Source:http://linkedlifedata.com/resource/pubmed/id/11404384
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2001-6-13
|
pubmed:abstractText |
Endotoxin-responsive (C3H/HeN) and -hyporesponsive (C3H/HeJ) murine B lymphocytes purified by adherence to anti-immunoglobulin ("antibody panning") possess identical gangliosides but different ganglioside surface accessibilities. We investigated the distribution and surface accessibility of gangliosides of B lymphocytes purified by adherence to plastic ("plastic panning") or by subtraction of non-B-lymphocyte components. As with antibody panning, there were no entirely new or absent gangliosides in plastic-panned or subtraction-purified B lymphocytes of each strain. However, striking changes in relative expression of five gangliosides were detected with each purification protocol. Moreover, five gangliosides of antibody-panned and plastic-panned B lymphocytes but only two gangliosides of subtraction-purified B lymphocytes were inaccessible to surface labeling. Unlike the situation for antibody-panned B lymphocytes, no interstrain (HeN vs. HeJ) surface accessibility differences existed in gangliosides of plastic-panned or subtraction-purified cells. Exposure of subtraction-purified B lymphocytes to anti-immunoglobulin failed to elicit changes in ganglioside expression. Murine B lymphocytes have distinct protocol-dependent differences in glycolipid phenotype which likely denote individual subpopulations.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Endotoxins,
http://linkedlifedata.com/resource/pubmed/chemical/Gangliosides,
http://linkedlifedata.com/resource/pubmed/chemical/Plastics,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, B-Cell,
http://linkedlifedata.com/resource/pubmed/chemical/Sialic Acids
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0741-5400
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
69
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
969-76
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:11404384-Animals,
pubmed-meshheading:11404384-B-Lymphocyte Subsets,
pubmed-meshheading:11404384-Cell Adhesion,
pubmed-meshheading:11404384-Cell Separation,
pubmed-meshheading:11404384-Chromatography, Thin Layer,
pubmed-meshheading:11404384-Endotoxemia,
pubmed-meshheading:11404384-Endotoxins,
pubmed-meshheading:11404384-Gangliosides,
pubmed-meshheading:11404384-Genetic Predisposition to Disease,
pubmed-meshheading:11404384-Immunity, Innate,
pubmed-meshheading:11404384-Mice,
pubmed-meshheading:11404384-Mice, Inbred C3H,
pubmed-meshheading:11404384-Plastics,
pubmed-meshheading:11404384-Receptors, Antigen, B-Cell,
pubmed-meshheading:11404384-Sialic Acids,
pubmed-meshheading:11404384-Spleen
|
pubmed:year |
2001
|
pubmed:articleTitle |
Differences in splenic B-lymphocyte ganglioside expression and accessibility in normal and endotoxin-hyporesponsive mice.
|
pubmed:affiliation |
Infectious Diseases Section, Department of Veterans Affairs Western New York Healthcare System and State University of New York at Buffalo, Buffalo, New York, USA. berenson@acsu.buffalo.edu
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, Non-P.H.S.
|