Literature DB >> 24825161

Rho-GTPases as key regulators of T lymphocyte biology.

Abdelhadi Saoudi1, Sahar Kassem1, Anne Dejean1, Guillaume Gaud1.   

Abstract

Rho-GTPases belong to the Ras superfamily and are crucial signal transducing proteins downstream of many receptors. In general, the Rho-GTPases function as molecular switches, cycling between inactive (GDP-bound) and active (GTP-bound) states. The activated GTP bound Rho-GTPases interact with a broad spectrum of effectors to regulate a plethora of biological pathways including cytoskeletal dynamics, motility, cytokinesis, cell growth, apoptosis, transcriptional activity and nuclear signaling. Recently, gene targeting in mice allowed the selective inactivation of different Rho-GTPases and has advanced our understanding of the physiological role of these proteins, particularly in the immune system. Particularly, these proteins are key signaling molecules in T lymphocytes, which are generated in the thymus and are major players in the immune system. The scope of this review is to discuss recent data obtained in Rho-GTPases deficient mice by focusing on the role-played by Rho-GTPases in T-lymphocyte development, migration, activation and differentiation.

Entities:  

Keywords:  Rho-GTPases; T-cell development; T-cell differentiation; T-cell migration

Mesh:

Substances:

Year:  2014        PMID: 24825161      PMCID: PMC4160340          DOI: 10.4161/sgtp.28208

Source DB:  PubMed          Journal:  Small GTPases        ISSN: 2154-1248


  92 in total

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Journal:  Small GTPases       Date:  2015-06-25

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3.  A large Rab GTPase family in a small GTPase world.

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5.  Splicing factor SRSF1 limits IFN-γ production via RhoH and ameliorates experimental nephritis.

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6.  Small GTPases of the Ras superfamily and glycogen phosphorylase regulation in T cells.

Authors:  Francisco Llavero; Alazne Arrazola Sastre; Miriam Luque Montoro; Miguel A Martín; Joaquín Arenas; Alejandro Lucia; José L Zugaza
Journal:  Small GTPases       Date:  2019-09-12

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8.  A genome-scale gain-of-function CRISPR screen in CD8 T cells identifies proline metabolism as a means to enhance CAR-T therapy.

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Review 10.  Using Murine Models to Investigate Tumor-Lymphoid Interactions: Spotlight on Chronic Lymphocytic Leukemia and Angioimmunoblastic T-Cell Lymphoma.

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