DOCK2 is essential for antigen-induced translocation of TCR and lipid rafts, but not PKC-theta and LFA-1, in T cells (Q28593591)

31 January 2017

title

DOCK2 is essential for antigen-induced translocation of TCR and lipid rafts, but not PKC-theta and LFA-1, in T cells (English)

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Dedicator of cyto-kinesis 2

31 January 2017

main subject

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GOA release 2020-03-11

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Yoshinori Fukui

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Terukazu Sanui

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31 January 2017

Ayumi Inayoshi

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31 January 2017

Mayuko Noda

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31 January 2017

Eiko Iwata

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31 January 2017

Masahiro Oike

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31 January 2017

Takehiko Sasazuki

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31 January 2017

language of work or name

English

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publication date

1 July 2003

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31 January 2017

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31 January 2017

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31 January 2017

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31 January 2017

page(s)

119–129

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Distinct patterns of membrane microdomain partitioning in Th1 and th2 cells.

31 January 2017

cites work

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Antigen-induced translocation of PKC-theta to membrane rafts is required for T cell activation

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Unconventional Rac-GEF activity is mediated through the Dock180-ELMO complex

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Haematopoietic cell-specific CDM family protein DOCK2 is essential for lymphocyte migration

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Vav regulates peptide-specific apoptosis in thymocytes

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Human CD8+ T cells do not require the polarization of lipid rafts for activation and proliferation

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Cbl-b is a negative regulator of receptor clustering and raft aggregation in T cells

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Vav1 controls integrin clustering and MHC/peptide-specific cell adhesion to antigen-presenting cells

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DOCK2 mediates T cell receptor-induced activation of Rac2 and IL-2 transcription

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Myoblast city, the Drosophila homolog of DOCK180/CED-5, is required in a Rac signaling pathway utilized for multiple developmental processes

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7 January 2021

The Actin Cytoskeleton and Lymphocyte Activation

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Tyrosine phosphorylation of Pyk2 is selectively regulated by Fyn during TCR signaling

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Defective antigen receptor-mediated proliferation of B and T cells in the absence of Vav.

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A Requirement for the Rho-Family GTP Exchange Factor Vav in Positive and Negative Selection of Thymocytes

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A novel functional interaction between Vav and PKCtheta is required for TCR-induced T cell activation.

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Vav1/Rac-dependent actin cytoskeleton reorganization is required for lipid raft clustering in T cells

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7 January 2021

Translocation of PKC[theta] in T cells is mediated by a nonconventional, PI3-K- and Vav-dependent pathway, but does not absolutely require phospholipase C

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7 January 2021

T lymphocyte costimulation mediated by reorganization of membrane microdomains

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Regulated nuclear import of Rel proteins in the Drosophila immune response

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Vav and SLP-76 interact and functionally cooperate in IL-2 gene activation

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7 January 2021

The vav exchange factor is an essential regulator in actin-dependent receptor translocation to the lymphocyte-antigen-presenting cell interface

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7 January 2021

A receptor/cytoskeletal movement triggered by costimulation during T cell activation

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Visualizing the dynamics of T cell activation: intracellular adhesion molecule 1 migrates rapidly to the T cell/B cell interface and acts to sustain calcium levels

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7 January 2021

Non-CD28 costimulatory molecules present in T cell rafts induce T cell costimulation by enhancing the association of TCR with rafts.

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7 January 2021

Deficiency of small GTPase Rac2 affects T cell activation

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7 January 2021

Defective signalling through the T- and B-cell antigen receptors in lymphoid cells lacking the vav proto-oncogene

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7 January 2021

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017