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层粘连蛋白5可促进皮肤等效模型中致密板层的组装。

Laminin 5 can promote assembly of the lamina densa in the skin equivalent model.

作者信息

Tsunenaga M, Adachi E, Amano S, Burgeson R E, Nishiyama T

机构信息

Shiseido Life Science Research Center, Yokohama, Japan.

出版信息

Matrix Biol. 1998 Dec;17(8-9):603-13. doi: 10.1016/s0945-053x(98)90111-1.

DOI:10.1016/s0945-053x(98)90111-1
PMID:9923653
Abstract

Skin equivalents were prepared by culturing human keratinocytes on the surface of type I collagen gel contracted by human skin fibroblasts (dermal equivalents) and by raising the gel to an air-liquid interface. A stratified squamous epithelium was formed with a well-differentiated cornified layer at the top of keratinocyte layers within 7 days after plating of the keratinocytes on the dermal equivalents. Although major basement membrane components such as collagens IV and VII and laminin 5 were detected immunohistochemically at the dermal-epidermal junction, a lamina densa was rarely observed by electron microscopy even in 14-day skin equivalents. When laminin 5 (1, 5 or 20 microg/ml) was added to the culture medium on day 7 through day 14, types IV and VII collagens at the dermal-epidermal junction stained more strongly by immunohistochemistry compared with the control. Patches of lamina densa were present along the epidermal-dermal junction, and vesicles containing electron-opaque sheets approximately 0.6 microm in diameter that reacted with anti-collagen IV antibody were also observed in basal keratinocytes in 14-day skin equivalents by electron microscopy. Morphometric analysis showed that the total length of lamina densa along the dermal-epidermal junction as well as in the vesicles increased up to 180%, 230% or 520% of control cultures by the addition of laminin 5 (1, 5 or 20 microg/ml, respectively). These results suggest that laminin 5 accelerates formation of the lamina densa along the dermal-epidermal junction of the skin equivalents, depending on the concentration of laminin 5 supplemented exogenously.

摘要

通过在由人皮肤成纤维细胞收缩的I型胶原凝胶表面培养人角质形成细胞(真皮替代物)并将凝胶提升至气液界面来制备皮肤替代物。在将角质形成细胞接种到真皮替代物上7天内,形成了分层的鳞状上皮,在角质形成细胞层顶部有分化良好的角质层。尽管免疫组织化学检测到在真皮-表皮交界处存在主要的基底膜成分,如IV型和VII型胶原以及层粘连蛋白5,但即使在培养14天的皮肤替代物中,电子显微镜下也很少观察到致密层。当在第7天至第14天向培养基中添加层粘连蛋白5(1、5或20微克/毫升)时,与对照组相比,真皮-表皮交界处的IV型和VII型胶原免疫组织化学染色更强。在表皮-真皮交界处存在致密层斑块,并且在培养14天的皮肤替代物的基底角质形成细胞中,通过电子显微镜还观察到含有直径约0.6微米的电子不透明片层的囊泡,这些囊泡与抗IV型胶原抗体发生反应。形态计量分析表明,通过添加层粘连蛋白5(分别为1、5或20微克/毫升),沿真皮-表皮交界处以及囊泡中的致密层总长度增加至对照培养物的180%、230%或520%。这些结果表明,层粘连蛋白5根据外源补充的层粘连蛋白5的浓度,加速皮肤替代物真皮-表皮交界处致密层的形成。

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