Exogenous glycosyl phosphatidylinositol-anchored CD59 associates with kinases in membrane clusters on U937 cells and becomes Ca(2+)-signaling competent.
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The specificity for the differentiation blocking activity of carcinoembryonic antigen resides in its glycophosphatidyl-inositol anchorUrokinase receptor is associated with the components of the JAK1/STAT1 signaling pathway and leads to activation of this pathway upon receptor clustering in the human kidney epithelial tumor cell line TCL-598Functional heterogeneity of Thy-1 membrane microdomains in rat basophilic leukemia cells.Glycosylphosphatidylinositol-anchor intermediates associate with triton-insoluble membranes in subcellular compartments that include the endoplasmic reticulum.Evidence for budding of human immunodeficiency virus type 1 selectively from glycolipid-enriched membrane lipid rafts.Targeting of functional antibody-CD59 fusion proteins to a cell surface.Plasma membrane rafts play a critical role in HIV-1 assembly and release.Identification of a Naegleria fowleri membrane protein reactive with anti-human CD59 antibody.High-resolution FRET microscopy of cholera toxin B-subunit and GPI-anchored proteins in cell plasma membranesThe roles of membrane microdomains (rafts) in T cell activation.Formation of functional cell membrane domains: the interplay of lipid- and protein-mediated interactions.Control of immune responses by trafficking cell surface proteins, vesicles and lipid rafts to and from the immunological synapse.Microvesicles/exosomes as potential novel biomarkers of metabolic diseasesEndocytosis of GPI-anchored proteins in human lymphocytes: role of glycolipid-based domains, actin cytoskeleton, and protein kinases.Clustered folate receptors deliver 5-methyltetrahydrofolate to cytoplasm of MA104 cells.Exclusion of CD45 inhibits activity of p56lck associated with glycolipid-enriched membrane domains.Polyunsaturated fatty acids inhibit T cell signal transduction by modification of detergent-insoluble membrane domainsA chemical approach to unraveling the biological function of the glycosylphosphatidylinositol anchor.Microdomain-dependent regulation of Lck and Fyn protein-tyrosine kinases in T lymphocyte plasma membranes.Melanoma cells constitutively release an anchor-positive soluble form of protectin (sCD59) that retains functional activities in homologous complement-mediated cytotoxicity.Novel applications for glycosylphosphatidylinositol-anchored proteins in pharmaceutical and industrial biotechnology.Synthetic cell surface receptors for delivery of therapeutics and probes.Properties of exogenously added GPI-anchored proteins following their incorporation into cells.Expression of glycosylphosphatidylinositol-anchored CD59 on target cells enhances human NK cell-mediated cytotoxicitySpecific inhibition of GPI-anchored protein function by homing and self-association of specific GPI anchors.Lipid-assisted microinjection: introducing material into the cytosol and membranes of small cells.Artificially lipid-anchored proteins can elicit clustering-induced intracellular signaling events in Jurkat T-lymphocytes independent of lipid raft association.The channel-forming toxin aerolysin neutralizes human immunodeficiency virus type 1.Protection of human breast cancer cells from complement-mediated lysis by expression of heterologous CD59.Antibody cross-linking of the glycosylphosphatidylinositol-linked protein CD59 on hematopoietic cells induces signaling pathways resembling activation by complement.Signal transduction via glycosyl phosphatidylinositol-anchored proteins in T cells is inhibited by lowering cellular cholesterol.Cutting edge: murine CD59a modulates antiviral CD4+ T cell activity in a complement-independent mannerTransfer of the glycosylphosphatidylinositol-anchored 5'-nucleotidase CD73 from adiposomes into rat adipocytes stimulates lipid synthesis.Inhibition of lipolysis by adiposomes containing glycosylphosphatidylinositol-anchored Gce1 protein in rat adipocytes.Tears contain the complement regulator CD59 as well as decay-accelerating factor (DAF).Incorporation of Artificial Lipid-Anchored Proteins into Cultured Mammalian Cells.CD59 polymorphisms are associated with gene expression and different sexual susceptibility to pemphigus foliaceus.The complement regulatory proteins CD55 (decay accelerating factor) and CD59 are expressed on the inner acrosomal membrane of human spermatozoa as well as CD46 (membrane cofactor protein).The Glycosylation of the Complement Regulatory Protein, Human Erythrocyte CD59
P2860
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P2860
Exogenous glycosyl phosphatidylinositol-anchored CD59 associates with kinases in membrane clusters on U937 cells and becomes Ca(2+)-signaling competent.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Exogenous glycosyl phosphatidy ...... es Ca(2+)-signaling competent.
@en
type
label
Exogenous glycosyl phosphatidy ...... es Ca(2+)-signaling competent.
@en
prefLabel
Exogenous glycosyl phosphatidy ...... es Ca(2+)-signaling competent.
@en
P2093
P2860
P356
P1476
Exogenous glycosyl phosphatidy ...... es Ca(2+)-signaling competent.
@en
P2093
B P Morgan
C W van den Berg
M B Hallett
P2860
P304
P356
10.1083/JCB.131.3.669
P407
P577
1995-11-01T00:00:00Z