Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2003-1-6
pubmed:abstractText
Plasmodium sporozoites are transmitted through the bite of infected mosquitoes and first invade the liver of the mammalian host, as an obligatory step of the life cycle of the malaria parasite. Within hepatocytes, Plasmodium sporozoites reside in a membrane-bound vacuole, where they differentiate into exoerythrocytic forms and merozoites that subsequently infect erythrocytes and cause the malaria disease. Plasmodium sporozoite targeting to the liver is mediated by the specific binding of major sporozoite surface proteins, the circumsporozoite protein and the thrombospondin-related anonymous protein, to glycosaminoglycans on the hepatocyte surface. Still, the molecular mechanisms underlying sporozoite entry and differentiation within hepatocytes are largely unknown. Here we show that the tetraspanin CD81, a putative receptor for hepatitis C virus, is required on hepatocytes for human Plasmodium falciparum and rodent Plasmodium yoelii sporozoite infectivity. P. yoelii sporozoites fail to infect CD81-deficient mouse hepatocytes, in vivo and in vitro, and antibodies against mouse and human CD81 inhibit in vitro the hepatic development of P. yoelii and P. falciparum, respectively. We further demonstrate that the requirement for CD81 is linked to sporozoite entry into hepatocytes by formation of a parasitophorous vacuole, which is essential for parasite differentiation into exoerythrocytic forms.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD81, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD9, http://linkedlifedata.com/resource/pubmed/chemical/CD81 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CD9 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Cd81 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Cd9 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Protozoan Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins, http://linkedlifedata.com/resource/pubmed/chemical/circumsporozoite protein, Protozoan
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1078-8956
pubmed:author
pubmed:issnType
Print
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
93-6
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:12483205-Animals, pubmed-meshheading:12483205-Anopheles, pubmed-meshheading:12483205-Antigens, CD, pubmed-meshheading:12483205-Antigens, CD81, pubmed-meshheading:12483205-Antigens, CD9, pubmed-meshheading:12483205-Cells, Cultured, pubmed-meshheading:12483205-Hepatocytes, pubmed-meshheading:12483205-Humans, pubmed-meshheading:12483205-Malaria, pubmed-meshheading:12483205-Malaria, Falciparum, pubmed-meshheading:12483205-Membrane Glycoproteins, pubmed-meshheading:12483205-Membrane Proteins, pubmed-meshheading:12483205-Mice, pubmed-meshheading:12483205-Mice, Inbred BALB C, pubmed-meshheading:12483205-Mice, Inbred C57BL, pubmed-meshheading:12483205-Mice, Knockout, pubmed-meshheading:12483205-Plasmodium falciparum, pubmed-meshheading:12483205-Plasmodium yoelii, pubmed-meshheading:12483205-Protozoan Proteins, pubmed-meshheading:12483205-Recombinant Fusion Proteins, pubmed-meshheading:12483205-Sporozoites
pubmed:year
2003
pubmed:articleTitle
Hepatocyte CD81 is required for Plasmodium falciparum and Plasmodium yoelii sporozoite infectivity.
pubmed:affiliation
INSERM U511 Immunobiologie Cellulaire et Moléculaire des Infections Parasitaires, Centre Hospitalo-Universitaire Pitié-Salpêtrière, Université Pierre et Marie Curie, Paris, France.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't