Zhang Shanshan, Felthaus Oliver, Prantl Lukas, Ma Nan, Machatschek Rainhard
Institute of Chemistry and Biochemistry, Freie Universität Berlin, Takustrasse 3, 14195 Berlin, Germany.
Helmholtz-Zentrum Hereon, Institute of Active Polymers, Kantstrasse 55, 14513 Teltow, Germany.
PNAS Nexus. 2024 May 21;3(6):pgae202. doi: 10.1093/pnasnexus/pgae202. eCollection 2024 Jun.
To assess cellular behavior within heterogeneous tissues, such as bone, skin, and nerves, scaffolds with biophysical gradients are required to adequately replicate the in vivo interaction between cells and their native microenvironment. In this study, we introduce a strategy for depositing ultrathin films comprised of laminin-111 with precisely controlled biophysical gradients onto planar substrates using the Langmuir-Blodgett (LB) technique. The gradient is created by controlled desynchronization of the barrier compression and substrate withdrawal speed during the LB deposition process. Characterization of the films was performed using techniques such as atomic force microscopy and confocal fluorescence microscopy, enabling the comprehensive analysis of biophysical parameters along the gradient direction. Furthermore, human adipose-derived stem cells were seeded onto the gradient films to investigate the influence of protein density on cell attachment, showing that the distribution of the cells can be modulated by the arrangement of the laminin at the air-water interface. The presented approach not only allowed us to gain insights into the intricate interplay between biophysical cues and cell behavior within complex tissue environments, but it is also suited as a screening approach to determine optimal protein concentrations to achieve a target cellular output.
为了评估异质组织(如骨骼、皮肤和神经)内的细胞行为,需要具有生物物理梯度的支架来充分复制细胞与其天然微环境之间的体内相互作用。在本研究中,我们介绍了一种使用朗缪尔-布洛杰特(LB)技术在平面基板上沉积由层粘连蛋白-111组成且具有精确控制的生物物理梯度的超薄膜的策略。该梯度是通过在LB沉积过程中控制屏障压缩和基板撤回速度的不同步来产生的。使用原子力显微镜和共聚焦荧光显微镜等技术对薄膜进行表征,从而能够沿梯度方向对生物物理参数进行全面分析。此外,将人脂肪来源的干细胞接种到梯度薄膜上,以研究蛋白质密度对细胞附着的影响,结果表明细胞的分布可以通过层粘连蛋白在空气-水界面处的排列来调节。所提出的方法不仅使我们能够深入了解复杂组织环境中生物物理线索与细胞行为之间的复杂相互作用,而且还适合作为一种筛选方法来确定实现目标细胞输出的最佳蛋白质浓度。