Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1997-5-13
pubmed:abstractText
It is not known how immunogenic versus tolerogenic cellular responses are signaled by receptors such as the B cell antigen receptor (BCR). Here we compare BCR signaling in naive cells that respond positively to foreign antigen and self-tolerant cells that respond negatively to self-antigen. In naive cells, foreign antigen triggered a large biphasic calcium response and activated nuclear signals through NF-AT, NF-kappa B, JNK, and ERK/pp90rsk. In tolerant B cells, self-antigen stimulated low calcium oscillations and activated NF-AT and ERK/pp90rsk but not NF-kappa B or JNK. Self-reactive B cells lacking the phosphatase CD45 did not exhibit calcium oscillations or ERK/pp90rsk activation, nor did they repond negatively to self-antigen. These data reveal striking biochemical differences in BCR signaling to the nucleus during positive selection by foreign antigens and negative selection by self-antigens.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD45, http://linkedlifedata.com/resource/pubmed/chemical/Calcium, http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Calmodulin-Dependent..., http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Early Growth Response Protein 1, http://linkedlifedata.com/resource/pubmed/chemical/Egr1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Immediate-Early Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 1, http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B, http://linkedlifedata.com/resource/pubmed/chemical/NFATC Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Tyrosine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, B-Cell, http://linkedlifedata.com/resource/pubmed/chemical/Ribosomal Protein S6 Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1074-7613
pubmed:author
pubmed:issnType
Print
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
419-28
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:9133421-Animals, pubmed-meshheading:9133421-Antigens, CD45, pubmed-meshheading:9133421-B-Lymphocytes, pubmed-meshheading:9133421-Biological Transport, pubmed-meshheading:9133421-Calcium, pubmed-meshheading:9133421-Calcium-Calmodulin-Dependent Protein Kinases, pubmed-meshheading:9133421-Cell Nucleus, pubmed-meshheading:9133421-DNA-Binding Proteins, pubmed-meshheading:9133421-Early Growth Response Protein 1, pubmed-meshheading:9133421-Gene Expression Regulation, pubmed-meshheading:9133421-Immediate-Early Proteins, pubmed-meshheading:9133421-Immune Tolerance, pubmed-meshheading:9133421-Mice, pubmed-meshheading:9133421-Mice, Transgenic, pubmed-meshheading:9133421-Mitogen-Activated Protein Kinase 1, pubmed-meshheading:9133421-NF-kappa B, pubmed-meshheading:9133421-NFATC Transcription Factors, pubmed-meshheading:9133421-Nuclear Proteins, pubmed-meshheading:9133421-Protein-Serine-Threonine Kinases, pubmed-meshheading:9133421-Protein-Tyrosine Kinases, pubmed-meshheading:9133421-Receptors, Antigen, B-Cell, pubmed-meshheading:9133421-Ribosomal Protein S6 Kinases, pubmed-meshheading:9133421-Signal Transduction, pubmed-meshheading:9133421-Transcription Factors
pubmed:year
1997
pubmed:articleTitle
Different nuclear signals are activated by the B cell receptor during positive versus negative signaling.
pubmed:affiliation
Department of Microbiology and Immunology, Stanford University School of Medicine, California 94305, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't