Ahtiainen Katja, Sippola Laura, Nurminen Manu, Mannerström Bettina, Haimi Suvi, Suuronen Riitta, Hyttinen Jari, Ylikomi Timo, Kellomäki Minna, Miettinen Susanna
Department of Cell Biology, School of Medicine, University of Tampere, Finland; Adult Stem Cells, Institute of Biomedical Technology, University of Tampere, Finland; BioMediTech, Tampere, Finland; Science Center, Tampere University Hospital, Finland.
J Tissue Eng Regen Med. 2015 Jan;9(1):55-65. doi: 10.1002/term.1614. Epub 2012 Oct 22.
The performance of biodegradable knitted and rolled 3-dimensional (3D) polylactide-based 96/4 scaffolds modified with bioactive glass (BaG) 13-93, chitosan and both was compared with regard to the viability, proliferation and chondrogenic differentiation of rabbit adipose stem cells (ASCs). Scaffold porosities were determined by micro-computed tomography (μCT). Water absorption and degradation of scaffolds were studied during 28-day hydrolysis in Tris-buffer. Viability, number and differentiation of ASCs in PLA96/4 scaffolds were examined in vitro. The dimensions of the scaffolds were maintained during hydrolysis and mass loss was detected only in the BaG13-93 containing scaffolds. ASCs adhered and proliferated on each scaffold type. Cell aggregation and expression of chondral matrix components improved in all scaffold types in chondrogenic medium. Signs of hypertrophy were detected in the modified scaffolds but not in the plain PLA96/4 scaffold. Chondrogenic differentiation was most enhanced in the presence of chitosan. These findings indicate that the plain P scaffold provided a good 3D-matrix for ASC proliferation whereas the addition of chitosan to the PLA96/4 scaffold induced chondrogenic differentiation independent of the medium. Accordingly, a PLA96/4 scaffold modified by chitosan could provide a functional and bioactive basis for tissue-engineered chondral implants.
将用生物活性玻璃(BaG)13 - 93、壳聚糖以及二者对可生物降解的针织和卷绕三维(3D)聚丙交酯基96/4支架进行改性后的性能,在兔脂肪干细胞(ASC)的活力、增殖和软骨形成分化方面进行了比较。通过微计算机断层扫描(μCT)测定支架孔隙率。在Tris缓冲液中进行28天水解期间研究了支架的吸水性和降解情况。在体外检查了PLA96/4支架中ASC的活力、数量和分化情况。水解过程中支架尺寸保持不变,仅在含BaG13 - 93的支架中检测到质量损失。ASC在每种支架类型上均能黏附并增殖。在软骨形成培养基中,所有支架类型中细胞聚集和软骨基质成分的表达均有所改善。在改性支架中检测到肥大迹象,但在普通PLA96/4支架中未检测到。壳聚糖存在时软骨形成分化增强最为明显。这些发现表明,普通P支架为ASC增殖提供了良好的三维基质,而向PLA96/4支架中添加壳聚糖可诱导软骨形成分化,且与培养基无关。因此,壳聚糖改性的PLA96/4支架可为组织工程软骨植入物提供功能性和生物活性基础。