Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
1989-10-17
pubmed:abstractText
Class I major histocompatibility complex proteins appear to be the major cell surface receptors for simian virus 40 (SV40), as implied by the following observations. Adsorption of SV40 to LLC-MK2 rhesus monkey kidney cells specifically inhibited binding of a monoclonal antibody (MAb) against class I human lymphocyte antigen (HLA) proteins. Conversely, pretreatment of LLC-MK2 cells with anti-HLA MAbs inhibited infection by SV40. The ability of anti-HLA to inhibit infection was greatly reduced when the order of addition of the anti-HLA and the virus was reversed. Infection was also inhibited by preincubating SV40 with purified soluble class I protein. Finally, human lymphoblastoid cells of the Daudi line, which do not express class I major histocompatibility complex proteins, were infected at relatively low levels with SV40 virions. In a control experiment, we found that pretreatment of cells with a MAb specific for the leukocytic-function-associated antigen LFA-3 actually enhanced infection. This finding may also support the premise that class I major histocompatibility complex proteins are receptors for SV40.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-11894933, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-13774265, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-176470, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-219235, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2536142, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2536822, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2538240, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2538243, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2538244, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2538245, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2541915, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2823150, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2827378, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2835857, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2840661, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-2993920, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-3263576, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-3289571, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-3309949, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-3374584, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-6083454, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-6096719, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-6187124, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-6255675, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-6298589, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-6313808, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-6345670, http://linkedlifedata.com/resource/pubmed/commentcorrection/2476575-92183
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0022-538X
pubmed:author
pubmed:issnType
Print
pubmed:volume
63
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4474-7
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1989
pubmed:articleTitle
Class I major histocompatibility proteins as cell surface receptors for simian virus 40.
pubmed:affiliation
Graduate Program in Neuroscience and Behavior, University of Massachusetts, Amhers 01003.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't