Microtubule-dependent formation of podosomal adhesion structures in primary human macrophages

• Published in: Journal of cell science Vol. 113 Pt 23; no. 23; pp. 4165 - 4176
• Main Authors: Linder, S, Hüfner, K, Wintergerst, U, Aepfelbacher, M
• Format: Journal Article
• Language: English
• Published: England 01.12.2000
• Subjects: Actin Cytoskeleton - metabolism; Actins - analysis; Antineoplastic Agents - pharmacology; Cell Adhesion - drug effects; Cell Adhesion - physiology; Focal Adhesions - drug effects; Focal Adhesions - metabolism; Humans; Macrophages - chemistry; Macrophages - physiology; Macrophages - ultrastructure; Microinjections; Microtubule-Associated Proteins - metabolism; Microtubules - metabolism; Minor Histocompatibility Antigens; Mutagenesis - physiology; Nocodazole - pharmacology; Oligopeptides - metabolism; Oligopeptides - pharmacology; Peptide Fragments - metabolism; Peptide Fragments - pharmacology; Protein Structure, Tertiary; Protein-Tyrosine Kinases; Proteins - chemistry; Proteins - metabolism; Proteins - pharmacology; Proto-Oncogene Proteins - chemistry; Proto-Oncogene Proteins - genetics; src Homology Domains - genetics; Tubulin - analysis; Vinculin - analysis; Wiskott-Aldrich Syndrome Protein
• ISSN: 0021-9533; 1477-9137
• DOI: 10.1242/jcs.113.23.4165

Podosomes are unique actin-rich adhesion structures of monocyte-derived cells such as macrophages and osteoclasts. They clearly differ from other substratum-contacting organelles like focal adhesions in morphological and functional regards. Formation of podosomes has been shown to be dependent on the small GTPase CDC42Hs and its effector Wiskott-Aldrich syndrome protein (WASp). In this study, we investigated the functional relation between podosomes and the microtubule system in primary human macrophages. We demonstrate that, in contrast to focal adhesions, assembly of podosomes in macrophages and their monocytic precursors is dependent on an intact microtubule system. In contrast, experiments using Wiskott-Aldrich syndrome (WAS) macrophages indicate that the microtubule system is not reciprocally dependent on podosomes. A potential linker between podosomes and microtubules may be WASp itself, considering that microinjection of the WASp polyproline domain prevents podosome reassembly. This polyproline domain is thought to link WASp to microtubules via CDC42 interacting protein 4 (CIP4). Consistently, macrophages microinjected with CIP4 constructs deficient in either the microtubule- or the WASp-binding domain also fail to reassemble podosomes. In sum, our findings show that microtubules are essential for podosome formation in primary human macrophages and that WASp and CIP4 may be involved in this phenomenon.