Wan-Chiew Ng, Baki Marina Mat, Lokanathan Yogeswaran, Fauzi Mohd Busra, Azman Mawaddah
Department of Otorhinolaryngology-Head and Neck Surgery, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Department of Otorhinolaryngology-Head and Neck Surgery, Hospital Canselor Tuanku Muhriz, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Front Cell Dev Biol. 2024 Dec 5;12:1489901. doi: 10.3389/fcell.2024.1489901. eCollection 2024.
Approaches to regenerate vocal fold in glottic insufficiency remains to be a focus for exploration. This is attributed to the applications of cells or biological molecules alone result in fast degradation and inadequate for regeneration. Development of an injectable hydrogel for glottic insufficiency is challenging, as it needs to be non-cytotoxic, elastic yet possess good strength and easy to fabricate. This gap prompts us to study the feasibility of our genipin(gn)-crosslinked gelatin (G) hydrogel in encapsulating Wharton's Jelly Mesenchymal Stem Cells (WJMSCs) and basic fibroblast growth factor (bFGF) WJMSCs with the aim to provide regeneration in glottic insufficiency. WJMSCs was encapsulated into two optimised formulations with the density of 2,000,000 cells/mL. The encapsulated cells were tested for its morphology, cell viability, proliferation and migration. Then, the incorporation of basic fibroblast growth factor (bFGF) was done into a final formulation and was tested for the cellular response and inflammation. 6G 0.4gn demonstrated better cell viability after culturing for 7 day. After incorporation of bFGF into cell-laden 6G 0.4gn, encapsulated WJMSCs showed to have improved viability and migration. The inflammatory profile of the hydrogel was imperceptible and was regarded as minimal or no pro- and anti-inflammation. Altogether, we have first formulated 6G 0.4gn which is suitable to encapsulate WJMSCs and incorporation of bFGF. Current study fulfils the market need in vocal fold regeneration, by suggesting its rejuvenating potential in glottic insufficiency, yet this combined formulation should be studied further to justify its translation to clinical setting.
声门功能不全时声带再生的方法仍是一个探索重点。这是因为单独应用细胞或生物分子会导致快速降解且不足以实现再生。开发用于声门功能不全的可注射水凝胶具有挑战性,因为它需要无细胞毒性、有弹性且具有良好强度且易于制备。这一差距促使我们研究京尼平(gn)交联明胶(G)水凝胶包裹沃顿胶间充质干细胞(WJMSCs)和碱性成纤维细胞生长因子(bFGF)WJMSCs的可行性,旨在实现声门功能不全的再生。将WJMSCs包裹于两种优化配方中,细胞密度为2,000,000个细胞/毫升。对包裹的细胞进行形态、细胞活力、增殖和迁移测试。然后,将碱性成纤维细胞生长因子(bFGF)加入最终配方中,并测试细胞反应和炎症情况。6G 0.4gn在培养7天后显示出更好的细胞活力。将bFGF加入载有细胞的6G 0.4gn后,包裹的WJMSCs显示出活力和迁移能力得到改善。水凝胶的炎症特征不明显,被认为具有最小或无促炎和抗炎作用。总之,我们首次配制了适合包裹WJMSCs并加入bFGF的6G 0.4gn。当前研究通过表明其在声门功能不全中的恢复潜力满足了声带再生的市场需求,但这种联合配方应进一步研究以证明其向临床应用转化的合理性。