Department of Cancer Biology, Vanderbilt University Medical Center, 2220 Pierce Avenue, Nashville, TN 37232-6840, USA.
J Cell Sci. 2013 Jul 15;126(Pt 14):2979-89. doi: 10.1242/jcs.079475. Epub 2013 Jul 10.
Remodeling of extracellular matrix (ECM) is a fundamental cell property that allows cells to alter their microenvironment and move through tissues. Invadopodia and podosomes are subcellular actin-rich structures that are specialized for matrix degradation and are formed by cancer and normal cells, respectively. Although initial studies focused on defining the core machinery of these two structures, recent studies have identified inputs from both growth factor and adhesion signaling as crucial for invasive activity. This Commentary will outline the current knowledge on the upstream signaling inputs to invadopodia and podosomes and their role in governing distinct stages of these invasive structures. We discuss invadopodia and podosomes as adhesion structures and highlight new data showing that invadopodia-associated adhesion rings promote the maturation of already-formed invadopodia. We present a model in which growth factor stimulation leads to phosphoinositide 3-kinase (PI3K) activity and formation of invadopodia, whereas adhesion signaling promotes exocytosis of proteinases at invadopodia.
细胞外基质 (ECM) 的重塑是细胞的基本特性之一,使细胞能够改变其微环境并在组织中移动。侵袭伪足和足突是细胞内富含肌动蛋白的亚细胞结构,分别专门用于基质降解,并由癌细胞和正常细胞形成。尽管最初的研究集中于定义这两种结构的核心机制,但最近的研究表明,生长因子和黏附信号的输入对于侵袭活性至关重要。本评论将概述侵袭伪足和足突的上游信号输入及其在调节这些侵袭结构不同阶段中的作用的最新知识。我们将侵袭伪足和足突视为黏附结构,并强调新的数据表明,与侵袭伪足相关的黏附环促进已经形成的侵袭伪足的成熟。我们提出了一个模型,其中生长因子刺激导致磷酸肌醇 3-激酶 (PI3K) 活性和侵袭伪足的形成,而黏附信号促进蛋白酶在侵袭伪足处的胞吐作用。