What are invadopodia?2018-02-06T10:43:03+00:00

What are invadopodia?

Invadopodia are actin-rich structures that are present at the basal surfaces of cells that are capable of crossing extracellular barriers, such as cancer cells. The primary function of invadopodia appears to be the focal degradation of the extracellular matrix (ECM) through the secretion of matrix metalloproteinases (MMPs) [1][2]. The formation and function of invadopodia can be described over defined steps that include initiation, extension, ECM degradation and disassembly.

Invadopodia vs Podosomes

Although invadopodia are similar to podosomes in many respects and share many common protein constituents, there are several key differences between these organelles [3]:

  • Invadopodia are found in cancer cells with high metastatic potential, whilst podosomes are generally present in blood cells of myeloid and monocytic lineages.
  • Invadopodia are elongated ventral projections that extend into the underlying ECM, whereas podosomes are rarely seen to project into the matrix.
  • Invadopodia are few in number, approximately between 1 to 10 per cell, whilst podosome numbers can range between 10 to several hundred depending upon the cell type.
  • Invadopodia have a longer lifetime and have been observed to persist for over 8 hours [4], whilst podosomes generally have short half lives, lasting only a couple of minutes in an actively migrating cell.
  • Invadopodia degrade the ECM with a much greater efficiency than podosomes.

Invadopodia composition

The basic structure of an invadopodium consists of a F-actin core similar to that found in podosomes. Microtubules and intermediate filaments have also been detected in mature invadopodia [5]. Actin filament nucleators and their regulators such as the Arp2/3 complex, N-WASP (neuronal Wiskott-Aldrich syndrome protein), WASP-interacting protein (WIP) and cortactin [3] are also found localized to this structure. In addition to the podosome-like structure at their base, invadopodia contain a substantial number of actin filaments arranged as parallel bundles, akin to those observed in filopodia. Cross-linking proteins such as fascin are abundant in invadopodia, and indeed there is a strong correlation between cancer cell invasive potential and fascin expression ([4], as reviewed in [6]).

invadopodium-structure

Schematic depicting the structure of an invadopodia

Importantly, invadopodia also lack the well established multimeric protein complex that encircles the podosomal actin core [7]. It is well established that a ring of integrins are present in podosomes and mediate adhesion with the ECM. In recent years as podosomes and invadopodia have begun to be identified as similar but nonetheless distinct structures. For example, despite being prominent in podosomes, few studies have shown integrins to be associated with invadopodia or play a role in integrin-dependent adhesion in the function of invadopodia [8].

Invadopodia function

Unlike podosomes which can be found in cells under normal physiological conditions, invadopodia are found only in pathological states, most commonly in invasive cancer cells. To this end, invadopodia serve to enhance tumor metastasis by inducing basement membrane disruption through local matrix degradation [9]. To achieve this, the targeted release of surface-exposed proteases (including MMPs) is required [10]. Invadopodia mark the first steps of tumor cell invasion [11].

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References

  1. Gimona M, and Buccione R. Adhesions that mediate invasion. Int. J. Biochem. Cell Biol. 2006; 38(11):1875-92. [PMID: 16790362]
  2. Ayala I, Baldassarre M, Caldieri G, and Buccione R. Invadopodia: a guided tour. Eur. J. Cell Biol. 2005; 85(3-4):159-64. [PMID: 16546558]
  3. Linder S. The matrix corroded: podosomes and invadopodia in extracellular matrix degradation. Trends Cell Biol. 2007; 17(3):107-17. [PMID: 17275303]
  4. Li A, Dawson JC, Forero-Vargas M, Spence HJ, Yu X, König I, Anderson K, and Machesky LM. The actin-bundling protein fascin stabilizes actin in invadopodia and potentiates protrusive invasion. Curr. Biol. 2010; 20(4):339-45. [PMID: 20137952]
  5. Schoumacher M, Goldman RD, Louvard D, and Vignjevic DM. Actin, microtubules, and vimentin intermediate filaments cooperate for elongation of invadopodia. J. Cell Biol. 2010; 189(3):541-56. [PMID: 20421424]
  6. Machesky LM, and Li A. Fascin: Invasive filopodia promoting metastasis. Commun Integr Biol 2010; 3(3):263-70. [PMID: 20714410]
  7. Weaver AM. Invadopodia. Curr. Biol. 2008; 18(9):R362-4. [PMID: 18460310]
  8. Linder S, Wiesner C, and Himmel M. Degrading devices: invadosomes in proteolytic cell invasion. Annu. Rev. Cell Dev. Biol. 2011; 27:185-211. [PMID: 21801014]
  9. Weaver AM. Invadopodia: specialized cell structures for cancer invasion. Clin. Exp. Metastasis 2006; 23(2):97-105. [PMID: 16830222]
  10. Basbaum CB, and Werb Z. Focalized proteolysis: spatial and temporal regulation of extracellular matrix degradation at the cell surface. Curr. Opin. Cell Biol. 1996; 8(5):731-8. [PMID: 8939664]
  11. Gimona M, Buccione R, Courtneidge SA, and Linder S. Assembly and biological role of podosomes and invadopodia. Curr. Opin. Cell Biol. 2008; 20(2):235-41. [PMID: 18337078]