Silk fibroin induces chondrogenic differentiation of canine adipose-derived multipotent mesenchymal stromal cells/mesenchymal stem cells

被引:17
作者
Voga, Metka [1 ]
Drnovsek, Natasa [2 ]
Novak, Sasa [2 ]
Majdic, Gregor [1 ,3 ]
机构
[1] Univ Ljubljana, Vet Fac, Inst Preclin Sci, Gerbiceva 60, Ljubljana 1000, Slovenia
[2] Jozef Stefan Inst, Dept Nanostruct Mat, Ljubljana, Slovenia
[3] Univ Maribor, Med Sch, Inst Physiol, Maribor, Slovenia
关键词
Mesenchymal stem cells; multipotent mesenchymal stromal cells; dog; silk fibroin; chondrogenic differentiation; IN-VITRO; MARROW; SCAFFOLDS; BIOMATERIALS; GROWTH;
D O I
10.1177/2041731419835056
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Under appropriate culture conditions, mesenchymal stem cells (MSC), also called more properly multipotent mesenchymal stromal cells (MMSC), can be induced toward differentiation into different cell lineages. In order to guide stem cell fate within an environment resembling the stem cell niche, different biomaterials are being developed. In the present study, we used silk fibroin (SF) as a biomaterial supporting the growth of MMSC and studied its effect on chondrogenesis of canine adipose-derived MMSC (cADMMSC). Adipose tissue was collected from nine privately owned dogs. MMSC were cultured on SF films and SF scaffolds in a standard cell culture medium. Cell morphology was evaluated by scanning electron microscopy (SEM). Chondrogenic differentiation was evaluated by alcian blue staining and mRNA expression of collagen type 1, collagen type 2, Sox9, and Aggrecan genes. cADMMSC cultured on SF films and SF scaffolds stained positive using alcian blue. SEM images revealed nodule-like structures with matrix vesicles and fibers resembling chondrogenic nodules. Gene expression of chondrogenic markers Sox9 and Aggrecan were statistically significantly upregulated in cADMMSC cultured on SF films in comparison to negative control cADMMSC. This result suggests that chondrogenesis of cADMMSC could occur when cells were grown on SF films in a standard cell culture medium without specific culture conditions, which were previously considered necessary for induction of chondrogenic differentiation.
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页数:14
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