Zürich, Switzerland; and Rostock, Germany From the Division of Plastic and Reconstructive Surgery and the Division of Cardiovascular Surgery, Department of Surgery, University Hospital Zurich, and the Institute for Experimental Surgery, University of Rostock.
Plast Reconstr Surg. 2010 Jul;126(1):61-70. doi: 10.1097/PRS.0b013e3181da87f6.
In the era of tissue engineering, the physiologic process of skin graft revascularization remains unclear, preventing the successful development of skin substitutes. Therefore, the authors developed a new in vivo model with which to visualize the process of engraftment and its microvascular architecture. The aim of this study was to specifically investigate the vascular transformations within the skin graft to gain applicable knowledge on how vascular processes during engraftment occur.
Microsurgical preparation of the modified dorsal skinfold chamber including autologous skin grafting was performed in male C57BL/6J mice (n = 10). In addition, immunohistochemistry of angiogenic factors, endothelial cells, and pericytes, and corrosion casting were performed to further characterize the specific mechanisms.
The graft exhibited capillary widening starting at day 3, resulting in the temporary formation of spherical protrusions at the graft capillary divisions starting in the center of the graft 24 to 48 hours after revascularization. Confocal microscopy showed the simultaneous expression of CD31 and desmin. Corrosion casting and evaluation by light microscopy and scanning electron microscopy showed the three-dimensional formation of capillaries in the wound bed that connected to the preexisting capillary loops of the skin graft.
The authors were able to show for the first time a temporary angiogenic response within the capillaries of the skin graft. This most likely represents a reaction to reperfusion allowing the supply of proangiogenic factors to the hypoxic skin graft. The detection of an angiogenic response within the graft capillaries is for the first time made possible in the newly developed model and is therefore completely novel.
在组织工程学时代,皮肤移植物再血管化的生理过程仍不清楚,这阻碍了皮肤替代物的成功开发。因此,作者开发了一种新的体内模型,以可视化植入过程及其微血管结构。本研究的目的是专门研究移植物内的血管转化,以获得有关植入过程中血管过程如何发生的有用知识。
在雄性 C57BL/6J 小鼠(n = 10)中进行改良背侧皮褶室的显微外科准备,包括自体皮肤移植。此外,还进行了血管生成因子、内皮细胞和周细胞的免疫组织化学和腐蚀铸造,以进一步阐明特定机制。
移植物在第 3 天开始出现毛细血管扩张,导致在再血管化后 24 至 48 小时内,移植物毛细血管分支的中心开始出现球形突起,暂时形成球形突起。共聚焦显微镜显示 CD31 和结蛋白同时表达。腐蚀铸造和光镜及扫描电镜评估显示,伤口床内形成了与皮肤移植物原有毛细血管环相连的三维毛细血管。
作者首次能够显示皮肤移植物内毛细血管的暂时血管生成反应。这很可能是对再灌注的反应,允许缺氧皮肤移植物供应促血管生成因子。在新开发的模型中首次能够检测到移植物毛细血管内的血管生成反应,因此这是完全新颖的。