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Soft matrix is a natural stimulator for cellular invasiveness

机译:软基质是细胞侵袭性的天然刺激物

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Directional mesenchymal cell invasion in vivo is understood to be a stimulated event and to be regulated by cytokines, chemokines, and types of extracellular matrix (ECM). Instead, by focusing on the cellular response to ECM stiffness, we found that soft ECM (low stiffness) itself is sufficient to prevent stable cell-to-cell adherens junction formation, up-regulate matrix metalloproteinase (MMP) secretion, promote MMP activity, and induce invadosome-like protrusion (ILP) formation. Consistently, similar ILP formation was also detected in a three-dimensional directional invasion assay in soft matrix. Primary human fibroblasts spontaneously form ILPs in a very narrow range of ECM stiffness (0.1-0.4 kPa), and such ILP formation is Src family kinase dependent. In contrast, spontaneous ILP formation in malignant cancer cells and fibrosarcoma cells occurs across a much wider range of ECM stiffness, and these tumor cell ILPs are also more prominent at lower stiffness. These findings suggest that ECM softness is a natural stimulator for cellular invasiveness.
机译:体内定向间充质细胞的入侵被认为是一种刺激事件,并受细胞因子,趋化因子和细胞外基质(ECM)类型的调节。相反,通过关注细胞对ECM硬度的反应,我们发现柔软的ECM(低硬度)本身足以防止稳定的细胞间粘附连接形成,上调基质金属蛋白酶(MMP)分泌,促进MMP活性,并诱导成卵泡状突起(ILP)形成。一致地,在软基质中的三维定向浸润试验中也检测到类似的ILP形成。初级人类成纤维细胞在很窄的ECM硬度(0.1-0.4 kPa)范围内自发形成ILP,并且这种ILP形成是Src家族激酶依赖性的。相比之下,恶性癌细胞和纤维肉瘤细胞中的自发性ILP形成跨ECM硬度的范围更广,而这些肿瘤细胞ILP在较低的硬度下也更为突出。这些发现表明ECM的柔软性是细胞侵袭性的天然刺激物。

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