creases

  • 文章类型: Journal Article
    深深蚀刻的前额折痕表明老化。各种治疗方法,如填充剂注射,脂肪移植,整容手术用于移除它们。然而,缺乏与皮下组织变化相关的解剖结构的知识和浅层肌肉腱膜系统,对适当的治疗没有共识。我们已经研究了涉及前额皱折的皮下结构;这将有助于建立改善治疗的选择标准。获得了五个未固定的成年亚洲尸体的前额部分。从骨膜中取出含有前额皱褶的组织,并使用粗略观察进行检查,射线照相术,组织学,和纳米计算机断层扫描。所有方法都显示皮肤折痕区域的真皮,即从身体表面可见的褶皱,通过脂肪隔片之间的三维纤维结构与额肌结合。该结构在皮肤褶皱附近致密,在其他区域稀疏而薄。特别是,它紧紧地绑在折痕下面的真皮上,胶原纤维穿过表皮。此外,折痕附近的皮肤附件比正常区域少,或者它们完全缺失;表皮较厚,真皮乳头更发达。据认为,真皮-额肌之间的纤维脂肪间隔结构的密度和坚固性以及紧接在折痕下方的表皮和真皮的特定结构是特征性的塑料前额折痕。
    Deeply etched forehead creases indicate aging. Various treatments such as filler injections, fat grafting, and facelift surgery are used to remove them. However, knowledge of the anatomical structures associated with subcutaneous tissue changes and the superficial musculoaponeurotic system is lacking, and there is no consensus about the appropriate treatment. We have investigated the subcutaneous structures involved in forehead creases; this will help to establish selection criteria for improved treatment. The forehead sections of five unfixed adult Asian cadavers were obtained. Tissues containing forehead creases were removed from the periosteum and were examined using gross observation, radiography, histology, and nano-computed tomography. All methods revealed that the dermis in the skin crease area, namely the fold visible from the body surface, was bound to the frontalis muscle by a three-dimensional fibrous structure between the fatty septa. This structure was dense near the skin folds and sparse and thin in other areas. In particular, it was tightly bound to the dermis immediately below the crease, with collagen fibers traversing toward the epidermis. In addition, there were fewer skin appendages near the crease than in the normal area, or they were absent altogether; the epidermis was thicker, and the dermal papillae were more developed. It is thought that the density and firmness of the fibrous fatty septal structures between the dermis-frontalis muscle and the specific structures of the epidermis and dermis immediately below the crease account for the characteristic plastic forehead creases.
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  • 文章类型: Journal Article
    This work combines experiments and finite element simulations to study the effect of pre-imposed cyclic loading on surface instability of silicon rubber under compression. We first fabricate cuboid blocks of silicon rubber and pinch them cyclicly a few times. Then, an in-house apparatus is set to apply uniaxial compression on the silicon rubber under exact plane strain conditions. Surprisingly, we find multiple creases on the surface of silicone rubber, significantly different from what have been observed on the samples without the cyclic pinching. To reveal the underlying physics for these experimentally observed multiple creases, we perform detailed nanoindentation experiments to measure the material properties at different locations of the silicon rubber. The modulus is found to be nonuniform and varies along the thickness direction after the cyclic pinching. According to these experimental results, three-layer and multilayer finite element models are built with different materials properties informed by experiments. The three-layer finite element model can excellently explain the nucleation and pattern of multiple surface creases on the surface of compressed silicone rubber, in good agreement with experiments. Counterintuitively, the multilayer model with gradient modulus cannot be used to explain the multiple creases observed in our experiments. According to these simulations, the experimentally observed multiple creases should be attributed to a thin and stiff layer formed on the surface of silicon rubber after the pre-imposed cyclic loading.
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  • 文章类型: Journal Article
    尽管其微环境具有独特的功能和生化差异,但分支形态发生的结构特征在各种器官和物种之间仍具有出色的可重复性。驱动分支形态发生的调节网络采用细胞产生的和被动的机械力,将来自微环境的细胞外信号整合到形态发生运动中。细胞产生的力在局部起作用以重塑细胞外基质(ECM)并控制相邻细胞之间的相互作用。被动机械力是原位机械不稳定性的产物,其触发相邻组织的平面外屈曲和裂开变形。屈曲和裂开形态发生背后的许多分子和物理信号仍不清楚,需要发现新的实验策略。这里,我们突出的软材料系统,已被设计为显示可编程的扣和折痕。使用合成材料对屈曲和裂开形态发生的物理化学和时空特征进行建模,可能有助于我们理解驱动不同器官和物种分支形态发生的物理机制。
    The architectural features of branching morphogenesis demonstrate exquisite reproducibility among various organs and species despite the unique functionality and biochemical differences of their microenvironment. The regulatory networks that drive branching morphogenesis employ cell-generated and passive mechanical forces, which integrate extracellular signals from the microenvironment into morphogenetic movements. Cell-generated forces function locally to remodel the extracellular matrix (ECM) and control interactions among neighboring cells. Passive mechanical forces are the product of in situ mechanical instabilities that trigger out-of-plane buckling and clefting deformations of adjacent tissues. Many of the molecular and physical signals that underlie buckling and clefting morphogenesis remain unclear and require new experimental strategies to be uncovered. Here, we highlight soft material systems that have been engineered to display programmable buckles and creases. Using synthetic materials to model physicochemical and spatiotemporal features of buckling and clefting morphogenesis might facilitate our understanding of the physical mechanisms that drive branching morphogenesis across different organs and species.
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