The non-redundant role of N-WASP in podosome-mediated matrix degradation in macrophages
Autor: | Athanassios Dovas, Dianne Cox, Leora M. Nusblat |
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Rok vydání: | 2011 |
Předmět: |
Histology
Podosome macromolecular substances Matrix metalloproteinase Matrix (biology) Biology Transfection Article Pathology and Forensic Medicine Mice Animals Humans Macrophage Cytoskeleton Actin Metalloproteinase Macrophages fungi Cell Biology General Medicine Cell biology Cytoskeletal Proteins Haematopoiesis RNA silencing Cell Surface Extensions Wiskott-Aldrich Syndrome Protein |
Zdroj: | European Journal of Cell Biology. 90:205-212 |
ISSN: | 0171-9335 |
DOI: | 10.1016/j.ejcb.2010.07.012 |
Popis: | Wiskott-Aldrich Syndrome Protein (WASP) is a hematopoietic cell-specific regulator of Arp2/3-dependent actin polymerization. Despite the presence of the highly homologous N-WASP (neural-WASP), macrophages from WAS patients are devoid of podosomes, adhesion structures in cells of the monocytic lineage capable of matrix degradation via matrix metalloproteases (MMPs), suggesting that WASP and N-WASP play unique roles in macrophages. To determine whether N-WASP also plays a unique role in macrophage function, N-WASP expression was reduced using silencing RNA in a sub-line of RAW 264.7 macrophages (RAW/LR5). Similar to reduction in WASP levels, cells with reduced N-WASP levels were rounder and less polarized. Interestingly, podosomes still formed when N-WASP was reduced but they were unable to perform matrix degradation. This defect was rescued by re-expression of N-WASP, but not by over-expression of WASP, indicating that these proteins play distinct roles in podosome function. Additionally, reducing N-WASP levels mistargets the metalloprotease MT1-MMP and it no longer localizes to podosomes. However, N-WASP was only found to co-localize with MT1-MMP positive vesicles at podosomes, suggesting that N-WASP may play a role on the targeting or fusion of MMP-containing vesicles to podosomes in macrophage-like cells. |
Databáze: | OpenAIRE |
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