Department of Surgical and Perioperative Sciences, Surgery, Umeå University, Daniel Naezéns väg, 901 87, Umeå, Sweden.
Department of Surgery, University of Gothenburg, Gothenburg, Sweden.
Hernia. 2022 Dec;26(6):1695-1705. doi: 10.1007/s10029-022-02664-0. Epub 2022 Sep 1.
Autologous full-thickness skin grafting (FTSG) has the potential to become an option in abdominal wall repair. An understanding of tissue remodelling in the extracellular matrix (ECM) is crucial as this interplay determines such parameters as tissue strength and flexibility. This cross-sectional preclinical laboratory study in mice provides information on the distribution of collagen types and matrix metalloproteinases (MMPs) in the ECM of FTSGs in the intraperitoneal and onlay positions compared with internal controls. The aim was to evaluate morphologic changes after tissue remodelling and repair in FTSGs applied in the two positions and to detect any adverse host response.
ECM components were evaluated as follows: qualitative examination of collagen bundle thickness using Picrosirius Red staining (collagen types I, III and IV); and evaluation of collagen types IV and V, as well as MMPs 1, 8 and 9 using immunohistochemical staining. Full-thickness grafts transplanted between female twin mice were examined as this best mimics autologous transplantation.
At 8 weeks, FTSGs in the intraperitoneal position did not show any noticeable differences in morphologic appearance to those in the onlay position. Both intraperitoneal and onlay FTSGs showed increases in the amount of thick collagen bundles compared to internal controls. No correlation was seen between distribution of MMPs 1, 8 or 9 and distribution of collagen types I, III, IV or V.
This preclinical study shows that FTSGs in both intraperitoneal and onlay positions are possible application site options and, by extension, promising application site options for abdominal wall reinforcement in hernia surgery. Clinical studies in humans are required to confirm these findings.
自体全厚皮片移植(FTSG)有可能成为腹壁修复的一种选择。了解细胞外基质(ECM)中的组织重塑至关重要,因为这种相互作用决定了组织强度和柔韧性等参数。这项在小鼠中进行的前瞻性临床前实验室研究提供了 FTSG 在腹膜内和覆盖位置与内部对照相比 ECM 中胶原类型和基质金属蛋白酶(MMPs)分布的信息。目的是评估 FTSG 在两种位置应用后的组织重塑和修复后的形态变化,并检测任何不良的宿主反应。
评估 ECM 成分如下:使用苦味酸天狼星红染色(胶原类型 I、III 和 IV)定性检查胶原束厚度;使用免疫组织化学染色评估胶原类型 IV 和 V 以及 MMPs 1、8 和 9。由于最能模拟自体移植,因此使用雌性双胞胎小鼠之间移植的全厚移植物进行检查。
在 8 周时,腹膜内位置的 FTSG 在形态外观上与覆盖位置的 FTSG 没有明显差异。与内部对照相比,腹膜内和覆盖的 FTSG 均显示出增厚胶原束数量的增加。MMPs 1、8 或 9 的分布与胶原类型 I、III、IV 或 V 的分布之间没有相关性。
这项临床前研究表明,腹膜内和覆盖位置的 FTSG 都是可能的应用部位选择,并且可以扩展到疝修补术中腹壁加强的有前途的应用部位选择。需要进行人体临床研究来证实这些发现。