McCorry Mary Clare, Puetzer Jennifer L, Bonassar Lawrence J
Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Sibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, USA.
Stem Cell Res Ther. 2016 Mar 12;7:39. doi: 10.1186/s13287-016-0301-8.
Bone marrow mesenchymal stem cells (MSCs) have shown positive therapeutic effects for meniscus regeneration and repair. Preliminary in vitro work has indicated positive results for MSC applications for meniscus tissue engineering; however, more information is needed on how to direct MSC behavior. The objective of this study was to examine the effect of MSC co-culture with primary meniscal fibrochondrocytes (FCCs) in a three-dimensional collagen scaffold in fibrochondrogenic media. Co-culture of MSCs and FCCs was hypothesized to facilitate the transition of MSCs to a FCC cell phenotype as measured by matrix secretion and morphology.
MSCs and FCCs were isolated from bovine bone marrow and meniscus, respectively. Cells were seeded in a 20 mg/mL high-density type I collagen gel at MSC:FCC ratios of 0:100, 25:75, 50:50, 75:25, and 100:0. Constructs were cultured for up to 2 weeks and then analyzed for cell morphology, glycosaminoglycan content, collagen content, and production of collagen type I, II, and X.
Cells were homogeneously mixed throughout the scaffold and cells had limited direct cell-cell contact. After 2 weeks in culture, MSCs transitioned from a spindle-like morphology toward a rounded phenotype, while FCCs remained rounded throughout culture. Although MSC shape changed with culture, the overall size was significantly larger than FCCs throughout culture. While 75:25 and 100:0 (MSC mono-culture) culture groups produced significantly more glycosaminoglycan (GAG)/DNA than FCCs in mono-culture, GAG retention was highest in 50:50 co-cultures. Similarly, the aggregate modulus was highest in 100:0 and 50:50 co-cultures. All samples contained both collagen types I and II after 2 weeks, and collagen type X expression was evident only in MSC mono-culture gels.
MSCs shift to a FCC morphology in both mono- and co-culture. Co-culture reduced hypertrophy by MSCs, indicated by collagen type X. This study shows that MSC phenotype can be influenced by indirect homogeneous cell culture in a three-dimensional gel, demonstrating the applicability of MSCs in meniscus tissue engineering applications.
骨髓间充质干细胞(MSCs)已显示出对半月板再生和修复的积极治疗效果。初步的体外研究表明,MSCs应用于半月板组织工程有积极结果;然而,关于如何引导MSCs行为还需要更多信息。本研究的目的是在三维胶原支架中,在纤维软骨生成培养基中检测MSCs与原代半月板纤维软骨细胞(FCCs)共培养的效果。假设MSCs与FCCs共培养可促进MSCs向FCC细胞表型转变,通过基质分泌和形态学进行测量。
分别从牛骨髓和半月板中分离出MSCs和FCCs。将细胞以MSCs:FCCs比例为0:100、25:75、50:50、75:25和100:0接种到20 mg/mL的高密度I型胶原凝胶中。构建物培养长达2周,然后分析细胞形态、糖胺聚糖含量、胶原含量以及I、II和X型胶原的产生。
细胞在整个支架中均匀混合,细胞间直接接触有限。培养2周后,MSCs从纺锤形形态转变为圆形表型,而FCCs在整个培养过程中保持圆形。虽然MSCs形状随培养而改变,但其总体大小在整个培养过程中明显大于FCCs。虽然75:25和100:0(MSCs单培养)培养组产生的糖胺聚糖(GAG)/DNA比FCCs单培养组显著更多,但GAG保留率在50:50共培养中最高。同样,聚集体模量在100:0和50:50共培养中最高。2周后所有样本均含有I型和II型胶原,X型胶原表达仅在MSCs单培养凝胶中明显。
MSCs在单培养和共培养中均转变为FCC形态。共培养减少了MSCs的肥大,以X型胶原表示。本研究表明,MSCs表型可受三维凝胶中间接均匀细胞培养的影响,证明了MSCs在半月板组织工程应用中的适用性。