Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Loss of Gadkin affects dendritic cell migration in vitro

[img] PDF - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
6MB

Item Type:Article
Title:Loss of Gadkin affects dendritic cell migration in vitro
Creators Name:Schachtner, H. and Weimershaus, M. and Stache, V. and Plewa, N. and Legler, D.F. and Höpken, U.E. and Maritzen, T.
Abstract:Migration is crucial for the function of dendritic cells (DCs), which act as outposts of the immune system. Upon detection of pathogens, skin- and mucosa-resident DCs migrate to secondary lymphoid organs where they activate T cells. DC motility relies critically on the actin cytoskeleton, which is regulated by the actin-related protein 2/3 (ARP2/3) complex, a nucleator of branched actin networks. Consequently, loss of ARP2/3 stimulators and upstream Rho family GTPases dramatically impairs DC migration. However, nothing is known yet about the relevance of ARP2/3 inhibitors for DC migration. We previously demonstrated that the AP-1-associated adaptor protein Gadkin inhibits ARP2/3 by sequestering it on intracellular vesicles. Consistent with a role of Gadkin in DC physiology, we here report Gadkin expression in bone marrow-derived DCs and show that its protein level and posttranslational modification are regulated upon LPS-induced DC maturation. DCs derived from Gadkin-deficient mice were normal with regards to differentiation and maturation, but displayed increased actin polymerization. While the actin-dependent processes of macropinocytosis and cell spreading were not affected, loss of Gadkin significantly impaired DC migration in vitro, however, in vivo DC migration was unperturbed suggesting the presence of compensatory mechanisms.
Keywords:Actin-Related Protein 2-3 Complex, Actins, Cell Communication, Cell Differentiation, Cell Movement, Dendritic Cells, Immune System Processes, Lymphocyte Activation, Membrane Proteins, Inbred C57BL Mice, T-Lymphocytes, Transcription Factor AP-1, {rho} GTP-Binding Proteins, Animals, Mice
Source:PLoS ONE
ISSN:1932-6203
Publisher:Public Library of Science (U.S.A.)
Volume:10
Number:12
Page Range:e0143883
Date:1 December 2015
Official Publication:https://doi.org/10.1371/journal.pone.0143883
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library