» Articles » PMID: 20870900

Critical Roles for Rac GTPases in T-cell Migration to and Within Lymph Nodes

Overview
Journal Blood
Publisher Elsevier
Specialty Hematology
Date 2010 Sep 28
PMID 20870900
Citations 41
Authors
Affiliations
Soon will be listed here.
Abstract

Naive T cells continuously recirculate between secondary lymphoid tissue via the blood and lymphatic systems, a process that maximizes the chances of an encounter between a T cell and its cognate antigen. This recirculation depends on signals from chemokine receptors, integrins, and the sphingosine-1-phosphate receptor. The authors of previous studies in other cell types have shown that Rac GTPases transduce signals leading to cell migration and adhesion; however, their roles in T cells are unknown. By using both 3-dimensional intravital and in vitro approaches, we show that Rac1- and Rac2-deficient T cells have multiple defects in this recirculation process. Rac-deficient T cells home very inefficiently to lymph nodes and the white pulp of the spleen, show reduced interstitial migration within lymph node parenchyma, and are defective in egress from lymph nodes. These mutant T cells show defective chemokine-induced chemotaxis, chemokinesis, and adhesion to integrin ligands. They have reduced lateral motility on endothelial cells and transmigrate in-efficiently. These multiple defects stem from critical roles for Rac1 and Rac2 in transducing chemokine and sphingosine-1-phosphate receptor 1 signals leading to motility and adhesion.

Citing Articles

Vascular Inflammation and Smooth Muscle Contractility: The Role of Nox1-Derived Superoxide and LRRC8 Anion Channels.

Lamb F, Choi H, Miller M, Stark R Hypertension. 2024; 81(4):752-763.

PMID: 38174563 PMC: 10954410. DOI: 10.1161/HYPERTENSIONAHA.123.19434.


Role of Rho GTPases in inflammatory bowel disease.

Li X, Zhang M, Zhou G, Xie Z, Wang Y, Han J Cell Death Discov. 2023; 9(1):24.

PMID: 36690621 PMC: 9871048. DOI: 10.1038/s41420-023-01329-w.


Combined Immunodeficiency Caused by a Novel De Novo Gain-of-Function RAC2 Mutation.

Zhang L, Chen Z, Li W, Liu Q, Wang Y, Chen X J Clin Immunol. 2022; 42(6):1280-1292.

PMID: 35596857 DOI: 10.1007/s10875-022-01288-4.


Single-cell eQTL analysis of activated T cell subsets reveals activation and cell type-dependent effects of disease-risk variants.

Schmiedel B, Gonzalez-Colin C, Fajardo V, Rocha J, Madrigal A, Ramirez-Suastegui C Sci Immunol. 2022; 7(68):eabm2508.

PMID: 35213211 PMC: 9035271. DOI: 10.1126/sciimmunol.abm2508.


The Critical Importance of Spatial and Temporal Scales in Designing and Interpreting Immune Cell Migration Assays.

Frattolin J, Watson D, Bonneuil W, Russell M, Fasanella Masci F, Bandara M Cells. 2021; 10(12).

PMID: 34943947 PMC: 8700135. DOI: 10.3390/cells10123439.


References
1.
Croker B, Tarlinton D, Cluse L, Tuxen A, Light A, Yang F . The Rac2 guanosine triphosphatase regulates B lymphocyte antigen receptor responses and chemotaxis and is required for establishment of B-1a and marginal zone B lymphocytes. J Immunol. 2002; 168(7):3376-86. DOI: 10.4049/jimmunol.168.7.3376. View

2.
Asperti-Boursin F, Real E, Bismuth G, Trautmann A, Donnadieu E . CCR7 ligands control basal T cell motility within lymph node slices in a phosphoinositide 3-kinase-independent manner. J Exp Med. 2007; 204(5):1167-79. PMC: 2118589. DOI: 10.1084/jem.20062079. View

3.
Surh C, Sprent J . Homeostasis of naive and memory T cells. Immunity. 2008; 29(6):848-62. DOI: 10.1016/j.immuni.2008.11.002. View

4.
Woolf E, Grigorova I, Sagiv A, Grabovsky V, Feigelson S, Shulman Z . Lymph node chemokines promote sustained T lymphocyte motility without triggering stable integrin adhesiveness in the absence of shear forces. Nat Immunol. 2007; 8(10):1076-85. DOI: 10.1038/ni1499. View

5.
Guo F, Cancelas J, Hildeman D, Williams D, Zheng Y . Rac GTPase isoforms Rac1 and Rac2 play a redundant and crucial role in T-cell development. Blood. 2008; 112(5):1767-75. PMC: 2518885. DOI: 10.1182/blood-2008-01-132068. View