Key Laboratory of Gene Engineering of the Ministry of Education, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China; Wake Forest Institute for Regenerative Medicine, 391 Technology Way, Winston-Salem, NC, USA.
Wake Forest Institute for Regenerative Medicine, 391 Technology Way, Winston-Salem, NC, USA.
Acta Biomater. 2017 Oct 15;62:222-233. doi: 10.1016/j.actbio.2017.08.022. Epub 2017 Aug 17.
Myogenic differentiation, cell fusion, and myotube formation of skeletal muscle progenitor cells (SMPCs) have key roles during skeletal muscle development and repair. However, after isolation from living tissue and transition to culture dishes, SMPCs gradually lose their function and stop propagating due to the absence of extracellular matrix (ECM). Despite encouraging results of experiments using ECM components in cell culture for maintenance and propagation of some tissue types, the benefits of this approach on SMPC culture are limited, because the bioactive molecules and proteins instantly release and are degraded during culture. In this study, we developed a novel approach to enhance the proliferation and differentiation of human skeletal muscle progenitor cells (hSMPCs) in vitro with skeletal muscle ECM in combination with a modified alginate hydrogel conjugated with gelatin and heparin (Alg-G-H) as a substrate. This Alg-G-H substrate, together with skeletal muscle ECM, significantly enhanced cell expansion, differentiation, and maturation of hSMPCs compared with individual substrata (i.e. gelatin, Matrigel®, or ECM alone). In Western-blot and immunocytochemical analyses, the Alg-G-H-ECM predominantly enhanced expression of skeletal myogenesis markers (MyoD, Myf5, Myogenin, Desmin and Myosin) and myotube formation in hSMPCs. This study demonstrated that combining Alg-G-H substrates with skeletal muscle ECM modulated homeostasis of cell proliferation, differentiation, and maturation of hSMPCs by releasing signaling molecules and growth factors. This technique could be a cost-effective tool for in vitro skeletal muscle cell differentiation and maturation, with potential applications in tissue regeneration and drug development.
Alginate based biomaterials are commonly used in tissue engineering and regenerative medicine field, however, the inefficient sequestration of growth factors restricted its utilization. In this study, a novel alginate based substrates was produced covalently modified with gelatin and heparin, in order to capture more effective cytokines and proteins in the culture milieu, keep homeostasis for cell survival and tissue regeneration with growth factor sequestration and long-term release capacities. Combining with skeletal muscle derived ECM, the modified Alginate-Gelatin-Heparin gel could most effectively mimic the tissue specific microenvironment to support skeletal muscle progenitor cells proliferation, differentiation and myotube formation. Additionally, the economical and practical features will make it more promising in high-throughput application for regenerative medicine research.
成肌分化、细胞融合和肌管形成在骨骼肌祖细胞(SMPCs)的骨骼肌发育和修复中起着关键作用。然而,SMPCs 从活体组织中分离出来并转移到培养皿后,由于缺乏细胞外基质(ECM),其功能逐渐丧失,增殖停止。尽管在细胞培养中使用 ECM 成分来维持和增殖某些组织类型的实验取得了令人鼓舞的结果,但这种方法对 SMPC 培养的益处有限,因为生物活性分子和蛋白质在培养过程中会立即释放并降解。在这项研究中,我们开发了一种新方法,通过将骨骼肌 ECM 与经过改良的明胶和肝素结合的藻酸盐水凝胶(Alg-G-H)结合作为基质,来增强体外人骨骼肌祖细胞(hSMPCs)的增殖和分化。与单独的基质(即明胶、Matrigel®或 ECM 单独)相比,这种 Alg-G-H 基质与骨骼肌 ECM 一起,可显著促进 hSMPCs 的细胞扩增、分化和成熟。在 Western blot 和免疫细胞化学分析中,Alg-G-H-ECM 主要增强了 hSMPCs 中骨骼肌成肌发生标志物(MyoD、Myf5、Myogenin、Desmin 和 Myosin)的表达和肌管形成。这项研究表明,Alg-G-H 基质与骨骼肌 ECM 结合可通过释放信号分子和生长因子来调节 hSMPCs 的细胞增殖、分化和成熟的动态平衡。该技术可能是体外骨骼肌细胞分化和成熟的一种具有成本效益的工具,在组织再生和药物开发方面具有潜在应用。
藻酸盐基生物材料常用于组织工程和再生医学领域,然而,其生长因子的低效捕获限制了其应用。在这项研究中,我们制备了一种新型的藻酸盐基基质,通过共价修饰明胶和肝素,以在培养环境中捕获更有效的细胞因子和蛋白质,通过生长因子的捕获和长期释放能力保持细胞存活和组织再生的动态平衡。结合来源于骨骼肌的 ECM,经过改良的藻酸盐-明胶-肝素凝胶可以最有效地模拟组织特异性微环境,以支持骨骼肌祖细胞的增殖、分化和肌管形成。此外,其经济实用的特点使其在再生医学研究的高通量应用中更具前景。