In vivo TCR signaling in CD4+ T cells imprints a cell-intrinsic, transient low-motility pattern independent of chemokine receptor expression levels, or microtubular network, integrin, and protein kinase C activity

Frontiers in Immunology

Volumn 6, Issue JUN, 2015, Pages

  Ackerknecht, Markus ^a   Hauser, Mark A ^b   Legler, Daniel F ^b   Stein, Jens V ^a  

^a UNIVERSITY OF BERN   (Switzerland)

^b UNIVERSITY OF KONSTANZ   (Switzerland)

Author keywords

CCR7; CD4+T cell migration; Lymph node; PKC; Stathmin; T cell activation

Indexed keywords

CHEMOKINE RECEPTOR; CHEMOKINE RECEPTOR CCR7; CHEMOKINE RECEPTOR CXCR4; CHEMOKINE RECEPTOR CXCR5; EZRIN; FREUND ADJUVANT; G PROTEIN COUPLED RECEPTOR KINASE; INTEGRIN; INTERCELLULAR ADHESION MOLECULE 1; INTERCELLULAR ADHESION MOLECULE 2; L SELECTIN; MACROPHAGE INFLAMMATORY PROTEIN 3BETA; MOESIN; NOCODAZOLE; OVALBUMIN; PROTEIN KINASE C; RADIXIN; SECONDARY LYMPHOID TISSUE CHEMOKINE; STATHMIN; T LYMPHOCYTE RECEPTOR; THROMBOXANE A2;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CD4+ T LYMPHOCYTE; CELL MIGRATION ASSAY; CELL MOTILITY; CELL POPULATION; CHEMOTAXIS ASSAY; CONTROLLED STUDY; ENZYME ACTIVITY; FLOW CYTOMETRY; IMMUNIZATION; IMMUNOFLUORESCENCE TEST; INFLAMMATION; INTRACELLULAR SIGNALING; LYMPH NODE; MAJOR HISTOCOMPATIBILITY COMPLEX; MICROTUBULE; MOUSE; NONHUMAN; PHOSPHORYLATION; PROTEIN EXPRESSION; WESTERN BLOTTING;

EID: 84935146520     PISSN: None     EISSN: 16643224     Source Type: Journal    
DOI: 10.3389/fimmu.2015.00297     Document Type: Article

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