INSERM U1026, Université Victor Segalen Bordeaux 2, Bordeaux, France.
PLoS One. 2012;7(7):e41163. doi: 10.1371/journal.pone.0041163. Epub 2012 Jul 19.
Angiogenesis, the formation of new blood vessels by sprouting from pre-existing ones, is critical for the establishment and maintenance of complex tissues. Angiogenesis is usually triggered by soluble growth factors such as VEGF. However, geometrical cues also play an important role in this process. Here we report the induction of angiogenesis solely by SVVYGLR peptide micropatterning on polymer surfaces. SVVYGLR peptide stripes were micropatterned onto polymer surfaces by photolithography to study their effects on endothelial cell (EC) behavior. Our results showed that the EC behaviors (cell spreading, orientation and migration) were significantly more guided and regulated on narrower SVVYGLR micropatterns (10 and 50 µm) than on larger stripes (100 µm). Also, EC morphogenesis into tube formation was switched on onto the smaller patterns. We illustrated that the central lumen of tubular structures can be formed by only one-to-four cells due to geometrical constraints on the micropatterns which mediated cell-substrate adhesion and generated a correct maturation of adherens junctions. In addition, sprouting of ECs and vascular networks were also induced by geometrical cues on surfaces micropatterned with SVVYGLR peptides. These micropatterned surfaces provide opportunities for mimicking angiogenesis by peptide modification instead of exogenous growth factors. The organization of ECs into tubular structures and the induction of sprouting angiogenesis are important towards the fabrication of vascularized tissues, and this work has great potential applications in tissue engineering and tissue regeneration.
血管生成是指从预先存在的血管中长出新的血管,对于复杂组织的建立和维持至关重要。血管生成通常是由可溶性生长因子如 VEGF 触发的。然而,几何线索在这个过程中也起着重要的作用。在这里,我们报告了仅通过 SVVYGLR 肽在聚合物表面上的微图案化来诱导血管生成。通过光刻将 SVVYGLR 肽条微图案化到聚合物表面上,以研究它们对内皮细胞 (EC) 行为的影响。我们的结果表明,与较大的条纹 (100 µm) 相比,EC 行为 (细胞铺展、定向和迁移) 在较窄的 SVVYGLR 微图案 (10 和 50 µm) 上受到更明显的引导和调节。此外,EC 形态发生成管状结构也在较小的图案上开启。我们说明,由于微图案对细胞-基底附着的限制以及对黏着连接的正确成熟的影响,管状结构的中央腔室可以仅由一个到四个细胞形成。此外,SVVYGLR 肽微图案化表面上的几何线索也诱导了 EC 和血管网络的发芽。这些微图案化表面为通过肽修饰而不是外源性生长因子模拟血管生成提供了机会。EC 形成管状结构和诱导发芽血管生成对于血管化组织的制造非常重要,这项工作在组织工程和组织再生方面具有很大的应用潜力。