用蛋白酶消化扫描声学显微镜评价衰老、糖尿病和皮肤伤口。

Pathobiology of aging & age related diseases Pub Date : 2018-09-06 eCollection Date: 2018-01-01 DOI:10.1080/20010001.2018.1516072
Katsutoshi Miura, Kanna Yamashita
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引用次数: 9

摘要

扫描声学显微镜(SAM)可以通过计算声音通过组织的速度来评估组织的刚度。SOS随着组织刚度的增加而增加。对蛋白酶消化的敏感性取决于蛋白质的类型、浓度和修饰。我们分析了福尔马林固定石蜡包埋皮肤切片的SOS图像,这些皮肤切片来自老年人、年轻人、糖尿病患者和非糖尿病患者,以及慢性和急性伤口。SAM提供与LM相似的高分辨率组织学,并在胃蛋白酶治疗后显示特征性的SOS改变。老年受试者(尤其是女性)真皮样本的SOS值低于年轻人,这表明与年龄相关的皮肤软化和松动。老年女性的SOS值低于年轻女性和老年男性。真皮SOS与表皮厚度呈正相关。老年人表皮SOS值高于青壮年,蛋白酶消化后0.5h呈快速下降趋势。糖尿病患者网状真皮比非糖尿病患者表现出更大的胃蛋白酶抵抗。慢性创伤比急性创伤表现出更高的SOS值和胃蛋白酶抵抗。SOS随衰老、糖尿病和伤口纤维化的变化反映了与衰老和病程相关的组织学和力学变化。表皮厚度反映了皮肤硬度与年龄相关的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of aging, diabetes mellitus, and skin wounds by scanning acoustic microscopy with protease digestion.

Evaluation of aging, diabetes mellitus, and skin wounds by scanning acoustic microscopy with protease digestion.

Evaluation of aging, diabetes mellitus, and skin wounds by scanning acoustic microscopy with protease digestion.

Evaluation of aging, diabetes mellitus, and skin wounds by scanning acoustic microscopy with protease digestion.

Scanning acoustic microscopy (SAM) can assess tissue stiffness by calculating the speed of sound (SOS) through tissues. SOS increases as tissue stiffness increases. Sensitivity to protease digestion depends on protein type, concentration, and modification. We analyzed the SOS images of formalin-fixed paraffin-embedded skin sections from elderly, young, diabetic, and nondiabetic subjects, as well as chronic and acute wounds. SAM provided high-resolution histology similar to LM and revealed characteristic SOS alteration following pepsin treatment. SOS values of dermis samples from elderly subjects (especially females) were lower than those of younger adults, which was indicative of age-related dermal softening and loosening. SOS values of elderly females were lower than those of younger females and elderly males. Dermal SOS showed a positive correlation with epidermal thickness. SOS values of epidermis of elderly subjects were higher than those of younger adults and showed a rapid decline 0.5h after protease digestion. Reticular dermis of diabetic patients exhibited greater pepsin resistance than that of nondiabetic patients. Chronic wounds exhibited greater SOS values and pepsin resistance than acute wounds. SOS variation with aging, diabetes mellitus, and wound fibrosis reflected histological and mechanical changes associated with senescence and disease duration. Epidermal thickness reflects age-related changes in dermal stiffness.

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