Artym Vira V, Yamada Kenneth M, Mueller Susette C
LCDB/NIDCR, National Institutes of Health, Bethesda, MD 20892, USA.
Methods Mol Biol. 2009;522:211-9. doi: 10.1007/978-1-59745-413-1_15.
Proteolytic degradation of extracellular matrix (ECM) is a critical step during cell invasion and tissue transmigration that is required for many physiological and pathological processes. Cellular structures that mediate cell adhesion to, degradation of, and invasion into ECM are invadopodia of transformed and tumor cells and podosomes of normal monocytic, endothelial, and smooth muscle cells. Detecting the ability of the cell to form invadopodia and podosomes and to degrade ECM is required for studying the invasive capability of the cell. We have developed approximately 50 nm thick fluorescent gelatin matrices that provide a rapid, sensitive, and reliable in vitro system for detection of invadopodia and podosomes, and measurements of the extent of ECM degradation. In this chapter, we provide a detailed protocol for preparation of thin fluorescent gelatin matrices and for evaluation of the results from this degradation assay.
细胞外基质(ECM)的蛋白水解降解是细胞侵袭和组织迁移过程中的关键步骤,许多生理和病理过程都需要这一步骤。介导细胞黏附于ECM、降解ECM并侵入ECM的细胞结构是转化细胞和肿瘤细胞的侵袭性伪足以及正常单核细胞、内皮细胞和平滑肌细胞的足体。检测细胞形成侵袭性伪足和足体以及降解ECM的能力是研究细胞侵袭能力所必需的。我们开发了约50纳米厚的荧光明胶基质,为检测侵袭性伪足和足体以及测量ECM降解程度提供了一种快速、灵敏且可靠的体外系统。在本章中,我们提供了制备薄荧光明胶基质以及评估该降解实验结果的详细方案。