3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga, Guimarães, Portugal; CÚRAM SFI Research Centre for Medical Devices, National University of Ireland, Galway, Ireland.
3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga, Guimarães, Portugal.
Biomater Adv. 2022 Feb;133:112611. doi: 10.1016/j.msec.2021.112611. Epub 2021 Dec 22.
The simultaneous generation of multiple tissues and their functional assembly into complex tissues remains a critical challenge for regenerative medicine. The tissue-to-tissue interface connecting two adjacent tissues is vital in effective tissue function. The presented worked hypothesize that differential functional property can be engineered by modulating the macromolecular composition of a 3D hydrogel construct and distinctively endow stem cell fate. Hence, it was possible to successfully generate macromolecular constructs by using the extracellular matrix (ECM)-based materials; type I collagen (Col I) and hyaluronic acid (HA); and natural-derived biomaterials as methacrylated gellan-gum (GGMA). The 3D hydrogel constructs consisted of two dissimilar layers: 1) Col I: HA hydrogel and 2) GGMA hydrogel. The tissue-to-tissue interface was created by seeding human mesenchymal stem cells (MSCs) between the two layers. Differential functional rheological and mechanical properties characterized the acellular 3D gradient hydrogel constructs. The cell-based 3D hydrogel constructs were assessed for MSCs viability by live/dead staining. Assessing apoptosis by flow cytometry, data showed the feasibility of the 3D hydrogel constructs in maintaining cell viability with no apoptosis induction onto MSCs. A homogeneous distribution was achieved in a successful cellular tissue-to-tissue interface. Human MSCs low proliferative rate and low ECM deposition were seen for all constructs; however, lower proliferative rate within the ECM microenvironment highlights controlled self-renewal of MSCs. The 3D hydrogel constructs maintained the human MSCs phenotype, yet the macromolecular modulation allowed tuning the human MSCs morphology from round to spindle-shaped phenotype. The intrinsic properties of the 3D cell-based hydrogel construct induced differential inflammatory and angiogenic paracrine secretory profiles owing to the dissimilar engineered biophysical milieu. Human MSCs sense the nearby macromolecular environment adjusting the cell-ECM interactions, which influence cell behaviour and fate. Beyond multi-tissue regeneration, the engineered cellular 3D hydrogel constructs may simultaneously address immune regeneration.
同时生成多种组织并将其功能组装成复杂组织仍然是再生医学的一个关键挑战。连接两个相邻组织的组织-组织界面对于有效组织功能至关重要。本研究假设可以通过调节 3D 水凝胶构建体的大分子组成并赋予干细胞命运独特的特性来实现差异化的功能特性。因此,有可能通过使用基于细胞外基质(ECM)的材料;I 型胶原(Col I)和透明质酸(HA);以及天然衍生的生物材料,成功地生成大分子构建体,如甲基丙烯酰化凝胶多糖(GGMA)。3D 水凝胶构建体由两层组成:1)Col I:HA 水凝胶和 2)GGMA 水凝胶。通过在两层之间接种人间充质干细胞(MSCs)来创建组织-组织界面。无细胞 3D 梯度水凝胶构建体的特征在于差异功能流变学和机械性能。通过活/死染色评估基于细胞的 3D 水凝胶构建体中 MSC 的活力。通过流式细胞术评估细胞凋亡,数据表明 3D 水凝胶构建体在不诱导 MSC 凋亡的情况下维持细胞活力的可行性。在成功的细胞组织-组织界面中实现了均匀分布。所有构建体中均观察到人 MSCs 增殖率低和细胞外基质沉积低;然而,在 ECM 微环境中,增殖率较低突出了 MSC 的受控自我更新。3D 水凝胶构建体保持了人 MSCs 的表型,而大分子调节允许将人 MSCs 的形态从圆形调整为纺锤形表型。3D 基于细胞的水凝胶构建体的固有特性由于不同的工程生物物理环境而诱导了差异化的炎症和血管生成旁分泌分泌谱。人 MSCs 感知附近的大分子环境,调整细胞-细胞外基质相互作用,从而影响细胞行为和命运。除了多组织再生外,工程化的细胞 3D 水凝胶构建体还可以同时解决免疫再生问题。