Institute for Mechanical Systems, Department of Mechanical and Process Engineering, ETH Zürich, 8092 Zürich, Switzerland.
Institute of Molecular Health Sciences, Department of Biology, ETH Zürich, 8093 Zürich, Switzerland.
Acta Biomater. 2024 Sep 15;186:316-329. doi: 10.1016/j.actbio.2024.07.013. Epub 2024 Jul 14.
Aging leads to biochemical and biomechanical changes in skin, with biological and functional consequences. Despite extensive literature on skin aging, there is a lack of studies which investigate the maturation of the tissue and connect the microscopic changes in the skin to its macroscopic biomechanical behavior as it evolves over time. The present work addresses this knowledge gap using multiscale characterization of skin in a murine model considering newborn, adult and aged mice. Monotonic uniaxial loading, tension relaxation with change of bath, and loading to failure tests were performed on murine skin samples from different age groups, complemented by inflation experiments and atomic force microscopy indentation measurements. In parallel, skin samples were characterized using histological and biochemical techniques to assess tissue morphology, collagen organization, as well as collagen content and cross-linking. We show that 1-week-old skin differs across nearly all measured parameters from adult skin, showing reduced strain stiffening and tensile strength, a thinner dermis, lower collagen content and altered crosslinking patterns. Surprisingly, adult and aged skin were similar across most biomechanical parameters in the physiologic loading range, while aged skin had lower tensile strength and lower stiffening behavior at large force values. This correlates with altered collagen content and cross-links. Based on a computational model, differences in mechanocoupled stimuli in the skin of the different age groups were calculated, pointing to a potential biological significance of the age-induced biomechanical changes in regulating the local biophysical environment of dermal cells. STATEMENT OF SIGNIFICANCE: Skin microstructure and the emerging mechanical properties change with age, leading to biological, functional and health-related consequences. Despite extensive literature on skin aging, only very limited quantitative data are available on microstructural changes and the corresponding macroscopic biomechanical behavior as they evolve over time. This work provides a wide-range multiscale mechanical characterization of skin of newborn, adult and aged mice, and quantifies microstructural correlations in tissue morphology, collagen content, organization and cross-linking. Remarkably, aged skin retained normal hydration and normal biomechanical function in the physiological loading range but showed significantly reduced properties at super-physiological loading. Our data show that age-related microstructural differences have a profound effect not only on tissue-level properties but also on the cell-level biophysical environment.
衰老是皮肤生物化学和生物力学变化的原因,具有生物学和功能方面的影响。尽管有大量关于皮肤衰老的文献,但缺乏研究将组织的成熟与皮肤随时间推移的微观变化与其宏观生物力学行为联系起来。本工作通过在新生、成年和老年小鼠的模型中对皮肤进行多尺度表征来解决这一知识空白。对来自不同年龄组的小鼠皮肤样本进行了单调单轴加载、改变浴槽时的张力松弛和失效加载测试,同时进行了膨胀实验和原子力显微镜压痕测量。平行地,使用组织学和生化技术对皮肤样本进行了表征,以评估组织形态、胶原组织以及胶原含量和交联。我们表明,1 周龄的皮肤在几乎所有测量参数上都与成年皮肤不同,表现为应变硬化和拉伸强度降低、真皮变薄、胶原含量降低和交联模式改变。令人惊讶的是,在生理负荷范围内,成年和老年皮肤在大多数生物力学参数上相似,而老年皮肤在大力值下的拉伸强度和软化行为较低。这与胶原含量和交联的改变有关。基于计算模型,计算了不同年龄组皮肤中的机械耦合刺激差异,指出了年龄引起的生物力学变化在调节真皮细胞局部生物物理环境方面的潜在生物学意义。
皮肤的微观结构和新出现的机械性能随年龄而变化,导致生物学、功能和健康相关的后果。尽管有大量关于皮肤衰老的文献,但关于微观结构变化及其随时间演变的相应宏观生物力学行为,只有非常有限的定量数据。本工作提供了新生、成年和老年小鼠皮肤的广泛多尺度机械特性表征,并定量了组织形态、胶原含量、组织和交联的微观结构相关性。值得注意的是,老年皮肤在生理负荷范围内保持正常的水合作用和正常的生物力学功能,但在超生理负荷下表现出明显降低的特性。我们的数据表明,与年龄相关的微观结构差异不仅对组织水平的特性,而且对细胞水平的生物物理环境都有深远的影响。