Spuul Pirjo, Ciufici Paolo, Veillat Véronique, Leclercq Anne, Daubon Thomas, Kramer IJsbrand, Génot Elisabeth
Université de Bordeaux; Bordeaux, France; INSERM U1045; Bordeaux, France; IECB; European Institute of Chemistry and Biology; Pessac, France.
Small GTPases. 2014;5:e28195. doi: 10.4161/sgtp.28713. Epub 2014 May 8.
Podosomes and invadopodia (collectively known as invadosomes) are specialized plasma-membrane actin-based microdomains that combine adhesive properties with matrix degrading and/or mechanosensor activities. These organelles have been extensively studied in vitro and current concerted efforts aim at establishing their physiological relevance and subsequent association with human diseases. Proper functioning of the bone, immune, and vascular systems is likely to depend on these structures while their occurrence in cancer cells appears to be linked to tumor metastasis. The elucidation of the mechanisms driving invadosome assembly is a prerequisite to understanding their role in vivo and ultimately to controlling their functions. Adhesive and soluble ligands act via transmembrane receptors that propagate signals to the cytoskeleton via small G proteins of the Rho family, assisted by tyrosine kinases and scaffold proteins to induce invadosome formation and rearrangements. Oncogene expression and cell-cell interactions may also trigger their assembly. Manipulation of the signals that regulate invadosome formation and dynamics could therefore be a strategy to interfere with their functions in a multitude of pathological settings, such as excessive bone breakdown, infections, vascular remodeling, transendothelial diapedesis, and metastasis.
小体和侵袭性伪足(统称为侵袭体)是基于肌动蛋白的特殊质膜微结构域,它们将黏附特性与基质降解和/或机械传感活性结合在一起。这些细胞器已在体外得到广泛研究,目前的协同努力旨在确定它们的生理相关性以及随后与人类疾病的关联。骨骼、免疫和血管系统的正常功能可能依赖于这些结构,而它们在癌细胞中的出现似乎与肿瘤转移有关。阐明驱动侵袭体组装的机制是理解它们在体内的作用并最终控制其功能的先决条件。黏附性和可溶性配体通过跨膜受体起作用,这些受体通过Rho家族的小G蛋白将信号传递到细胞骨架,在酪氨酸激酶和支架蛋白的协助下诱导侵袭体形成和重排。癌基因表达和细胞间相互作用也可能触发它们的组装。因此,操纵调节侵袭体形成和动态的信号可能是一种策略,可在多种病理情况下干扰它们的功能,如过度的骨质破坏、感染、血管重塑、跨内皮细胞渗出和转移。