Houston, Texas; and Magdeburg, Germany From the Departments of Molecular Pathology and Plastic Surgery, University of Texas M. D. Anderson Cancer Center; the Department of Radiology, Otto von Guericke University; and InGeneron Inc.
Plast Reconstr Surg. 2010 Jan;125(1):63-73. doi: 10.1097/PRS.0b013e3181c2a59a.
Transplantation of adipose tissue-resident mesenchymal stem cells has been found to contribute to the establishment of a supportive fibrovascular network. The authors sought to evaluate the potential of human adipose tissue-derived stem cells to integrate with nonanimal stabilized hyaluronic acid as a novel injectable soft-tissue filler.
Cell proliferation was measured by bromodeoxyuridine incorporation. Interactions of adipose tissue-derived stem cells with hyaluronic acid were documented by scanning electron microscopy. The effect of this combination on procollagen mRNA was assessed by real-time polymerase chain reaction. The potential therapeutic effects were evaluated in an athymic murine photoaged skin model by histology and by high-resolution magnetic resonance imaging. Angiogenesis was assessed by microvessel density analysis.
Under in vitro culture conditions, the authors found an equal proliferation capacity of adipose tissue-derived stem cells grown on hyaluronic acid versus controls. Scanning electron microscopy showed enhanced establishment of complex microvillous networks in adipose tissue-derived stem cells adherent to hyaluronic acid compared with controls. Adipose tissue-derived stem cells and hyaluronic acid induced a significant increase in procollagen 1-alpha-2 mRNA expression compared with controls. In an athymic murine photoaged skin model, injection of this combination ablated photoinduced skin wrinkles. Magnetic resonance imaging revealed a consistent and stable volume fill by adipose tissue-derived stem cells and nonanimal stabilized hyaluronic acid at 3 weeks. Adipose tissue-derived stem cells actively incorporated into the hyaluronic acid fill and showed an organized fibrovascular network at 3 weeks.
The combination of adipose tissue-derived stem cells and nonanimal stabilized hyaluronic acid holds promise as a tool with which to achieve lasting volume fill in reconstructive surgical soft-tissue augmentation.
脂肪组织驻留间充质干细胞的移植已被发现有助于建立支持性纤维血管网络。作者试图评估人脂肪组织来源的干细胞与非动物稳定透明质酸整合的潜力,作为一种新型的可注射软组织填充剂。
通过溴脱氧尿苷掺入测量细胞增殖。扫描电子显微镜记录脂肪组织来源的干细胞与透明质酸的相互作用。通过实时聚合酶链反应评估这种组合对原胶原蛋白 mRNA 的影响。通过组织学和高分辨率磁共振成像评估该组合在无胸腺鼠光老化皮肤模型中的潜在治疗效果。通过微血管密度分析评估血管生成。
在体外培养条件下,作者发现生长在透明质酸上的脂肪组织来源的干细胞与对照相比具有相同的增殖能力。扫描电子显微镜显示,与对照相比,在附着于透明质酸的脂肪组织来源的干细胞中,复杂的微绒毛网络的建立得到增强。与对照相比,脂肪组织来源的干细胞和透明质酸诱导胶原 1 型-α2 mRNA 表达显著增加。在无胸腺鼠光老化皮肤模型中,该组合的注射消除了光诱导的皮肤皱纹。磁共振成像显示,在 3 周时,脂肪组织来源的干细胞和非动物稳定透明质酸的一致和稳定的体积填充。脂肪组织来源的干细胞积极整合到透明质酸填充中,并在 3 周时显示出有组织的纤维血管网络。
脂肪组织来源的干细胞与非动物稳定透明质酸的组合有望成为实现重建性外科软组织增强持久体积填充的工具。