Olsen T R, Mattix B, Casco M, Herbst A, Williams C, Tarasidis A, Simionescu D, Visconti R P, Alexis F
Department of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA.
Department of Bioengineering, Clemson University, 301 Rhodes Research Center, Clemson, SC 29634, USA.
Acta Biomater. 2015 Feb;13:188-98. doi: 10.1016/j.actbio.2014.11.024. Epub 2014 Nov 20.
Cellular spheroids were investigated as tissue-engineered building blocks that can be fused to form functional tissue constructs. While spheroids can be assembled using passive contacts for the fusion of complex tissues, physical forces can be used to promote active contacts to improve tissue homogeneity and accelerate tissue fusion. Understanding the mechanisms affecting the fusion of spheroids is critical to fabricating tissues. Here, manipulation of the spheroid composition was used to accelerate the fusion process mediated by magnetic forces. The Janus structure of magnetic cellular spheroids spatially controls iron oxide magnetic nanoparticles (MNPs) to form two distinct domains: cells and extracellular MNPs. Studies were performed to evaluate the influence of extracellular matrix (ECM) content and cell number on the fusion of Janus magnetic cellular spheroids (JMCSs). Results showed that the integration of iron oxide MNPs into spheroids increased the production of collagen over time when compared to spheroids without MNPs. The results also showed that ring tissues composed of JMCSs with high ECM concentrations and high cell numbers fused together, but exhibited less contraction when compared to their lower concentration counterparts. Results from spheroid fusion in capillary tubes showed that low ECM concentrations and high cell numbers experienced more fusion and cellular intermixing over time when compared to their higher counterparts. These findings indicate that cell-cell and cell-matrix interactions play an important role in regulating fusion, and this understanding sets the rationale of spheroid composition to fabricate larger and more complex tissue-engineered constructs.
细胞球体作为组织工程构建块进行了研究,其可融合形成功能性组织构建体。虽然可以使用被动接触来组装球体以实现复杂组织的融合,但物理力可用于促进主动接触,以改善组织同质性并加速组织融合。了解影响球体融合的机制对于制造组织至关重要。在此,通过操纵球体组成来加速由磁力介导的融合过程。磁性细胞球体的Janus结构在空间上控制氧化铁磁性纳米颗粒(MNP)形成两个不同的区域:细胞和细胞外MNP。进行了研究以评估细胞外基质(ECM)含量和细胞数量对Janus磁性细胞球体(JMCS)融合的影响。结果表明,与不含MNP的球体相比,随着时间的推移,氧化铁MNP整合到球体中会增加胶原蛋白的产生。结果还表明,由高ECM浓度和高细胞数量的JMCS组成的环形组织融合在一起,但与低浓度对应物相比收缩较小。毛细管中球体融合的结果表明,与较高浓度的对应物相比,低ECM浓度和高细胞数量随着时间的推移经历了更多的融合和细胞混合。这些发现表明,细胞 -细胞和细胞 - 基质相互作用在调节融合中起重要作用,并且这种认识为制造更大、更复杂的组织工程构建体奠定了球体组成的理论基础。