Biology Department, Duke University, Durham, NC 27708, USA.
Sci Signal. 2010 May 4;3(120):ra35. doi: 10.1126/scisignal.2000654.
Cell invasion through basement membranes during development, immune surveillance, and metastasis remains poorly understood. To gain further insight into this key cellular behavior, we performed an in vivo screen for regulators of cell invasion through basement membranes, using the simple model of Caenorhabditis elegans anchor cell invasion, and identified 99 genes that promote invasion, including the genes encoding the chaperonin complex cct. Notably, most of these genes have not been previously implicated in invasive cell behavior. We characterized members of the cct complex and 11 other gene products, determining the distinct aspects of the invasive cascade that they regulate, including formation of a specialized invasive cell membrane and its ability to breach the basement membrane. RNA interference-mediated knockdown of the human orthologs of cct-5 and lit-1, which had not previously been implicated in cell invasion, reduced the invasiveness of metastatic carcinoma cells, suggesting that a conserved genetic program underlies cell invasion. These results increase our understanding of the genetic underpinnings of cell invasion and also provide new potential therapeutic targets to limit this behavior.
细胞通过基底膜的侵袭在发育、免疫监视和转移过程中仍未被充分理解。为了更深入地了解这一关键的细胞行为,我们利用秀丽隐杆线虫锚定细胞侵袭的简单模型,进行了体内筛选,以寻找调节细胞通过基底膜侵袭的调控因子,共鉴定出 99 个促进侵袭的基因,包括编码伴侣蛋白复合物 CCT 的基因。值得注意的是,这些基因中的大多数以前并未被涉及到侵袭细胞行为中。我们对 CCT 复合物和其他 11 个基因产物的成员进行了表征,确定了它们调节的侵袭级联反应的不同方面,包括形成专门的侵袭细胞膜及其穿透基底膜的能力。以前未被认为与细胞侵袭有关的 CCT-5 和 LIT-1 的人类同源物的 RNA 干扰介导的敲低降低了转移性癌细胞的侵袭性,这表明细胞侵袭的背后存在保守的遗传程序。这些结果增加了我们对细胞侵袭遗传基础的理解,也为限制这种行为提供了新的潜在治疗靶点。