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髋关节股骨髋臼撞击症治疗过程中收获的软骨细胞的活力。

Viability of chondrocytes harvested during treatment of hip femoroacetabular impingement.

作者信息

DeFroda Steven, Jones Molly, Rigden Bryce, Bischoff Caleb, Richards Jarod, Crist Brett, Stoker Aaron, Cook James

机构信息

University of Missouri- Columbia School of Medicine, Columbia, USA.

Thompson Laboratory for Regenerative Orthopaedics, University of Missouri, Columbia, USA.

出版信息

Arch Orthop Trauma Surg. 2025 Jun 7;145(1):336. doi: 10.1007/s00402-025-05953-2.

Abstract

PURPOSE

This study aimed to collect tissue overlying a CAM deformity for subsequent cell culture and chondrocyte expression as a proof of concept of clinical feasibility for autologous cell-based cartilage restoration in the hip.

METHODS

IRB approval was obtained to collect otherwise-discarded tissues from patients undergoing surgical management of labral tears and FAI. The collected tissue was exposed to collagenase type II for 16-24 h for chondrocyte isolation. Isolated cells were counted and seeded onto T-25 flasks in DMEM supplemented with 10% FBS. Media was changed every three days until > 90% confluency. At confluency, cells were counted and seeded onto a T-175 flask representing passage one. At second confluency, cells were counted again; if the total did not surpass 20,000,000 cells based on the minimum number needed for cell-based treatments, they were seeded onto two T-175 flasks representing passage two. Cells were not expanded beyond passage two based on the goal of phenotype maintenance.

RESULTS

Mean weight of collected tissues was 209.69 ± 78.09 mg (median = 202 mg). 41 of 55 samples reached > 20,000,000 cells at a mean of 33.98 ± 13.06 days (median = 30 days). Mean initial cell seeding of successful expansions was 1,116,871.79 ± 2,271,995.77 cells (median = 340,000 cells). Of samples that failed to reach threshold, five did not have sufficient cells following chondrocyte isolation to establish culture, and nine did not progress toward confluency for passage one. There were no significant differences in patient age (p =.988) or sex (p =.537) between successful versus unsuccessful expansions. There was a significant difference in patient BMI (p <.001) between successful versus unsuccessful expansions.

CONCLUSIONS

74.5% of tissue samples reached the minimum threshold (20 million cells), indicating successful expansions that may be sufficient for use in hip preservation procedures involving cell-based cartilage restoration. These findings support the viability of chondrocytes harvested from tissue overlying CAM deformities, and the feasibility of utilizing the tissue in subsequent autologous chondrocyte implantation procedures.

摘要

目的

本研究旨在收集凸轮畸形(CAM)上方的组织,用于后续的细胞培养和软骨细胞表达,以证明基于自体细胞的髋关节软骨修复临床可行性的概念验证。

方法

获得机构审查委员会(IRB)批准,从接受髋臼唇撕裂和股骨髋臼撞击症(FAI)手术治疗的患者中收集原本会被丢弃的组织。将收集到的组织暴露于II型胶原酶中16 - 24小时以分离软骨细胞。对分离出的细胞进行计数,并接种到补充有10%胎牛血清(FBS)的DMEM培养基的T - 25培养瓶中。每三天更换一次培养基,直到细胞汇合度超过90%。在汇合时,对细胞进行计数并接种到代表第1代的T - 175培养瓶中。在第二次汇合时,再次对细胞进行计数;如果总数未超过基于细胞治疗所需的最小数量20,000,000个细胞,则将它们接种到代表第2代的两个T - 175培养瓶中。基于维持细胞表型的目标,细胞传代不超过第2代。

结果

收集到的组织平均重量为209.69±78.09毫克(中位数 = 202毫克)。55个样本中有41个在平均33.98±13.06天(中位数 = 30天)时达到超过20,000,000个细胞。成功扩增的平均初始细胞接种数为1,116,871.79±2,271,995.77个细胞(中位数 = 340,000个细胞)。在未达到阈值的样本中,5个在软骨细胞分离后没有足够的细胞来建立培养,9个在第1代培养过程中未达到汇合。成功与未成功扩增的患者年龄(p = 0.988)或性别(p = 0.537)无显著差异。成功与未成功扩增的患者体重指数(BMI)存在显著差异(p < 0.001)。

结论

74.5%的组织样本达到了最小阈值(2000万个细胞),表明成功扩增,这可能足以用于涉及基于细胞的软骨修复的髋关节保留手术。这些发现支持了从凸轮畸形上方组织收获软骨细胞的可行性,以及在后续自体软骨细胞植入手术中利用该组织的可行性。

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