Center for Interdisciplinary Research in Biology (CIRB), College de France, CNRS UMR7241, INSERM U1050, PSL Research University, Paris, France; Sorbonne Université, Collège doctoral, Paris, France.
Université de Paris, UR2496 Pathologies, Imagerie et Biothérapies Orofaciales et Plateforme Imagerie du Vivant, Paris, France; AP-HP, Services Odontologie, (GH Paris Est, Paris Nord, Henri Mondor), France.
Biomaterials. 2021 Jan;268:120594. doi: 10.1016/j.biomaterials.2020.120594. Epub 2020 Dec 19.
Blood perfusion of grafted tissue constructs is a hindrance to the success of stem cell-based therapies by limiting cell survival and tissue regeneration. Implantation of a pre-vascularized network engineered in vitro has thus emerged as a promising strategy for promoting blood supply deep into the construct, relying on inosculation with the host vasculature. We aimed to fabricate in vitro tissue constructs with mature microvascular networks, displaying perivascular recruitment and basement membrane, taking advantage of the angiogenic properties of dental pulp stem cells and self-assembly of endothelial cells into capillaries. Using digital scanned light-sheet microscopy, we characterized the generation of dense microvascular networks in collagen hydrogels and established parameters for quantification of perivascular recruitment. We also performed original time-lapse analysis of stem cell recruitment. These experiments demonstrated that perivascular recruitment of dental pulp stem cells is driven by PDGF-BB. Recruited stem cells participated in deposition of vascular basement membrane and vessel maturation. Mature microvascular networks thus generated were then compared to those lacking perivascular coverage generated using stem cell conditioned medium. Implantation in athymic nude mice demonstrated that in vitro maturation of microvascular networks improved blood perfusion and cell survival within the construct. Taken together, these data demonstrate the strong potential of in vitro production of mature microvasculature for improving cell-based therapies.
移植组织构建物的血液灌注会限制细胞存活和组织再生,从而成为干细胞治疗成功的障碍。因此,体外构建预血管化网络已成为促进构建物深部血液供应的一种有前途的策略,该策略依赖于与宿主脉管系统的吻合。我们旨在利用牙髓干细胞的血管生成特性和内皮细胞自我组装成毛细血管的特性,制造具有成熟微血管网络的体外组织构建物,显示出血管周募集和基底膜。利用数字扫描光片显微镜,我们描述了在胶原水凝胶中密集微血管网络的生成,并建立了用于量化血管周募集的参数。我们还对干细胞募集进行了原始的延时分析。这些实验表明,牙髓干细胞的血管周募集是由 PDGF-BB 驱动的。募集的干细胞参与了血管基底膜的沉积和血管成熟。然后将生成的成熟微血管网络与使用干细胞条件培养基生成的缺乏血管周覆盖的网络进行比较。在无胸腺裸鼠中的植入实验表明,体外微血管网络的成熟改善了构建物内的血液灌注和细胞存活。总之,这些数据表明体外产生成熟微血管对于改善基于细胞的治疗具有巨大潜力。