Demarchez M, Hartmann D J, Regnier M, Asselineau D
CIRD Galderma, Valbonne, France.
Transplantation. 1992 Aug;54(2):317-26. doi: 10.1097/00007890-199208000-00023.
The vascularization and the dermal remodeling of two different types of human skin reconstructed "in vitro" and grafted onto the nude mouse were studied. They were composed of human keratinocytes grown either on a human acellular deepidermized dermis (DED), or on a lattice composed of human fibroblasts embedded in bovine type I collagen, a living dermal equivalent (LDE). At different stages after grafting, the transplants were harvested and processed for an immunohistological study with species-specific and non-species-specific antibodies. At one month after grafting, the two types of grafted dermis contained blood vessels whose vascular basement membranes were labeled with a mouse-specific anti-type IV collagen antibody. With an antibody specific for human type IV collagen, a constant labeling of the vascular basement membrane was only observed in the LDE containing fibroblasts. In the DED, a constant association of the mouse endothelial cells with human type IV collagen was observed at early stages after grafting. At later stages, the human type IV collagen progressively disappeared. On the other hand, the dermal-epidermal junction underneath the human epidermis contained human type IV collagen in the two types of reconstructed skin. Labeling with the species-specific antibodies directed against human or murine type I collagen showed that the ratio murine type I collagen versus human type I collagen increased with time, suggesting that the DED is progressively invaded by mouse fibroblasts that produce the mouse collagen. On the other hand, in the LDE, the preexisting bovine type I collagen became progressively undetectable while both human type I collagen and elastic fibers were deposited by numerous human fibroblasts. Mouse type I collagen was not detected. Altogether, these observations made by grafting human skin reconstructed "in vitro" onto the nude mouse should be interesting for evaluating the usefulness of grafting a dermal substrate together with the epidermal sheet in the treatment of burns.
研究了两种不同类型的“体外”重建并移植到裸鼠身上的人皮肤的血管化和真皮重塑。它们由生长在人脱细胞深层真皮(DED)上或由嵌入牛I型胶原中的人成纤维细胞组成的网格(一种活性真皮替代物,LDE)上的人角质形成细胞构成。在移植后的不同阶段,收获移植组织并用种属特异性和非种属特异性抗体进行免疫组织学研究。移植后一个月,两种移植真皮中都有血管,其血管基底膜用小鼠特异性抗IV型胶原抗体标记。使用对人IV型胶原特异的抗体,仅在含有成纤维细胞的LDE中观察到血管基底膜的持续标记。在DED中,移植后早期观察到小鼠内皮细胞与人IV型胶原持续关联。在后期,人IV型胶原逐渐消失。另一方面,人表皮下方的真皮-表皮连接处,在两种重建皮肤中都含有人类IV型胶原。用针对人或鼠I型胶原的种属特异性抗体标记显示,鼠I型胶原与人I型胶原的比例随时间增加,这表明DED逐渐被产生鼠胶原的小鼠成纤维细胞侵入。另一方面,在LDE中,先前存在的牛I型胶原逐渐无法检测到,而人I型胶原和弹性纤维则由大量人成纤维细胞沉积。未检测到小鼠I型胶原。总之,将“体外”重建的人皮肤移植到裸鼠身上所做的这些观察结果,对于评估在烧伤治疗中移植真皮基质与表皮片的有用性应该是有意义的。