Department of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, OR, USA.
Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
FEBS J. 2018 Jan;285(1):8-27. doi: 10.1111/febs.14123. Epub 2017 Jun 22.
Invadopodia and podosomes are discrete, actin-based molecular protrusions that form in cancer cells and normal cells, respectively, in response to diverse signaling pathways and extracellular matrix cues. Although they participate in a host of different cellular processes, they share a common functional theme of controlling pericellular proteolytic activity, which sets them apart from other structures that function in migration and adhesion, including focal adhesions, lamellipodia, and filopodia. In this review, we highlight research that explores the function of these complex structures, including roles for podosomes in embryonic and postnatal development, in angiogenesis and remodeling of the vasculature, in maturation of the postsynaptic membrane, in antigen sampling and recognition, and in cell-cell fusion mechanisms, as well as the involvement of invadopodia at multiple steps of the metastatic cascade, and how all of this may apply in the treatment of human disease states. Finally, we explore recent research that implicates a novel role for exosomes and microvesicles in invadopodia-dependent and invadopodia-independent mechanisms of invasion, respectively.
侵袭伪足和足突是离散的、基于肌动蛋白的分子突起,分别在癌细胞和正常细胞中形成,以响应不同的信号通路和细胞外基质线索。尽管它们参与了许多不同的细胞过程,但它们具有共同的功能主题,即控制细胞周围的蛋白水解活性,这使它们有别于其他在迁移和黏附中起作用的结构,包括黏附斑、片状伪足和丝状伪足。在这篇综述中,我们强调了探索这些复杂结构功能的研究,包括足突在胚胎和出生后发育、血管生成和血管重塑、突触后膜成熟、抗原采样和识别以及细胞-细胞融合机制中的作用,以及侵袭伪足在转移级联的多个步骤中的参与,以及所有这些如何适用于人类疾病状态的治疗。最后,我们探讨了最近的研究,这些研究暗示了外泌体和微泡在侵袭伪足依赖性和非依赖性侵袭机制中的新作用。