Microbe-specific C3b deposition in the horseshoe crab complement system in a C2/factor B-dependent or -independent manner.

Complement C3 plays an essential role in the opsonization of pathogens in the mammalian complement system, whereas the molecular mechanism underlying C3 activation in invertebrates remains unknown. To understand the molecular mechanism of C3b deposition on microbes, we characterized two types of C2/...

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Autores principales: Keisuke Tagawa, Toyoki Yoshihara, Toshio Shibata, Kazuki Kitazaki, Yuichi Endo, Teizo Fujita, Takumi Koshiba, Shun-ichiro Kawabata
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:71b38c3d9df1403fb3947e4a14d755052021-11-18T07:19:26ZMicrobe-specific C3b deposition in the horseshoe crab complement system in a C2/factor B-dependent or -independent manner.1932-620310.1371/journal.pone.0036783https://doaj.org/article/71b38c3d9df1403fb3947e4a14d755052012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22611464/?tool=EBIhttps://doaj.org/toc/1932-6203Complement C3 plays an essential role in the opsonization of pathogens in the mammalian complement system, whereas the molecular mechanism underlying C3 activation in invertebrates remains unknown. To understand the molecular mechanism of C3b deposition on microbes, we characterized two types of C2/factor B homologs (designated TtC2/Bf-1 and TtC2/Bf-2) identified from the horseshoe crab Tachypleus tridentatus. Although the domain architectures of TtC2/Bf-1 and TtC2/Bf-2 were identical to those of mammalian homologs, they contained five-repeated and seven-repeated complement control protein domains at their N-terminal regions, respectively. TtC2/Bf-1 and TtC2/Bf-2 were synthesized and glycosylated in hemocytes and secreted to hemolymph plasma, which existed in a complex with C3 (TtC3), and their activation by microbes was absolutely Mg(2+)-dependent. Flow cytometric analysis revealed that TtC3b deposition was Mg(2+)-dependent on Gram-positive bacteria or fungi, but not on Gram-negative bacteria. Moreover, this analysis demonstrated that Ca(2+)-dependent lectins (C-reactive protein-1 and tachylectin-5A) were required for TtC3b deposition on Gram-positive bacteria, and that a Ca(2+)-independent lectin (Tachypleus plasma lectin-1) was definitely indispensable for TtC3b deposition on fungi. In contrast, a horseshoe crab lipopolysaccharide-sensitive protease factor C was necessary and sufficient to deposit TtC3b on Gram-negative bacteria. We conclude that plasma lectins and factor C play key roles in microbe-specific TtC3b deposition in a C2/factor B-dependent or -independent manner.Keisuke TagawaToyoki YoshiharaToshio ShibataKazuki KitazakiYuichi EndoTeizo FujitaTakumi KoshibaShun-ichiro KawabataPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 5, p e36783 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Keisuke Tagawa
Toyoki Yoshihara
Toshio Shibata
Kazuki Kitazaki
Yuichi Endo
Teizo Fujita
Takumi Koshiba
Shun-ichiro Kawabata
Microbe-specific C3b deposition in the horseshoe crab complement system in a C2/factor B-dependent or -independent manner.
description Complement C3 plays an essential role in the opsonization of pathogens in the mammalian complement system, whereas the molecular mechanism underlying C3 activation in invertebrates remains unknown. To understand the molecular mechanism of C3b deposition on microbes, we characterized two types of C2/factor B homologs (designated TtC2/Bf-1 and TtC2/Bf-2) identified from the horseshoe crab Tachypleus tridentatus. Although the domain architectures of TtC2/Bf-1 and TtC2/Bf-2 were identical to those of mammalian homologs, they contained five-repeated and seven-repeated complement control protein domains at their N-terminal regions, respectively. TtC2/Bf-1 and TtC2/Bf-2 were synthesized and glycosylated in hemocytes and secreted to hemolymph plasma, which existed in a complex with C3 (TtC3), and their activation by microbes was absolutely Mg(2+)-dependent. Flow cytometric analysis revealed that TtC3b deposition was Mg(2+)-dependent on Gram-positive bacteria or fungi, but not on Gram-negative bacteria. Moreover, this analysis demonstrated that Ca(2+)-dependent lectins (C-reactive protein-1 and tachylectin-5A) were required for TtC3b deposition on Gram-positive bacteria, and that a Ca(2+)-independent lectin (Tachypleus plasma lectin-1) was definitely indispensable for TtC3b deposition on fungi. In contrast, a horseshoe crab lipopolysaccharide-sensitive protease factor C was necessary and sufficient to deposit TtC3b on Gram-negative bacteria. We conclude that plasma lectins and factor C play key roles in microbe-specific TtC3b deposition in a C2/factor B-dependent or -independent manner.
format article
author Keisuke Tagawa
Toyoki Yoshihara
Toshio Shibata
Kazuki Kitazaki
Yuichi Endo
Teizo Fujita
Takumi Koshiba
Shun-ichiro Kawabata
author_facet Keisuke Tagawa
Toyoki Yoshihara
Toshio Shibata
Kazuki Kitazaki
Yuichi Endo
Teizo Fujita
Takumi Koshiba
Shun-ichiro Kawabata
author_sort Keisuke Tagawa
title Microbe-specific C3b deposition in the horseshoe crab complement system in a C2/factor B-dependent or -independent manner.
title_short Microbe-specific C3b deposition in the horseshoe crab complement system in a C2/factor B-dependent or -independent manner.
title_full Microbe-specific C3b deposition in the horseshoe crab complement system in a C2/factor B-dependent or -independent manner.
title_fullStr Microbe-specific C3b deposition in the horseshoe crab complement system in a C2/factor B-dependent or -independent manner.
title_full_unstemmed Microbe-specific C3b deposition in the horseshoe crab complement system in a C2/factor B-dependent or -independent manner.
title_sort microbe-specific c3b deposition in the horseshoe crab complement system in a c2/factor b-dependent or -independent manner.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/71b38c3d9df1403fb3947e4a14d75505
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