2009 |
| url |
https://doaj.org/article/5e3eace05f4644b8a7d4e2a5920d4940 |
| work_keys_str_mv |
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