Klar Agnieszka S, Böttcher-Haberzeth Sophie, Biedermann Thomas, Schiestl Clemens, Reichmann Ernst, Meuli Martin
University Children's Hospital Zurich, Tissue Biology Research Unit, Zurich, Switzerland.
Pediatr Surg Int. 2014 Feb;30(2):223-31. doi: 10.1007/s00383-013-3451-0.
Bioengineered dermo-epidermal skin analogs containing melanocytes represent a promising approach to cover large skin defects including restoration of the patient's own skin color. So far, little is known about the development of blood and lymphatic vessels in pigmented skin analogs after transplantation. In this experimental study, we analyzed the advancement and differences of host blood and lymphatic vessel ingrowth into light- and dark-pigmented human tissue-engineered skin analogs in a rat model.
Keratinocytes, melanocytes, and fibroblasts from light- and dark-pigmented skin biopsies were isolated, cultured, and expanded. For each donor, melanocytes and keratinocytes were seeded in ratios of 1:1, 1:5, and 1:10 onto fibroblast-containing collagen gels. The skin analogs were subsequently transplanted onto full-thickness wounds of immuno-incompetent rats and quantitatively analyzed for vascular and lymphatic vessel density after 8 and 15 weeks.
The skin analogs revealed a significant difference in vascularization patterns between light- and dark-pigmented constructs after 8 weeks, with a higher amount of blood vessels in light compared to dark skin. In contrast, no obvious difference could be detected within the light- and dark-pigmented group when varying melanocyte/keratinocyte ratios were used. However, after 15 weeks, the aforementioned difference in blood vessel density between light and dark constructs could no longer be detected. Regarding lymphatic vessels, light and dark analogs showed similar vessel density after 8 and 15 weeks, while there were generally less lymphatic than blood vessels.
These data suggest that, at least during early skin maturation, keratinocytes, melanocytes, and fibroblasts from different skin color types used to construct pigmented dermo-epidermal skin analogs have distinct influences on the host tissue after transplantation. We speculate that different VEGF expression patterns might be involved in this disparate revascularization pattern observed.
含有黑素细胞的生物工程真皮 - 表皮皮肤类似物是覆盖大面积皮肤缺损(包括恢复患者自身肤色)的一种有前景的方法。到目前为止,关于移植后色素沉着皮肤类似物中血管和淋巴管的发育情况知之甚少。在本实验研究中,我们在大鼠模型中分析了宿主血管和淋巴管向内生长到浅色和深色色素沉着的人体组织工程皮肤类似物中的进展及差异。
从浅色和深色色素沉着的皮肤活检组织中分离、培养并扩增角质形成细胞、黑素细胞和成纤维细胞。对于每个供体,黑素细胞和角质形成细胞按1:1、1:5和1:10的比例接种到含成纤维细胞的胶原凝胶上。随后将皮肤类似物移植到免疫缺陷大鼠的全层伤口上,并在8周和15周后对血管和淋巴管密度进行定量分析。
8周后,浅色和深色构建体的皮肤类似物在血管化模式上显示出显著差异,浅色皮肤中的血管数量比深色皮肤多。相比之下,当使用不同的黑素细胞/角质形成细胞比例时,浅色和深色色素沉着组之间未检测到明显差异。然而,15周后,浅色和深色构建体之间上述血管密度差异不再能被检测到。关于淋巴管,浅色和深色类似物在8周和15周后显示出相似的血管密度,而淋巴管通常比血管少。
这些数据表明,至少在皮肤早期成熟过程中,用于构建色素沉着真皮 - 表皮皮肤类似物的不同肤色类型的角质形成细胞、黑素细胞和成纤维细胞在移植后对宿主组织有不同影响。我们推测不同的血管内皮生长因子(VEGF)表达模式可能与观察到的这种不同的再血管化模式有关。