Baude Jane A, Li Megan D, Jackson Sabrina M, Sharma Abhishek, Walter Daniella I, Stowers Ryan S
University of California, Santa Barbara, Department of Molecular, Cellular, and Developmental Biology.
University of California, Santa Barbara, Department of Mechanical Engineering.
bioRxiv. 2025 Mar 3:2025.02.28.640825. doi: 10.1101/2025.02.28.640825.
Reconstituted basement membrane (rBM) products like Matrigel are widely used in 3D culture models of epithelial tissues and cancer. However, their utility is hindered by key limitations, including batch variability, xenogenic contaminants, and a lack of tunability. To address these challenges, we engineered a 3D basement membrane (eBM) matrix by conjugating defined extracellular matrix (ECM) adhesion peptides (IKVAV, YIGSR, RGD) to an alginate hydrogel network with precisely tunable stiffness and viscoelasticity. We optimized the mechanical and biochemical properties of the engineered basement membranes (eBMs) to support mammary acinar morphogenesis in MCF10A cells, similar to rBM. We found that IKVAV-modified, fast-relaxing (τ1 = 30-150 s), and soft (E = 200 Pa) eBMs best promoted polarized acinar structures. Clusters became invasive and lost polarity only when the IKVAV-modified eBM exhibited both similar stiffness to a malignant breast tumor (E = 4000 Pa) and slow stress relaxation (τ1 = 600-1100 s). Notably, tumor-like stiffness alone was not sufficient to drive invasion in fast stress relaxing matrices modified with IKVAV. In contrast, RGD-modified matrices promoted a malignant phenotype regardless of mechanical properties. We also utilized this system to interrogate the mechanism driving acinar and tumorigenic phenotypes in response to microenvironmental parameters. A balance in activity between β1- and β4-integrins was observed in the context of IKVAV-modified eBMs, prompting further investigation into the downstream mechanisms. We found differences in hemidesmosome formation and production of endogenous laminin in response to peptide type, stress relaxation, and stiffness. We also saw that inhibiting either focal adhesion kinase or hemidesmosome signaling in IKVAV eBMs prevented acinus formation. This eBM matrix is a powerful, reductionist, xenogenic-free system, offering a robust platform for both fundamental research and translational applications in tissue engineering and disease modeling.
像基质胶这样的重组基底膜(rBM)产品被广泛应用于上皮组织和癌症的三维培养模型中。然而,它们的效用受到关键限制的阻碍,包括批次变异性、异种污染物以及缺乏可调性。为了应对这些挑战,我们通过将特定的细胞外基质(ECM)黏附肽(IKVAV、YIGSR、RGD)与具有精确可调刚度和粘弹性的藻酸盐水凝胶网络结合,设计了一种三维基底膜(eBM)基质。我们优化了工程化基底膜(eBM)的力学和生化特性,以支持MCF10A细胞中的乳腺腺泡形态发生,类似于rBM。我们发现,IKVAV修饰的、快速松弛(τ1 = 30 - 150秒)且柔软(E = 200帕)的eBM最能促进极化腺泡结构的形成。只有当IKVAV修饰的eBM表现出与恶性乳腺肿瘤相似的刚度(E = 4000帕)和缓慢的应力松弛(τ1 = 600 - 1100秒)时,细胞簇才会变得具有侵袭性并失去极性。值得注意的是,仅肿瘤样刚度不足以驱动IKVAV修饰的快速应力松弛基质中的侵袭。相比之下,无论力学性能如何,RGD修饰的基质都会促进恶性表型。我们还利用这个系统来探究响应微环境参数驱动腺泡和致瘤表型的机制。在IKVAV修饰的eBM背景下,观察到β1 - 和β4 - 整合素之间的活性平衡,这促使我们进一步研究下游机制。我们发现,响应肽类型、应力松弛和刚度,半桥粒形成和内源性层粘连蛋白产生存在差异。我们还发现,在IKVAV eBM中抑制粘着斑激酶或半桥粒信号传导会阻止腺泡形成。这种eBM基质是一个强大的、简化的、无异种的系统,为组织工程和疾病建模的基础研究和转化应用提供了一个强大的平台。