Institute of Medical Physics and Biophysics, Faculty of Medicine, University of Leipzig, D-04107 Leipzig, Germany.
Anal Biochem. 2012 Feb 15;421(2):791-3. doi: 10.1016/j.ab.2011.11.002. Epub 2011 Nov 12.
The self-healing capacity of skin is limited, and medical intervention is often unavoidable. Skin may be generated ex vivo from cultured fibroblasts. Because the molecular composition of de novo formed skin (mostly collagen and glycosaminoglycans [GAGs]) is crucial, analytical methods are required for the quality control of tissue-engineered products. Here, we show that matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) of fibroblast cultures subsequent to digestion with chondroitinase ABC is a reliable and fast method to monitor the GAG content of native and bioengineered skin. Furthermore, the supplementation of the fibroblast medium with ¹³C-labeled glucose provides insights into the biosynthesis of GAGs.
皮肤的自我修复能力有限,医学干预往往是不可避免的。皮肤可以从培养的成纤维细胞中体外生成。由于新形成的皮肤的分子组成(主要是胶原蛋白和糖胺聚糖[GAGs])至关重要,因此需要分析方法来控制组织工程产品的质量。在这里,我们表明,用软骨素酶 ABC 消化后,基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)分析成纤维细胞培养物是一种可靠且快速的方法,可以监测天然和生物工程皮肤的 GAG 含量。此外,在成纤维细胞培养基中补充¹³C 标记的葡萄糖可以深入了解 GAG 的生物合成。