Hirose R, Kligman L H
Department of Dermatology, University of Pennsylvania School of Medicine, Philadelphia.
J Invest Dermatol. 1988 May;90(5):697-702. doi: 10.1111/1523-1747.ep12560912.
Ultrastructural visualization of mouse elastic fibers has been hampered by the small size and sparseness of the fibers. Furthermore, with conventional uranyl acetate and lead citrate stains, the elastin matrix remains electron-lucent so that even severe elastosis is elusive. The addition of tannic acid to the staining procedure renders the elastin matrix extremely electron dense and easily located even at low scanning power. Microfibrils, as with conventional stains, are electron-dense and clearly visible. This study describes, with the aid of tannic acid, normal hairless mouse elastic fibers and their progressive degeneration with increasing exposure to ultraviolet radiation. Results with the two staining methods are contrasted. In addition, photodamaged mouse and human elastic fibers are compared for differences and similarities.
小鼠弹性纤维的超微结构可视化一直受到纤维尺寸小和分布稀疏的阻碍。此外,使用传统的醋酸铀和柠檬酸铅染色时,弹性蛋白基质在电子显微镜下仍呈透明状,因此即使是严重的弹性组织变性也难以察觉。在染色过程中加入单宁酸可使弹性蛋白基质具有极高的电子密度,即使在低扫描功率下也能轻松定位。与传统染色一样,微原纤维电子密度高且清晰可见。本研究借助单宁酸描述了正常无毛小鼠的弹性纤维及其在紫外线照射增加时的渐进性退化。对比了两种染色方法的结果。此外,还比较了光损伤的小鼠和人类弹性纤维的异同。