Department of Plastic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Stem Cells Dev. 2022 Oct;31(19-20):621-629. doi: 10.1089/scd.2021.0355. Epub 2022 May 25.
Adipose therapeutics, including isolated cell fractions and tissue emulsifications, have been explored for osteoarthritis (OA) treatment; however, the optimal preparation method and bioactive tissue component for healing has yet to be determined. This in vitro study compared the effects of adipose preparations on cultured knee chondrocytes. De-identified human articular chondrocytes were co-cultured with adipose preparations for 36 or 72 h. Human adipose tissues were obtained from abdominal panniculectomy procedures and processed using three different techniques: enzymatic digestion to release stromal vascular fraction (SVF), emulsification with luer-to-luer transfer (nanofat), and processing in a bead-mill (Lipogems, Lipogems International SpA, Milan, Italy). Gene expression in both chondrocytes and adipose preparations was measured to assess cellular inflammation, catabolism, and anabolism. Results demonstrated that chondrocytes cultured with SVF consistently showed increased inflammatory and catabolic gene expression compared with control chondrocytes at both 36- and 72-h timepoints. Alternatively, chondrocytes co-cultured with either nanofat or bead-mill processed adipose derivatives yielded minimal pro-inflammatory effects and instead increased anabolism and regeneration of cartilage extracellular matrix. Interestingly, nanofat preparations induced transient matrix anabolism while Lipogems adipose consistently demonstrated increased matrix synthesis at both study timepoints after co-culture. This evaluation of the regenerative potential of adipose-derived preparations as a clinical tool for knee OA treatment suggests that mechanically processed preparations may be more efficacious than an isolated SVF cell preparation.
脂肪治疗学,包括分离的细胞成分和组织乳化液,已被探索用于骨关节炎(OA)的治疗;然而,对于愈合而言,最佳的制备方法和生物活性组织成分仍有待确定。本体外研究比较了脂肪制剂对培养的膝关节软骨细胞的影响。分离的人关节软骨细胞与脂肪制剂共培养 36 或 72 小时。从腹部脂肪切除术获得人脂肪组织,并使用三种不同的技术进行处理:酶消化以释放基质血管部分(SVF)、用鲁尔到鲁尔转移(纳米脂肪)乳化和在珠磨机中处理(Lipogems,Lipogems International SpA,米兰,意大利)。测量软骨细胞和脂肪制剂中的基因表达,以评估细胞炎症、分解代谢和合成代谢。结果表明,与对照软骨细胞相比,SVF 培养的软骨细胞在 36 和 72 小时两个时间点均显示出持续增加的炎症和分解代谢基因表达。相反,与纳米脂肪或珠磨处理的脂肪衍生制剂共培养的软骨细胞产生的促炎作用最小,反而增加了软骨细胞外基质的合成代谢和再生。有趣的是,纳米脂肪制剂诱导了短暂的基质合成代谢,而 Lipogems 脂肪在共培养后两个研究时间点均持续显示出增加的基质合成。对脂肪衍生制剂作为膝骨关节炎治疗的临床工具的再生潜力的评估表明,机械处理的制剂可能比分离的 SVF 细胞制剂更有效。