Noblesse E, Nizard C, Cario-André M, Lepreux S, Pain C, Schnebert S, Taïeb A, Kurfurst R
LVMH Recherche, Branche Parfums et Cosmétiques, Saint Jean de Braye, France.
Skin Pharmacol Physiol. 2006;19(2):95-100. doi: 10.1159/000091976. Epub 2006 May 9.
Senile lentigo is a common component of photoaged skin. It is characterized by hyperpigmented macules which affect chronically irradiated skin mostly after the age of 50. This study was undertaken to assess the morphology of senile lentigo on the dorsum of the hands. A systematic comparison between lesional and perilesional skin using histology and transmission electron microscopy was done to determine whether melanocytes or keratinocytes are affected in the evolution of lesions and which tissue structure is modified. The histology study showed that lesional skin is characterized by a hyperpigmented basal layer and an elongation of the rete ridges, which seem to drive deeply into the dermis. The epidermis contained clusters of keratinocytes, which retained and accumulated the melanin pigment. Electron microscopy studies showed important modifications in the lesional skin ultrastructure in comparison with perilesional skin. In melanocytes from perilesional and lesional skin, we observed normal size melanosomes at all stages of maturation in the cytoplasm and in migration within dendrites. No pigment accumulation was observed. However, the morphology of melanocytes in lesional skin revealed an activated status with numerous mitochondria and a well-developed endoplasmic reticulum, which could reflect intense protein synthesis. In basal keratinocytes from lesional skin, we observed numerous melanosome complexes called polymelanosomes, which formed massive caps on the nuclei. Observations in colored semi-thin sections also revealed perturbed structures in the basal layer region, which could explain the skin perturbation. Indeed, we observed keratinocytes that presented important microinvaginations and pendulum melanocytes, which sank into the dermis, beneath the basal layer of keratinocytes. These cell modifications seemed to be due to a perturbation of the dermal-epidermal junction, which appeared disorganized and disrupted and could directly disturb the basal support of the cells.
老年性雀斑是光老化皮肤的常见组成部分。其特征为色素沉着斑,主要影响50岁以后长期受照射的皮肤。本研究旨在评估手部背部老年性雀斑的形态。通过组织学和透射电子显微镜对病损皮肤和病损周围皮肤进行系统比较,以确定在病损演变过程中黑素细胞或角质形成细胞是否受到影响以及哪种组织结构发生了改变。组织学研究表明,病损皮肤的特征是基底层色素沉着增加和 rete 嵴伸长,rete 嵴似乎深深伸入真皮。表皮含有角质形成细胞簇,这些细胞保留并积累了黑色素。电子显微镜研究显示,与病损周围皮肤相比,病损皮肤的超微结构有重要改变。在病损周围皮肤和病损皮肤的黑素细胞中,我们观察到细胞质中各个成熟阶段的黑素体大小正常,且在树突内迁移。未观察到色素积累。然而,病损皮肤中黑素细胞的形态显示其处于激活状态,有大量线粒体和发达的内质网,这可能反映了强烈的蛋白质合成。在病损皮肤的基底角质形成细胞中,我们观察到许多称为多黑素体的黑素体复合物,它们在细胞核上形成了巨大的帽状物。彩色半薄切片的观察还揭示了基底层区域结构紊乱,这可以解释皮肤的紊乱。实际上,我们观察到角质形成细胞出现重要的微内陷和摆动的黑素细胞,这些黑素细胞沉入角质形成细胞基底层下方的真皮中。这些细胞改变似乎是由于真皮 - 表皮连接的紊乱,其看起来杂乱无章且遭到破坏,可能直接干扰了细胞的基底支持。