Identification of a Regenerative Protocol for Recellularizing Human Auricular Cartilage Scaffolds.

IF 1.4 4区 医学 Q3 SURGERY Annals of Plastic Surgery Pub Date : 2024-11-01 DOI:10.1097/SAP.0000000000004137
Mary E Ziegler, Leonardo Alaniz, Nawal Khan, Melinda Lem, Jason Pham, Arya Sherafat, Jacklyn Melkonian, Nikhil Prabhakar, Madelyn Shay, Kadir B Oyur, Miles J Pfaff, Alan D Widgerow
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Abstract

Objective: Utilizing biological scaffolds for cartilage tissue engineering is a promising tool for improving auricular reconstruction. Decellularized auricular scaffolds provide a means of regenerating cartilage for in vivo implantation, but identifying the ideal regenerative mix remains challenging.

Methods: Human cadaver auricular cartilage was decellularized and recellularized with either auricular chondrocytes alone, auricular chondrocytes with adipose-derived stem cells, or both cells with platelet-rich plasma. Confirmation of decellularization and recellularization was done by hematoxylin and eosin staining. Extracellular matrix preservation and production were determined by Masson's trichrome, Alcian blue, and Verhoeff-van Gieson staining. Collagen II assessments were made using immunohistochemistry.

Results: Decellularization of cadaver auricular cartilage was confirmed by the absence of cells, reduction in glycosaminoglycans, and the preservation of collagen and elastin. Recellularization was more efficient when chondrocytes were seeded with adipose-derived stem cells, which was enhanced by adding platelet-rich plasma. Coculture with platelet-rich plasma yielded better total collagen (56% increase) and glycosaminoglycan (47% increase) induction. Moreover, when platelet-rich plasma was added, collagen II induction was significantly increased (42%; P < 0.05).

Conclusion: We identified a regenerative protocol that included auricular chondrocytes, adipose-derived stem cells, and platelet-rich plasma, which stimulated chondrogenesis on decellularized auricular cartilage. This finding provides a model to explore cartilage formation and the potential for improving auricular and cartilage-based reconstruction.

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确定人耳廓软骨支架再细胞化的再生方案。
目的:利用生物支架进行软骨组织工程是改善耳廓重建的有效手段。方法:对人体尸体耳廓软骨进行脱细胞处理,然后用单独的耳廓软骨细胞、耳廓软骨细胞与脂肪来源干细胞或两种细胞与富血小板血浆进行再细胞化。脱细胞和再细胞化的确认是通过苏木精和伊红染色完成的。细胞外基质的保存和生成是通过马森三色染色法、阿尔西安蓝染色法和Verhoeff-van Gieson染色法确定的。使用免疫组化方法对胶原蛋白II进行评估:结果:尸体耳廓软骨的脱细胞化通过细胞的缺失、糖胺聚糖的减少以及胶原蛋白和弹性蛋白的保留得到了证实。当软骨细胞与脂肪来源的干细胞一起播种时,再细胞化的效率更高,加入富血小板血浆后,再细胞化的效率更高。与富血小板血浆共培养能更好地诱导总胶原蛋白(增加56%)和糖胺聚糖(增加47%)。此外,加入富血小板血浆后,胶原蛋白II的诱导率显著增加(42%;P < 0.05):我们确定了一种包括耳软骨细胞、脂肪来源干细胞和富血小板血浆的再生方案,它能刺激脱细胞耳软骨上的软骨生成。这一发现提供了一个探索软骨形成的模型,以及改善耳廓和软骨重建的潜力。
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来源期刊
CiteScore
2.70
自引率
13.30%
发文量
584
审稿时长
6 months
期刊介绍: The only independent journal devoted to general plastic and reconstructive surgery, Annals of Plastic Surgery serves as a forum for current scientific and clinical advances in the field and a sounding board for ideas and perspectives on its future. The journal publishes peer-reviewed original articles, brief communications, case reports, and notes in all areas of interest to the practicing plastic surgeon. There are also historical and current reviews, descriptions of surgical technique, and lively editorials and letters to the editor.
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