Evolution of primary hemostasis in early vertebrates.

Hemostasis is a defense mechanism which protects the organism in the event of injury to stop bleeding. Recently, we established that all the known major mammalian hemostatic factors are conserved in early vertebrates. However, since their highly vascularized gills experience high blood pressure and...

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Main Authors: Seongcheol Kim, Maira Carrillo, Vrinda Kulkarni, Pudur Jagadeeswaran
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-12-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2793433?pdf=render
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spelling doaj-df918de81244475799d241b7513ae64b2020-11-24T21:52:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-12-01412e840310.1371/journal.pone.0008403Evolution of primary hemostasis in early vertebrates.Seongcheol KimMaira CarrilloVrinda KulkarniPudur JagadeeswaranHemostasis is a defense mechanism which protects the organism in the event of injury to stop bleeding. Recently, we established that all the known major mammalian hemostatic factors are conserved in early vertebrates. However, since their highly vascularized gills experience high blood pressure and are exposed to the environment, even very small injuries could be fatal to fish. Since trypsins are forerunners for coagulation proteases and are expressed by many extrapancreatic cells such as endothelial cells and epithelial cells, we hypothesized that trypsin or trypsin-like proteases from gill epithelial cells may protect these animals from gill bleeding following injuries. In this paper we identified the release of three different trypsins from fish gills into water under stress or injury, which have tenfold greater serine protease activity compared to bovine trypsin. We found that these trypsins activate the thrombocytes and protect the fish from gill bleeding. We found 27 protease-activated receptors (PARs) by analyzing zebrafish genome and classified them into five groups, based on tethering peptides, and two families, PAR1 and PAR2, based on homologies. We also found a canonical member of PAR2 family, PAR2-21A which is activated more readily by trypsin, and PAR2-21A tethering peptide stops gill bleeding just as trypsin. This finding provides evidence that trypsin cleaves a PAR2 member on thrombocyte surface. In conclusion, we believe that the gills are evolutionarily selected to produce trypsin to activate PAR2 on thrombocyte surface and protect the gills from bleeding. We also speculate that trypsin may also protect the fish from bleeding from other body injuries due to quick contact with the thrombocytes. Thus, this finding provides evidence for the role of trypsins in primary hemostasis in early vertebrates.http://europepmc.org/articles/PMC2793433?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Seongcheol Kim
Maira Carrillo
Vrinda Kulkarni
Pudur Jagadeeswaran
spellingShingle Seongcheol Kim
Maira Carrillo
Vrinda Kulkarni
Pudur Jagadeeswaran
Evolution of primary hemostasis in early vertebrates.
PLoS ONE
author_facet Seongcheol Kim
Maira Carrillo
Vrinda Kulkarni
Pudur Jagadeeswaran
author_sort Seongcheol Kim
title Evolution of primary hemostasis in early vertebrates.
title_short Evolution of primary hemostasis in early vertebrates.
title_full Evolution of primary hemostasis in early vertebrates.
title_fullStr Evolution of primary hemostasis in early vertebrates.
title_full_unstemmed Evolution of primary hemostasis in early vertebrates.
title_sort evolution of primary hemostasis in early vertebrates.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-12-01
description Hemostasis is a defense mechanism which protects the organism in the event of injury to stop bleeding. Recently, we established that all the known major mammalian hemostatic factors are conserved in early vertebrates. However, since their highly vascularized gills experience high blood pressure and are exposed to the environment, even very small injuries could be fatal to fish. Since trypsins are forerunners for coagulation proteases and are expressed by many extrapancreatic cells such as endothelial cells and epithelial cells, we hypothesized that trypsin or trypsin-like proteases from gill epithelial cells may protect these animals from gill bleeding following injuries. In this paper we identified the release of three different trypsins from fish gills into water under stress or injury, which have tenfold greater serine protease activity compared to bovine trypsin. We found that these trypsins activate the thrombocytes and protect the fish from gill bleeding. We found 27 protease-activated receptors (PARs) by analyzing zebrafish genome and classified them into five groups, based on tethering peptides, and two families, PAR1 and PAR2, based on homologies. We also found a canonical member of PAR2 family, PAR2-21A which is activated more readily by trypsin, and PAR2-21A tethering peptide stops gill bleeding just as trypsin. This finding provides evidence that trypsin cleaves a PAR2 member on thrombocyte surface. In conclusion, we believe that the gills are evolutionarily selected to produce trypsin to activate PAR2 on thrombocyte surface and protect the gills from bleeding. We also speculate that trypsin may also protect the fish from bleeding from other body injuries due to quick contact with the thrombocytes. Thus, this finding provides evidence for the role of trypsins in primary hemostasis in early vertebrates.
url http://europepmc.org/articles/PMC2793433?pdf=render
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