Department of Cell Biology, Faculty of Science, Charles University in Prague, Prague, Czech Republic.
Eur J Cell Biol. 2010 Sep;89(9):674-80. doi: 10.1016/j.ejcb.2010.04.003.
Invadopodia and podosomes have been intensively studied because of their involvement in the degradation of extracellular matrix. As both structures have been studied mostly on thin matrices, their commonly reported shapes and characteristics may differ from those in vivo. To assess the morphology of invadopodia in a complex 3D environment, we observed invadopodial formation in cells grown on a dense matrix based on cell-free dermis. We have found that invadopodia differ in morphology when cells grown on the dermis-based matrix and thin substrates are compared. The cells grown on the dermis-based matrix display invadopodia which are formed by a thick protruding base rich in F-actin, phospho-paxillin, phospho-cortactin and phosphotyrosine signal, from which numerous thin filaments protrude into the matrix. The protruding filaments are composed of an F-actin core and are free of phospho-paxillin and phospho-cortactin but capped by phosphotyrosine signal. Furthermore, we found that a matrix-degrading activity is localized to the base of invadopodia and not along the matrix-penetrating protrusions. Our description of invadopodial structures on a dermis-based matrix should greatly aid the development of new criteria for the identification of invadopodia in vivo, and opens up the possibility of studying the invadopodia-related signaling in a more physiological environment.
侵袭伪足和足突被深入研究,因为它们参与细胞外基质的降解。由于这两种结构主要在薄基质上进行研究,因此它们通常报道的形状和特征可能与体内不同。为了评估在复杂的 3D 环境中侵袭伪足的形态,我们观察了在基于无细胞真皮的密集基质上生长的细胞中侵袭伪足的形成。我们发现,与在薄底物上生长的细胞相比,在基于真皮基质上生长的细胞中的侵袭伪足在形态上存在差异。在基于真皮基质的基质上生长的细胞显示出侵袭伪足,这些伪足由富含 F-肌动蛋白、磷酸化黏着斑蛋白、磷酸化桩蛋白和磷酸化酪氨酸信号的厚突出基底形成,从该基底中突出许多细纤维进入基质。突出的纤维由 F-肌动蛋白核心组成,不含磷酸化黏着斑蛋白和磷酸化桩蛋白,但被磷酸化酪氨酸信号帽盖。此外,我们发现基质降解活性定位于侵袭伪足的基底,而不是沿基质穿透的突起。我们对基于真皮基质的侵袭伪足结构的描述将极大地帮助开发体内侵袭伪足鉴定的新标准,并为在更生理的环境中研究侵袭伪足相关信号提供了可能性。