Rennekampff H O, Hansbrough J F, Kiessig V, Abiezzi S, Woods V
Department of Surgery, University of California, San Diego Medical Center 92103, USA.
Surgery. 1996 Jul;120(1):16-22. doi: 10.1016/s0039-6060(96)80235-2.
Burn excision followed by immediate wound coverage has become the clinical standard for managing extensive burn injuries in much of the world. When sufficient autograft skin to achieve permanent wound closure is unavailable, cell culture technology has made the use of cultured human keratinocyte (HK) sheets clinically feasible. Whereas previous techniques have focused on development of multilayered, differentiated HK sheets, our attention has been drawn to using HK in a highly proliferative, less differentiated state. Time requirements for preparation of multistratified cultured HK are high, and preparatory steps may destroy important integrin adhesion molecules.
We describe the use of HK cultured to single layer confluence on a polyurethane membrane(HD), with serum-free medium. HK-HD grafts were transplanted to full-thickness wounds on athymic mice (n = 31). A second group of mice (DG-HK-HD), n = 28) received a living human dermal replacement containing cultured fibroblasts before placement of HK-HD. Control mice received HD alone (n = 4). Basement membrane proteins on healed wounds and surface integrins on cultured HK were identified by means of immunostaining and direct microscopic visualization.
HK cultured just to the confluent state on polyurethane membrane were positive for integrins alpha(5) and alpha(6), major integrins on proliferating HK. Histologic analysis showed epithelialized wounds in all groups after 21 days. Using an anti-human involucrin antibody we demonstrated the presence of HK in 64.5% of the HK-HD group, 61% of the DG-HK-HD group, and 0% in the HD group. Mice that received the living human dermal replacement containing cultured fibroblasts in combination with HK-HD grafts developed a thick, well-vascularized neodermis. Strong laminin and collagen IV staining was observed in wound areas covered with HK.
These data show that full-thickness wounds can be closed by application of a single layer of proliferating HK cultured on a biocompatible polyurethane membrane. This technique is an alternative to the use of multilayered, differentiated HK sheets. Preparation times for HK-HD grafts should be significantly shorter than required for multilayered HK sheets, technical efforts should be less, and more extensive wound areas could be covered.
烧伤切除后立即进行创面覆盖已成为世界上许多地区治疗大面积烧伤的临床标准。当无法获得足够的自体皮来实现永久性创面闭合时,细胞培养技术已使培养的人角质形成细胞(HK)片层在临床上的应用成为可能。以往的技术主要集中在多层、分化的HK片层的开发上,而我们的注意力已转向使用处于高增殖、低分化状态的HK。制备多层培养的HK所需时间较长,且制备步骤可能会破坏重要的整合素黏附分子。
我们描述了在无血清培养基中,将HK培养至在聚氨酯膜(HD)上单层汇合的情况。将HK-HD移植物移植到无胸腺小鼠的全层伤口上(n = 31)。第二组小鼠(DG-HK-HD,n = 28)在植入HK-HD之前接受含有培养成纤维细胞的活性人真皮替代物。对照小鼠仅接受HD(n = 4)。通过免疫染色和直接显微镜观察鉴定愈合伤口上的基底膜蛋白和培养的HK上的表面整合素。
在聚氨酯膜上培养至汇合状态的HK对整合素α(5)和α(6)呈阳性,这是增殖HK上的主要整合素。组织学分析显示21天后所有组的伤口均已上皮化。使用抗人内披蛋白抗体,我们在HK-HD组的64.5%、DG-HK-HD组的61%以及HD组的0%中证实了HK的存在。接受含有培养成纤维细胞的活性人真皮替代物与HK-HD移植物联合治疗的小鼠形成了厚且血管化良好的新真皮。在覆盖有HK的伤口区域观察到强烈的层粘连蛋白和IV型胶原染色。
这些数据表明,应用单层在生物相容性聚氨酯膜上培养的增殖HK可闭合全层伤口。该技术是使用多层、分化的HK片层的替代方法。HK-HD移植物的制备时间应明显短于多层HK片层所需时间,技术操作应更少,且可覆盖更广泛的伤口区域。