Hyaluronic Acid-Coated Melt Electrowritten Scaffolds Promote Myoblast Attachment, Alignment, and Differentiation.

IF 3.5 4区 医学 Q3 BIOPHYSICS
Cellular and molecular bioengineering Pub Date : 2025-09-04 eCollection Date: 2025-10-01 DOI:10.1007/s12195-025-00865-y
Alycia N Galindo, Alyssa K Chi, Ievgenii Liashenko, Kelly L O'Neill, Chandler L Asnes, Ruchi Sharma, Jenna D Khachatourian, Armaan Hajarizadeh, Paul D Dalton, Marian H Hettiaratchi
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引用次数: 0

Abstract

Purpose: In muscle tissues, anisotropic cell alignment is essential for optimal muscle fiber development and function. Biomaterials for muscle tissue engineering must guide cellular alignment while supporting cell proliferation and myogenic differentiation.

Methods: Here, we describe the fabrication of a tissue-engineered construct consisting of a scaffold of aligned poly(ε-caprolactone) (PCL) microfibers coated in a dynamic covalent hydrazone crosslinked hyaluronic acid (HA) hydrogel to support myoblast attachment, myoblast alignment, and myotube formation. Norbornene modification of HA further enabled functionalization with fibronectin-derived arginine-glycine-aspartic acid (RGD) peptide. Scaffolds were fabricated using melt electrowriting (MEW), a three-dimensional (3D)-printing technique that uses stabilization of fluid columns to produce precisely aligned polymeric microfibers. We evaluated C2C12 mouse skeletal myoblasts cultured on non-coated, HA-coated, and HA-RGD-coated MEW scaffolds with fiber diameters of 10, 20, and 30 µm using immunocytochemistry and creatine kinase activity assays. We further evaluated the mechanical properties of 20 µm fiber scaffolds and their effect on myogenic gene expression and alpha-actinin protein expression of C2C12 myoblasts undergoing differentiation.

Results: HA-coated and HA-RGD-coated scaffolds increased attachment of C2C12 myoblasts on all fiber diameters compared to non-coated scaffolds, with HA-RGD-coated scaffolds demonstrating the highest cell attachment. All scaffolds supported cellular alignment along the fibers. Cells differentiated on scaffolds showed anisotropic alignment with increased myotube formation on HA-coated and HA-RGD-coated scaffolds as demonstrated by myosin heavy chain (MHC) staining and by the presence of striations on HA-coated scaffolds visualized with alpha-actinin staining. Increased creatine kinase activity and myogenic gene expression on day 5 further indicated myotube formation on all scaffolds, with HA-coated scaffolds significantly increasing the expression of several key myogenic markers.

Conclusion: This unique combination of tunable biophysical and biochemical cues enables the creation of a biomimetic tissue engineered scaffold, providing a platform for new therapeutic approaches for muscle regeneration.

Supplementary information: The online version contains supplementary material available at 10.1007/s12195-025-00865-y.

Abstract Image

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透明质酸包覆熔融电写支架促进成肌细胞附着、排列和分化。
目的:在肌肉组织中,各向异性细胞排列对于肌肉纤维的最佳发育和功能至关重要。用于肌肉组织工程的生物材料必须引导细胞排列,同时支持细胞增殖和成肌分化。方法:在这里,我们描述了一种组织工程结构的制备,该结构由排列的聚(α -己内酯)(PCL)微纤维支架组成,该支架包裹在动态共价肼交联透明质酸(HA)水凝胶中,以支持成肌细胞附着、成肌细胞排列和肌管形成。降冰片烯修饰的HA进一步实现了纤维连接素衍生的精氨酸-甘氨酸-天冬氨酸(RGD)肽的功能化。支架是用熔体电写(MEW)制造的,这是一种三维(3D)打印技术,利用流体柱的稳定性来生产精确排列的聚合物微纤维。我们对C2C12小鼠骨骼肌母细胞在纤维直径分别为10、20和30µm的未包被、ha包被和ha - rgd包被的MEW支架上培养进行免疫细胞化学和肌酸激酶活性测定。我们进一步评估了20µm纤维支架的力学性能及其对处于分化状态的C2C12成肌细胞的成肌基因表达和α - actiin蛋白表达的影响。结果:与未包被支架相比,ha包被支架和ha - rgd包被支架增加了C2C12成肌细胞在所有纤维直径上的附着,ha - rgd包被支架显示出最高的细胞附着。所有支架都支持细胞沿纤维排列。肌球蛋白重链(MHC)染色和α -肌动蛋白染色显示,ha包被和ha- rgd包被支架上分化的细胞呈各向异性排列,肌管形成增加。第5天肌酸激酶活性和肌源性基因表达的增加进一步表明所有支架上都有肌管形成,ha包被支架显著增加了几个关键肌源性标志物的表达。结论:这种独特的可调生物物理和生化线索的组合使仿生组织工程支架的创建成为可能,为肌肉再生的新治疗方法提供了平台。补充信息:在线版本包含补充资料,可在10.1007/s12195-025-00865-y获得。
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来源期刊
CiteScore
5.60
自引率
3.60%
发文量
30
审稿时长
>12 weeks
期刊介绍: The field of cellular and molecular bioengineering seeks to understand, so that we may ultimately control, the mechanical, chemical, and electrical processes of the cell. A key challenge in improving human health is to understand how cellular behavior arises from molecular-level interactions. CMBE, an official journal of the Biomedical Engineering Society, publishes original research and review papers in the following seven general areas: Molecular: DNA-protein/RNA-protein interactions, protein folding and function, protein-protein and receptor-ligand interactions, lipids, polysaccharides, molecular motors, and the biophysics of macromolecules that function as therapeutics or engineered matrices, for example. Cellular: Studies of how cells sense physicochemical events surrounding and within cells, and how cells transduce these events into biological responses. Specific cell processes of interest include cell growth, differentiation, migration, signal transduction, protein secretion and transport, gene expression and regulation, and cell-matrix interactions. Mechanobiology: The mechanical properties of cells and biomolecules, cellular/molecular force generation and adhesion, the response of cells to their mechanical microenvironment, and mechanotransduction in response to various physical forces such as fluid shear stress. Nanomedicine: The engineering of nanoparticles for advanced drug delivery and molecular imaging applications, with particular focus on the interaction of such particles with living cells. Also, the application of nanostructured materials to control the behavior of cells and biomolecules.
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