CD4 and CD8 T cells require different membrane gangliosides for activation.
about
Lower Affinity T Cells are Critical Components and Active Participants of the Immune ResponseImbalance in fatty-acid-chain length of gangliosides triggers Alzheimer amyloid deposition in the precuneusSystemic blockade of sialylation in mice with a global inhibitor of sialyltransferases.Reducing FLI1 levels in the MRL/lpr lupus mouse model impacts T cell function by modulating glycosphingolipid metabolismGanglioside biochemistryCD8+ T Cells Mediate Female-Dominant IL-4 Production and Airway Inflammation in Allergic Asthma.Role of glycosphingolipids in dendritic cell-mediated HIV-1 trans-infection.Quantitative Proteomic Analysis of Escherichia coli Heat-Labile Toxin B Subunit (LTB) with Enterovirus 71 (EV71) Subunit VP1A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylationNormalizing glycosphingolipids restores function in CD4+ T cells from lupus patients.Crystallization around solid-like nanosized docks can explain the specificity, diversity, and stability of membrane microdomains.Microdomains, Inflammation, and Atherosclerosis.Relative roles of GM1 ganglioside, N-acylneuraminic acids, and α2β1 integrin in mediating rotavirus infection.Membrane microdomains in immunity: glycosphingolipid-enriched domain-mediated innate immune responses.Heterogeneity of gangliosides among T cell subsets.GSL-enriched membrane microdomains in innate immune responses.Recent advances in nontoxic Escherichia coli heat-labile toxin and its derivative adjuvants.TALEN mediated targeted editing of GM2/GD2-synthase gene modulates anchorage independent growth by reducing anoikis resistance in mouse tumor cells.Expression machinery of GM4: the excess amounts of GM3/GM4S synthase (ST3GAL5) are necessary for GM4 synthesis in mammalian cells.FLI1 Levels Impact CXCR3 Expression and Renal Infiltration of T Cells and Renal Glycosphingolipid Metabolism in the MRL/lpr Lupus Mouse Strain.Activation of human naïve Th cells increases surface expression of GD3 and induces neoexpression of GD2 that colocalize with TCR clusters.Properties and functions of lactosylceramide from mouse neutrophils.Lck, Membrane Microdomains, and TCR Triggering Machinery: Defining the New Rules of EngagementTranscriptional Regulation of T-Cell Lipid Metabolism: Implications for Plasma Membrane Lipid Rafts and T-Cell Function.Identification of a new liver-specific c-type mRNA transcriptional variant for mouse ST3GAL5 (GM3/GM4 synthase).Impact of lipid rafts on the T-cell-receptor and peptide-major-histocompatibility-complex interactions under different measurement conditions.Preparation of CD4+ T Cells for Analysis of GD3 and GD2 Ganglioside Membrane Expression by Microscopy.The regulation of ER export and Golgi retention of ST3Gal5 (GM3/GM4 synthase) and B4GalNAcT1 (GM2/GD2/GA2 synthase) by arginine/lysine-based motif adjacent to the transmembrane domain.Influence of APOE genotype and the presence of Alzheimer's pathology on synaptic membrane lipids of human brains.Fresh Evidence for Platelets as Neuronal and Innate Immune Cells: Their Role in the Activation, Differentiation, and Deactivation of Th1, Th17, and Tregs during Tissue Inflammation.
P2860
Q26781296-724FF39E-7D5B-4BC9-BAB1-C125398F9A75Q28544853-DD622EBB-C4A6-4098-AAEB-1210844BE0C5Q34737768-7F624924-914D-4F90-B2FC-5074FD0B2067Q34990559-4B228B44-3569-4FB7-AD30-F4C72A421148Q35361488-E3C92B90-1DF0-49A5-8104-B15A98D178A2Q35815809-6B2EDEB9-5196-4EEB-B457-18364CE52C00Q36940332-E8966924-D3B5-4603-A9FE-5226D32F6A12Q37286320-11946EF8-9E5C-427C-A944-88038CF5AD91Q37406440-6E717544-53D9-4CAB-8410-9F8DE8E83BC6Q37524224-51433870-1E2A-4BB3-8350-B65206C73459Q37618993-D62C6D3C-7470-4412-BE53-E47B36D4036DQ37623996-4ADB24D5-6B2A-4BC0-96BE-10CCBA90C0ACQ37713926-F81E69BE-816B-442C-964D-D4ED5B2DCF8FQ38001407-632123C0-49DD-4278-A60E-01C1B339A79FQ38066785-7FDB8180-633A-4B9A-9FC0-FF949F318E85Q38086070-3CCA3D1F-D6A9-427E-BAE7-426D282E1B0DQ38818721-4B25C118-2145-4A5F-859F-BC6BEE0C280DQ38900943-F4DE2A58-0B9E-496F-BEEB-EAC9BCC9B3A2Q39100973-47E5B3F7-1C71-47C8-AC4C-5F8E2B21CD8BQ41148881-4D23F5C8-340C-4295-9E9E-6BBFCD8EF5E0Q41492798-21752888-A595-49A4-8A72-DD14A48209ECQ41539560-4C372257-A519-4E34-93ED-13182A5B9128Q42069094-2F44C91C-92A0-4E8F-95FC-462B9ED3B756Q47160173-9899305A-1E64-4298-BCE6-5728113B5091Q47951796-9B184364-A3AD-419C-BB97-EEA471CA72BAQ51001267-DD29B28E-BCA9-4E21-BE5A-534043D3D43FQ51031327-DE04D070-3649-4A58-BECA-EDA37BF601ABQ51722538-C9E8A646-3B21-4D9D-BDDF-F671B0A06F62Q53348326-C459BB16-9614-49CD-8B90-6F8E91AB8B10Q55248939-D0DC1C07-47CF-40EF-A3A0-785ED705EB02
P2860
CD4 and CD8 T cells require different membrane gangliosides for activation.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
CD4 and CD8 T cells require different membrane gangliosides for activation.
@ast
CD4 and CD8 T cells require different membrane gangliosides for activation.
@en
type
label
CD4 and CD8 T cells require different membrane gangliosides for activation.
@ast
CD4 and CD8 T cells require different membrane gangliosides for activation.
@en
prefLabel
CD4 and CD8 T cells require different membrane gangliosides for activation.
@ast
CD4 and CD8 T cells require different membrane gangliosides for activation.
@en
P2093
P2860
P356
P1476
CD4 and CD8 T cells require different membrane gangliosides for activation.
@en
P2093
Akemi Suzuki
Jin-ichi Inokuchi
Kaori Okuyama
Katsunori Iwasaki
Masakazu Nagafuku
Michihiro Fujiwara
Motoaki Takayanagi
Tadashi Yamashita
Yuri Onimaru
P2860
P304
P356
10.1073/PNAS.1114965109
P407
P577
2012-01-17T00:00:00Z