Podosomes and invadopodia: tools to breach vascular basement membrane

References

• Beaty BT, Sharma VP, Bravo-Cordero JJ, Simpson MA, Eddy RJ, Koleske AJ, Condeelis J. beta1 integrin regulates Arg to promote invadopodial maturation and matrix degradation. Mol Biol Cell 2013; 24:1661–75, S1-11; http://dx.doi.org/10.1091/mbc.E12-12-0908
   PubMed Web of Science ®Google Scholar
• Murphy DA, Courtneidge SA. The 'ins' and 'outs' of podosomes and invadopodia: characteristics, formation and function. Nat Rev Mol Cell Biol 2011; 12:413–26; PMID:21697900; http://dx.doi.org/10.1038/nrm3141
   PubMed Web of Science ®Google Scholar
• Carman CV, Sage PT, Sciuto TE, de la Fuente MA, Geha RS, Ochs HD, Dvorak HF, Dvorak AM, Springer TA. Transcellular diapedesis is initiated by invasive podosomes. Immunity 2007; 26:784–97; PMID:17570692; http://dx.doi.org/10.1016/j.immuni.2007.04.015
   PubMed Web of Science ®Google Scholar
• Friedl P, Alexander S. Cancer invasion and the microenvironment: plasticity and reciprocity. Cell 2011; 147:992–1009; PMID:22118458; http://dx.doi.org/10.1016/j.cell.2011.11.016
   PubMed Web of Science ®Google Scholar
• Hallmann R, Horn N, Selg M, Wendler O, Pausch F, Sorokin LM. Expression and function of laminins in the embryonic and mature vasculature. Physiol Rev 2005; 85:979–1000; PMID:15987800; http://dx.doi.org/10.1152/physrev.00014.2004
   PubMed Web of Science ®Google Scholar
• Yurchenco PD, Ruben GC. Basement membrane structure in situ: evidence for lateral associations in the type IV collagen network. JCell Biol 1987; 105:2559–68; PMID:3693393; http://dx.doi.org/10.1083/jcb.105.6.2559
   PubMed Web of Science ®Google Scholar
• Glentis A, Gurchenkov V, Matic Vignjevic D. Assembly, heterogeneity, and breaching of the basement membranes. Cell Adh Migr 2014; 8:236–45; PMID:24727304; http://dx.doi.org/10.4161/cam.28733
   PubMed Web of Science ®Google Scholar
• Kelley LC, Lohmer LL, Hagedorn EJ, Sherwood DR. Traversing the basement membrane in vivo: a diversity of strategies. J Cell Biol 2014; 204:291–302; PMID:24493586; http://dx.doi.org/10.1083/jcb.201311112
   PubMed Web of Science ®Google Scholar
• Leong HS, Robertson AE, Stoletov K, Leith SJ, Chin CA, Chien AE, Hague MN, Ablack A, Carmine-Simmen K, McPherson VA, et al. Invadopodia are required for cancer cell extravasation and are a therapeutic target for metastasis. Cell Rep 2014; 8:1558–70; PMID:25176655; http://dx.doi.org/10.1016/j.celrep.2014.07.050
   PubMed Web of Science ®Google Scholar
• Seano G, Chiaverina G, Gagliardi PA, di Blasio L, Puliafito A, Bouvard C, Sessa R, Tarone G, Sorokin L, Helley D, et al. Endothelial podosome rosettes regulate vascular branching in tumour angiogenesis. Nat Cell Biol 2014; 16:931–41, 1–8; http://dx.doi.org/10.1038/ncb3036
   PubMed Web of Science ®Google Scholar
• Tarone G, Cirillo D, Giancotti FG, Comoglio PM, Marchisio PC. Rous sarcoma virus-transformed fibroblasts adhere primarily at discrete protrusions of the ventral membrane called podosomes. Exp Cell Res 1985; 159:141–57; PMID:2411576; http://dx.doi.org/10.1016/S0014-4827(85)80044-6
   PubMed Web of Science ®Google Scholar
• Caligaris-Cappio F, Bergui L, Tesio L, Corbascio G, Tousco F, Marchisio PC. Cytoskeleton organization is aberrantly rearranged in the cells of B chronic lymphocytic leukemia and hairy cell leukemia. Blood 1986; 67:233–9; PMID:3484425
   PubMed Web of Science ®Google Scholar
• Block MR, Badowski C, Millon-Fremillon A, Bouvard D, Bouin AP, Faurobert E, Gerber-Scokaert D, Planus E, Albiges-Rizo C. Podosome-type adhesions and focal adhesions, so alike yet so different. Eur J Cell Biol 2008; 87:491–506; PMID:18417250; http://dx.doi.org/10.1016/j.ejcb.2008.02.012
   PubMed Web of Science ®Google Scholar
• Branch KM, Hoshino D, Weaver AM. Adhesion rings surround invadopodia and promote maturation. Biol Open 2012; 1:711–22; PMID:23213464; http://dx.doi.org/10.1242/bio.20121867
   PubMed Web of Science ®Google Scholar
• Buccione R, Orth JD, McNiven MA. Foot and mouth: podosomes, invadopodia and circular dorsal ruffles. Nat Rev Mol Cell Biol 2004; 5:647–57; PMID:15366708; http://dx.doi.org/10.1038/nrm1436
   PubMed Web of Science ®Google Scholar
• Moreau V, Tatin F, Varon C, Genot E. Actin can reorganize into podosomes in aortic endothelial cells, a process controlled by Cdc42 and RhoA. Mol Cell Biol 2003; 23:6809–22; PMID:12972601; http://dx.doi.org/10.1128/MCB.23.19.6809-6822.2003
   PubMed Web of Science ®Google Scholar
• Osiak AE, Zenner G, Linder S. Subconfluent endothelial cells form podosomes downstream of cytokine and RhoGTPase signaling. Exp Cell Res 2005; 307:342–53; PMID:15894313; http://dx.doi.org/10.1016/j.yexcr.2005.03.035
   PubMed Web of Science ®Google Scholar
• Juin A, Planus E, Guillemot F, Horakova P, Albiges-Rizo C, Genot E, Rosenbaum J, Moreau V, Saltel F. Extracellular matrix rigidity controls podosome induction in microvascular endothelial cells. Biol Cell 2013; 105:46–57; PMID:23106484; http://dx.doi.org/10.1111/boc.201200037
   PubMed Web of Science ®Google Scholar
• Varon C, Tatin F, Moreau V, Van Obberghen-Schilling E, Fernandez-Sauze S, Reuzeau E, Kramer I, Genot E. Transforming growth factor beta induces rosettes of podosomes in primary aortic endothelial cells. Mol Cel Biol 2006; 26:3582–94; PMID:16611998; http://dx.doi.org/10.1128/MCB.26.9.3582-3594.2006
   PubMed Web of Science ®Google Scholar
• Linder S, Nelson D, Weiss M, Aepfelbacher M. Wiskott-Aldrich syndrome protein regulates podosomes in primary human macrophages. Proc Natl Acad Sci U S A 1999; 96:9648–53; PMID:10449748; http://dx.doi.org/10.1073/pnas.96.17.9648
   PubMed Web of Science ®Google Scholar
• Guegan F, Tatin F, Leste-Lasserre T, Drutel G, Genot E, Moreau V. p190B RhoGAP regulates endothelial-cell-associated proteolysis through MT1-MMP and MMP2. J Cell Sci 2008; 121:2054–61; PMID:18505793; http://dx.doi.org/10.1242/jcs.025817
   PubMed Web of Science ®Google Scholar
• Wang J, Taba Y, Pang J, Yin G, Yan C, Berk BC. GIT1 mediates VEGF-induced podosome formation in endothelial cells: critical role for PLCgamma. Arterioscler Thromb Vasc Biol 2009; 29:202–8; PMID:19023093; http://dx.doi.org/10.1161/ATVBAHA.108.174391
   PubMed Web of Science ®Google Scholar
• Rottiers P, Saltel F, Daubon T, Chaigne-Delalande B, Tridon V, Billottet C, Reuzeau E, Genot E. TGFbeta-induced endothelial podosomes mediate basement membrane collagen degradation in arterial vessels. J Cell Sci 2009; 122:4311–8; PMID:19887587; http://dx.doi.org/10.1242/jcs.057448
   PubMed Web of Science ®Google Scholar
• Primo L, Seano G, Roca C, Maione F, Gagliardi PA, Sessa R, Martinelli M, Giraudo E, di Blasio L, Bussolino F. Increased expression of alpha6 integrin in endothelial cells unveils a proangiogenic role for basement membrane. Cancer Res 2010; 70:5759–69; PMID:20570893; http://dx.doi.org/10.1158/0008-5472.CAN-10-0507
   PubMed Web of Science ®Google Scholar
• Gligorijevic B, Wyckoff J, Yamaguchi H, Wang Y, Roussos ET, Condeelis J. N-WASP-mediated invadopodium formation is involved in intravasation and lung metastasis of mammary tumors. J Cell Sci 2012; 125:724–34; PMID:22389406; http://dx.doi.org/10.1242/jcs.092726
   PubMed Web of Science ®Google Scholar
• Beaty BT, Wang Y, Bravo-Cordero JJ, Sharma VP, Miskolci V, Hodgson L, Condeelis J. Talin regulates moesin-NHE-1 recruitment to invadopodia and promotes mammary tumor metastasis. J Cell Biol 2014; 205:737–51; PMID:24891603; http://dx.doi.org/10.1083/jcb.201312046
   PubMed Web of Science ®Google Scholar
• Hagedorn EJ, Yashiro H, Ziel JW, Ihara S, Wang Z, Sherwood DR. Integrin acts upstream of netrin signaling to regulate formation of the anchor cell's invasive membrane in C. elegans. Dev Cell 2009; 17:187–98; PMID:19686680; http://dx.doi.org/10.1016/j.devcel.2009.06.006
   PubMed Web of Science ®Google Scholar