Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
1998-12-7
pubmed:abstractText
Src homology-2 domain-containing inositol polyphosphate 5'-phosphatase (SHIP) is a recently identified protein that has been implicated as an important signaling molecule. Although SHIP has been shown to participate in the FcgammaRIIB-mediated inhibitory signal, the functional role of SHIP in activation responses by immunoreceptor tyrosine-based activation motif-bearing receptors such as B cell receptor (BCR) remains unclear. Indeed, it has been proposed that SHIP serves as a linking molecule for the regulation of the extracellular signal-regulated kinase pathway in BCR signaling, because SHIP associates with Shc. We now report that SHIP-deficient DT40 B cells display enhanced Ca2+ mobilization in response to BCR ligation, whereas extracellular signal-regulated kinase activation is unaffected. This Ca2+ enhancement is due to a sustained intracellular Ca2+ increase or to long-lasting Ca2+ oscillations by loss of SHIP, as revealed by single-cell Ca2+ imaging analysis. These results demonstrate the importance of SHIP in B cell activation by the modulation of Ca2+ mobilization.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD, http://linkedlifedata.com/resource/pubmed/chemical/Calcium, http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels, http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Calmodulin-Dependent..., http://linkedlifedata.com/resource/pubmed/chemical/Fc gamma receptor IIB, http://linkedlifedata.com/resource/pubmed/chemical/INPPL1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/ITPR1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Inositol 1,4,5-Trisphosphate, http://linkedlifedata.com/resource/pubmed/chemical/Inositol 1,4,5-Trisphosphate..., http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Phosphoric Monoester Hydrolases, 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/Receptors, Antigen, T-Cell, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cytoplasmic and Nuclear, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, IgG, http://linkedlifedata.com/resource/pubmed/chemical/antigen T cell receptor, zeta chain
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
161
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5129-32
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:9820480-Animals, pubmed-meshheading:9820480-Antigens, CD, pubmed-meshheading:9820480-B-Lymphocytes, pubmed-meshheading:9820480-Calcium, pubmed-meshheading:9820480-Calcium Channels, pubmed-meshheading:9820480-Calcium Signaling, pubmed-meshheading:9820480-Calcium-Calmodulin-Dependent Protein Kinases, pubmed-meshheading:9820480-Cell Line, pubmed-meshheading:9820480-Chickens, pubmed-meshheading:9820480-Enzyme Activation, pubmed-meshheading:9820480-Inositol 1,4,5-Trisphosphate, pubmed-meshheading:9820480-Inositol 1,4,5-Trisphosphate Receptors, pubmed-meshheading:9820480-Membrane Proteins, pubmed-meshheading:9820480-Phosphoric Monoester Hydrolases, pubmed-meshheading:9820480-Protein Binding, pubmed-meshheading:9820480-Protein-Tyrosine Kinases, pubmed-meshheading:9820480-Receptors, Antigen, B-Cell, pubmed-meshheading:9820480-Receptors, Antigen, T-Cell, pubmed-meshheading:9820480-Receptors, Cytoplasmic and Nuclear, pubmed-meshheading:9820480-Receptors, IgG, pubmed-meshheading:9820480-Transfection, pubmed-meshheading:9820480-src Homology Domains
pubmed:year
1998
pubmed:articleTitle
Role of the inositol phosphatase SHIP in B cell receptor-induced Ca2+ oscillatory response.
pubmed:affiliation
Department of Molecular Genetics, Institute for Liver Research, Kansai Medical University, Moriguchi, Japan.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't