Department of Aerospace and Mechanical Engineering, University of Notre Dame, Notre Dame, IN, 46556, USA.
Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN, 46556, USA; Harper Cancer Research Institute, University of Notre Dame, Notre Dame, IN, 46556, USA.
Biomaterials. 2023 Jun;297:122110. doi: 10.1016/j.biomaterials.2023.122110. Epub 2023 Apr 8.
Obesity has been linked with numerous health issues as well as an increased risk of breast cancer. Although effects of direct obesity in patient outcomes is widely studied, effects of exposure to obesity-related systemic influences in utero have been overlooked. In this study, we investigated the effect of multigenerational obesity on epithelial cell migration and invasion using decellularized breast tissues explanted from normal female mouse pups from a diet induced multigenerational obesity mouse model. We first studied the effect of multigenerational diet on the mechanical properties, adipocyte size, and collagen structure of these mouse breast tissues, and then, examined the migration and invasion behavior of normal (KTB-21) and cancerous (MDA-MB-231) human mammary epithelial cells on the decellularized matrices from each diet group. Breast tissues of mice whose dams had been fed with high-fat diet exhibited larger adipocytes and thicker and curvier collagen fibers, but only slightly elevated elastic modulus and inflammatory cytokine levels. MDA-MB-231 cancer cell motility and invasion were significantly greater on the decellularized matrices from mice whose dams were fed with high-fat diet. A similar trend was observed with normal KTB-21 cells. Our results showed that the collagen curvature was the dominating factor on this enhanced motility and stretching the matrices to equalize the collagen fiber linearity of the matrices ameliorated the observed increase in cell migration and invasion in the mice that were exposed to a high-fat diet in utero. Previous studies indicated an increase in serum leptin concentration for those children born to an obese mother. We generated extracellular matrices using primary fibroblasts exposed to various concentrations of leptin. This produced curvier ECM and increased breast cancer cell motility for cells seeded on the decellularized ECM generated with increasing leptin concentration. Our study shows that exposure to obesity in utero is influential in determining the extracellular matrix structure, and that the resultant change in collagen curvature is a critical factor in regulating the migration and invasion of breast cancer cells.
肥胖与许多健康问题有关,并且乳腺癌的风险也会增加。尽管人们广泛研究了肥胖对患者预后的直接影响,但人们忽视了胎儿期暴露于肥胖相关的系统性影响的作用。在这项研究中,我们使用从饮食诱导的多代肥胖小鼠模型中正常雌性小鼠幼仔的去细胞化乳腺组织,研究了多代肥胖对上皮细胞迁移和侵袭的影响。我们首先研究了多代饮食对这些小鼠乳腺组织的机械性能、脂肪细胞大小和胶原结构的影响,然后检查了正常(KTB-21)和癌性(MDA-MB-231)人乳腺上皮细胞在来自每个饮食组的去细胞化基质上的迁移和侵袭行为。其母鼠喂食高脂肪饮食的小鼠的乳腺组织中脂肪细胞较大,胶原纤维较厚且更弯曲,但弹性模量和炎症细胞因子水平仅略有升高。MDA-MB-231 癌细胞在母鼠喂食高脂肪饮食的小鼠的去细胞化基质上的迁移和侵袭能力明显更强。在正常的 KTB-21 细胞中也观察到类似的趋势。我们的结果表明,胶原曲率是这种增强的运动性的主要因素,拉伸基质以均等化基质中的胶原纤维线性度可以改善在胎儿期暴露于高脂肪饮食的小鼠中观察到的细胞迁移和侵袭增加。先前的研究表明,肥胖母亲所生的孩子血清瘦素浓度增加。我们使用暴露于各种浓度瘦素的原代成纤维细胞生成细胞外基质。这产生了更弯曲的 ECM,并增加了在随瘦素浓度增加而生成的去细胞化 ECM 上接种的乳腺癌细胞的迁移能力。我们的研究表明,胎儿期暴露于肥胖会影响细胞外基质结构,并且胶原曲率的变化是调节乳腺癌细胞迁移和侵袭的关键因素。