Karlinski Zur Maayan, Bhattacharya Bidisha, Solomonov Inna, Ben Dror Sivan, Savidor Alon, Levin Yishai, Prior Amir, Sapir Tamar, Harris Talia, Olender Tsviya, Schmidt Rita, Schwarz J M, Sagi Irit, Buxboim Amnon, Reiner Orly
Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
Department of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot, Israel.
Nat Commun. 2025 May 1;16(1):4094. doi: 10.1038/s41467-025-59252-w.
The viscoelastic properties of tissues influence their morphology and cellular behavior, yet little is known about changes in these properties during brain malformations. Lissencephaly, a severe cortical malformation caused by LIS1 mutations, results in a smooth cortex. Here, we show that human-derived brain organoids with LIS1 mutation exhibit increased stiffness compared to controls at multiple developmental stages. This stiffening correlates with abnormal extracellular matrix (ECM) expression and organization, as well as elevated water content, measured by diffusion-weighted MRI. Short-term MMP9 treatment reduces both stiffness and water diffusion levels to control values. Additionally, a computational microstructure mechanical model predicts mechanical changes based on ECM organization. These findings suggest that LIS1 plays a critical role in ECM regulation during brain development and that its mutation leads to significant viscoelastic alterations.
组织的粘弹性特性会影响其形态和细胞行为,但对于脑畸形过程中这些特性的变化却知之甚少。无脑回畸形是一种由LIS1突变引起的严重皮质畸形,会导致皮质表面平滑。在此,我们表明,与对照组相比,携带LIS1突变的人源脑类器官在多个发育阶段都表现出硬度增加。这种硬度增加与细胞外基质(ECM)的异常表达和组织以及通过扩散加权磁共振成像测量的含水量升高相关。短期MMP9处理可将硬度和水扩散水平降低至对照值。此外,一个计算微观结构力学模型可根据ECM组织预测力学变化。这些发现表明,LIS1在脑发育过程中的ECM调节中起关键作用,其突变会导致显著的粘弹性改变。