Naskar Sharmistha, Kumaran Viswanathan, Markandeya Yogananda S, Mehta Bhupesh, Basu Bikramjit
Centre for Biosystems Science and Engineering, Indian Institute of Science, Bangalore, 560012, India; Department of Chemical Engineering, Indian Institute of Science, Bangalore, 560012, India; Laboratory for Biomaterials, Materials Research Centre, Indian Institute of Science, Bangalore, 560012, India; Centres of Excellence and Innovation in Biotechnology - Translational Centre on Biomaterials for Orthopaedic and Dental Applications, Materials Research Centre, IISc, Bangalore, India.
Department of Chemical Engineering, Indian Institute of Science, Bangalore, 560012, India.
Biomaterials. 2020 Jan;226:119522. doi: 10.1016/j.biomaterials.2019.119522. Epub 2019 Oct 9.
A number of bioengineering strategies, using biophysical stimulation, are being explored to guide the human mesenchymal stem cells (hMScs) into different lineages. In this context, we have limited understanding on the transdifferentiation of matured cells to another functional-cell type, when grown with stem cells, in a constrained cellular microenvironment under biophysical stimulation. While addressing such aspects, the present work reports the influence of the electric field (EF) stimulation on the phenotypic and functionality modulation of the coculture of murine myoblasts (C2C12) with hMScs [hMSc:C2C12=1:10] in a custom designed polymethylmethacrylate (PMMA) based microfluidic device with in-built metal electrodes. The quantitative and qualitative analysis of the immunofluorescence study confirms that the cocultured cells in the conditioned medium with astrocytic feed, exhibit differentiation towards neural-committed cells under biophysical stimulation in the range of the endogenous physiological electric field strength (8 ± 0.06 mV/mm). The control experiments using similar culture protocols revealed that while C2C12 monoculture exhibited myotube-like fused structures, the hMScs exhibited the neurosphere-like clusters with SOX2, nestin, βIII-tubulin expression. The electrophysiological study indicates the significant role of intercellular calcium signalling among the differentiated cells towards transdifferentiation. Furthermore, the depolarization induced calcium influx strongly supports neural-like behaviour for the electric field stimulated cells in coculture. The intriguing results are explained in terms of the paracrine signalling among the transdifferentiated cells in the electric field stimulated cellular microenvironment. In summary, the present study establishes the potential for neurogenesis on-chip for the coculture of hMSc and C2C12 cells under tailored electric field stimulation, in vitro.
目前正在探索多种利用生物物理刺激的生物工程策略,以引导人间充质干细胞(hMScs)分化为不同的细胞谱系。在此背景下,我们对于成熟细胞在生物物理刺激下,于受限的细胞微环境中与干细胞共同培养时向另一种功能细胞类型转分化的了解有限。在解决这些问题的过程中,本研究报告了电场(EF)刺激对鼠成肌细胞(C2C12)与hMScs [hMSc:C2C12 = 1:10] 共培养物的表型和功能调节的影响,该共培养物置于定制设计的基于聚甲基丙烯酸甲酯(PMMA)且内置金属电极的微流控装置中。免疫荧光研究的定量和定性分析证实,在内源性生理电场强度(8 ± 0.06 mV/mm)范围内的生物物理刺激下,在含有星形胶质细胞培养液的条件培养基中共培养的细胞表现出向神经定向细胞的分化。使用类似培养方案的对照实验表明,虽然C2C12单培养物表现出肌管样融合结构,但hMScs表现出具有SOX2、巢蛋白、βIII - 微管蛋白表达的神经球样簇。电生理研究表明细胞间钙信号在分化细胞向转分化过程中起重要作用。此外,去极化诱导的钙内流有力地支持了共培养中电场刺激细胞的类神经行为。这些有趣的结果可以通过电场刺激的细胞微环境中转分化细胞之间的旁分泌信号来解释。总之,本研究确定了在体外定制电场刺激下,hMSc和C2C12细胞共培养在芯片上实现神经发生的潜力。