Keshavarz Mozhgan, Smith Quinton
Department of Chemical and Biomolecular Engineering, University of California, Irvine, CA, United States.
Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, CA, United States.
Adv Funct Mater. 2024 Sep 11;34(37). doi: 10.1002/adfm.202402360. Epub 2024 May 14.
Tissue self-assembly relies on the interplay between structural cues imparted by the extracellular matrix and instructive chemical factors that guide cellular signaling pathways. Here, we report that endothelial cell-laden gelatin-based hydrogels with optimized mechanical and chemical properties facilitate vasculogenesis and recruitment of endogenous blood vessels . We demonstrate that these engineered matrices, with tailored viscoelastic features and stiffness, drive vascular self-assembly in a yes-associated protein mechanosensing-dependent manner through αvβ3 integrin and matrix metalloproteinase 2 activity. Our research highlights how the extracellular matrix, in the form of gelatin-based hydrogels with adjustable stress relaxation rates, drive vascular morphogenesis in the absence of growth factor supplementation, lending to a minimalistic platform for discretizing features of the microenvironment niche. Collectively, these results demonstrate a testbed that enables mechanistic evaluation of morphogenetic processes. Specifically, our results show how mechanical cues impact signaling pathways that modulate vascular remodeling, a critical tissue engineering paradigm needed for the translational application of vascularized grafts for regenerative medicine applications.
组织自组装依赖于细胞外基质赋予的结构线索与指导细胞信号通路的指导性化学因子之间的相互作用。在此,我们报告具有优化的机械和化学性质的载有内皮细胞的明胶基水凝胶促进血管生成和内源性血管的募集。我们证明,这些具有定制粘弹性特征和刚度的工程化基质通过αvβ3整合素和基质金属蛋白酶2活性,以一种与Yes相关蛋白机械传感依赖性方式驱动血管自组装。我们的研究突出了以具有可调节应力松弛速率的明胶基水凝胶形式存在的细胞外基质如何在不补充生长因子的情况下驱动血管形态发生,从而为离散微环境生态位特征提供了一个简约平台。总的来说,这些结果展示了一个能够对形态发生过程进行机制评估的试验台。具体而言,我们的结果表明机械线索如何影响调节血管重塑的信号通路,这是用于再生医学应用的血管化移植物转化应用所需的关键组织工程范例。