Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
F. M. Kirby Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Cell Stem Cell. 2021 Jan 7;28(1):63-78.e7. doi: 10.1016/j.stem.2020.09.012. Epub 2020 Oct 13.
Enormous amounts of essential intracellular events are crowdedly packed inside picoliter-sized cellular space. However, the significance of the physical properties of cells remains underappreciated because of a lack of evidence of how they affect cellular functionalities. Here, we show that volumetric compression regulates the growth of intestinal organoids by modifying intracellular crowding and elevating Wnt/β-catenin signaling. Intracellular crowding varies upon stimulation by different types of extracellular physical/mechanical cues and leads to significant enhancement of Wnt/β-catenin signaling by stabilizing the LRP6 signalosome. By enhancing intracellular crowding using osmotic and mechanical compression, we show that expansion of intestinal organoids was facilitated through elevated Wnt/β-catenin signaling and greater intestinal stem cell (ISC) self-renewal. Our results provide an entry point for understanding how intracellular crowdedness functions as a physical regulator linking extracellular physical cues with intracellular signaling and potentially facilitate the design of engineering approaches for expansion of stem cells and organoids.
大量重要的细胞内事件被拥挤地压缩在皮升级别的细胞空间内。然而,由于缺乏关于它们如何影响细胞功能的证据,细胞的物理性质的重要性仍然未被充分认识。在这里,我们表明体积压缩通过改变细胞内拥挤程度和提高 Wnt/β-连环蛋白信号来调节肠类器官的生长。细胞内拥挤程度因不同类型的细胞外物理/机械线索的刺激而变化,并通过稳定 LRP6 信号体来显著增强 Wnt/β-连环蛋白信号。通过使用渗透压和机械压缩来增强细胞内拥挤程度,我们表明通过提高 Wnt/β-连环蛋白信号和增加肠干细胞(ISC)自我更新,促进了肠类器官的扩张。我们的结果为理解细胞内拥挤程度如何作为一种物理调节剂,将细胞外物理线索与细胞内信号联系起来提供了一个切入点,并可能有助于设计用于扩展干细胞和类器官的工程方法。