Biophysics Program, Stanford University, Stanford, CA 94305, USA.
Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
Biomaterials. 2017 Mar;121:179-192. doi: 10.1016/j.biomaterials.2016.12.005. Epub 2016 Dec 9.
The physical properties of the extracellular matrix play an essential role in guiding stem cell differentiation and tissue morphogenesis both in vivo and in vitro. Existing work to investigate the role of matrix mechanics in directing stem cell proliferation, self-renewal, and differentiation has been limited by the poor attachment and survival of human pluripotent cells cultured on soft matrices (Young's modulus E ≲ 1000 Pa). To address this limitation we developed a protocol for generating semi-interpenetrating networks of polyacrylamide and recombinant basement membrane. Using these materials, we found that human embryonic stem cells (hESCs) remained proliferative and pluripotent even when grown in small colonies and on surfaces ranging in stiffness from 150 to 12000 Pa, spanning the range of tissue stiffnesses likely to be encountered in the embryo. Considerable recent attention has focused on the role of the transcriptional coactivator and Hippo effector YAP in regulating differentiation and cell proliferation both in the early embryo and in vitro. We found that while YAP localized to the nucleus on substrates of E ≳ 1000 Pa, its localization was heterogeneous on substrates of moduli ≲ 450 Pa, with predominantly nuclear localization at the colony periphery and mixed cytoplasmic and nuclear localization for cells in the colony interior, a pattern reminiscent of YAP subcellular localization in the inner cell mass (ICM) of the early embryo. In addition, hESC colony dynamics were highly responsive to substrate stiffness, with cells assembling into monolayers, multilayer structures, and transient, hollow rosettes in response to decreasing substrate stiffnesses in the range of 12000 to 150 Pa. We suggest that soft, ligand-rich substrates such as are described here provide a promising means of recapitulating aspects of early mammalian development that are otherwise inaccessible, and more broadly may be useful in the derivation of complex tissues from pluripotent cells in an in vitro setting.
细胞外基质的物理性质在体内和体外指导干细胞分化和组织形态发生中起着至关重要的作用。现有的研究基质力学在指导干细胞增殖、自我更新和分化中的作用的工作受到限制,因为在软基质上培养的人类多能细胞附着和存活不良(杨氏模量 E ≲ 1000 Pa)。为了解决这一限制,我们开发了一种聚丙酰胺和重组基底膜的半互穿网络生成方案。使用这些材料,我们发现人类胚胎干细胞(hESC)即使在小菌落中生长并且在从 150 到 12000 Pa 的硬度范围内的表面上生长时,也保持增殖和多能性,这涵盖了胚胎中可能遇到的组织硬度范围。最近人们相当关注转录共激活因子和 Hippo 效应因子 YAP 在调节早期胚胎和体外分化和细胞增殖中的作用。我们发现,当 YAP 在杨氏模量 E ≥ 1000 Pa 的基质上定位于核内时,其在模量 ≲ 450 Pa 的基质上的定位是异质的,在菌落边缘主要是核内定位,而在菌落内部的细胞中则是细胞质和核内定位混合,这种模式类似于早期胚胎内细胞团(ICM)中 YAP 的亚细胞定位。此外,hESC 菌落动力学对基质硬度高度敏感,细胞在杨氏模量从 12000 到 150 Pa 的范围内响应基质硬度的降低而组装成单层、多层结构和短暂的空心玫瑰花结。我们认为,像这里描述的那样柔软、配体丰富的基质为再现早期哺乳动物发育的某些方面提供了有希望的手段,这些方面在其他情况下是无法获得的,更广泛地说,在体外从多能细胞中衍生复杂组织时可能是有用的。