Department of Veterinary Medical Sciences, University of Bologna, via Tolara di Sopra 50, 40064, Ozzano Emilia, BO, Italy.
Department for Biomedical and Neuromotor Sciences, University of Bologna, via Irnerio 48, 40126, Bologna, BO, Italy.
Stem Cell Rev Rep. 2018 Aug;14(4):574-584. doi: 10.1007/s12015-018-9803-3.
Wharton's jelly (WJ) is an important source of mesenchymal stem cells (MSCs) both in human and other animals. The aim of this study was to compare human and equine WJMSCs. Human and equine WJMSCs were isolated and cultured using the same protocols and culture media. Cells were characterized by analysing morphology, growth rate, migration and adhesion capability, immunophenotype, differentiation potential and ultrastructure. Results showed that human and equine WJMSCs have similar ultrastructural details connected with intense synthetic and metabolic activity, but differ in growth, migration, adhesion capability and differentiation potential. In fact, at the scratch assay and transwell migration assay, the migration ability of human WJMSCs was higher (P < 0.05) than that of equine cells, while the volume of spheroids obtained after 48 h of culture in hanging drop was larger than the volume of equine ones (P < 0.05), demonstrating a lower cell adhesion ability. This can also revealed in the lower doubling time of equine cells (3.5 ± 2.4 days) as compared to human (6.5 ± 4.3 days) (P < 0.05), and subsequently in the higher number of cell doubling after 44 days of culture observed for the equine (20.3 ± 1.7) as compared to human cells (8.7 ± 2.4) (P < 0.05), and to the higher (P < 0.05) ability to form fibroblast colonies at P3. Even if in both species tri-lineage differentiation was achieved, equine cells showed an higher chondrogenic and osteogenic differentiation ability (P < 0.05). Our findings indicate that, although the ultrastructure demonstrated a staminal phenotype in human and equine WJMSCs, they showed different properties reflecting the different sources of MSCs.
华通氏胶(WJ)是人类和其他动物间充质干细胞(MSC)的重要来源。本研究旨在比较人源和马源 WJMSCs。采用相同的方案和培养基分离培养人源和马源 WJMSCs。通过分析形态、生长速度、迁移和黏附能力、免疫表型、分化潜能和超微结构对细胞进行鉴定。结果表明,人源和马源 WJMSCs 的超微结构细节相似,均与强烈的合成和代谢活性有关,但在生长、迁移、黏附能力和分化潜能方面存在差异。事实上,在划痕实验和 Transwell 迁移实验中,人源 WJMSCs 的迁移能力更高(P < 0.05),而在悬滴培养 48 h 后获得的球体体积大于马源细胞(P < 0.05),表明其细胞黏附能力较低。这也反映在马源细胞的倍增时间(3.5 ± 2.4 天)较人源细胞(6.5 ± 4.3 天)短(P < 0.05),随后在培养 44 天后,马源细胞的细胞倍增数(20.3 ± 1.7)高于人源细胞(8.7 ± 2.4)(P < 0.05),并且马源细胞在第 P3 代形成成纤维细胞集落的能力更高(P < 0.05)。尽管在两种细胞系中均实现了三系分化,但马源细胞显示出更高的成软骨和成骨分化能力(P < 0.05)。我们的研究结果表明,尽管超微结构显示出人源和马源 WJMSCs 具有干细胞表型,但它们表现出不同的特性,反映了不同来源的 MSC。