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Rapid clearance of malaria circumsporozoite protein (CS) by hepatocytes

The circumsporozoite protein (CS) covers uniformly the plasma membrane of malaria sporozoites. In vitro, CS multimers bind specifically to regions of the hepatocyte plasma membrane that are exposed to circulating blood in the Disse space. The ligand is in the region II- plus of CS, an evolutionarily...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191367/
https://www.ncbi.nlm.nih.gov/pubmed/8294876
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description The circumsporozoite protein (CS) covers uniformly the plasma membrane of malaria sporozoites. In vitro, CS multimers bind specifically to regions of the hepatocyte plasma membrane that are exposed to circulating blood in the Disse space. The ligand is in the region II- plus of CS, an evolutionarily conserved stretch of the protein that has amino acid sequence homology to a cell adhesive motif of thrombospondin. We have now found that intravenously injected CS constructs bind rapidly to the basolateral surface of hepatocytes, provided that the recombinant proteins contain region II-plus, and that they are aggregated. Significant amounts of CS were not retained in any other organ. The striking parallelism between these in vitro and in vivo findings with the target specificity of malaria sporozoites, reinforces the hypothesis that the attachment of the parasites to hepatocytes is via region II-plus of CS.
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spelling pubmed-21913672008-04-16 Rapid clearance of malaria circumsporozoite protein (CS) by hepatocytes J Exp Med Articles The circumsporozoite protein (CS) covers uniformly the plasma membrane of malaria sporozoites. In vitro, CS multimers bind specifically to regions of the hepatocyte plasma membrane that are exposed to circulating blood in the Disse space. The ligand is in the region II- plus of CS, an evolutionarily conserved stretch of the protein that has amino acid sequence homology to a cell adhesive motif of thrombospondin. We have now found that intravenously injected CS constructs bind rapidly to the basolateral surface of hepatocytes, provided that the recombinant proteins contain region II-plus, and that they are aggregated. Significant amounts of CS were not retained in any other organ. The striking parallelism between these in vitro and in vivo findings with the target specificity of malaria sporozoites, reinforces the hypothesis that the attachment of the parasites to hepatocytes is via region II-plus of CS. The Rockefeller University Press 1994-02-01 /pmc/articles/PMC2191367/ /pubmed/8294876 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Rapid clearance of malaria circumsporozoite protein (CS) by hepatocytes
title Rapid clearance of malaria circumsporozoite protein (CS) by hepatocytes
title_full Rapid clearance of malaria circumsporozoite protein (CS) by hepatocytes
title_fullStr Rapid clearance of malaria circumsporozoite protein (CS) by hepatocytes
title_full_unstemmed Rapid clearance of malaria circumsporozoite protein (CS) by hepatocytes
title_short Rapid clearance of malaria circumsporozoite protein (CS) by hepatocytes
title_sort rapid clearance of malaria circumsporozoite protein (cs) by hepatocytes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191367/
https://www.ncbi.nlm.nih.gov/pubmed/8294876