Department of Orthopaedic Surgery, Center for Cellular and Molecular Engineering, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
McGowan Institute for Regenerative Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
FASEB J. 2021 Mar;35(3):e21410. doi: 10.1096/fj.202002386R.
Autologous chondrocyte implantation (ACI) is a regenerative procedure used to treat focal articular cartilage defects in knee joints. However, age has been considered as a limiting factor and ACI is not recommended for patients older than 40-50 years of age. One reason for this may be due to the reduced capacity of aged chondrocytes in generating new cartilage. Currently, the underlying mechanism contributing to aging-associated functional decline in chondrocytes is not clear and no proven approach exists to reverse chondrocyte aging. Given that chondrocytes in healthy hyaline cartilage typically display a spherical shape, believed to be essential for chondrocyte phenotype stability, we hypothesize that maintaining aged chondrocytes in a suspension culture that forces the cells to adopt a round morphology may help to "rejuvenate" them to a younger state, thus, leading to enhanced cartilage regeneration. Chondrocytes isolated from aged donors displayed reduced proliferation potential and impaired capacity in generating hyaline cartilage, compared to cells isolated from young donors, indicated by increased hypertrophy and cellular senescence. To test our hypothesis, the "old" chondrocytes were seeded as a suspension onto an agarose-based substratum, where they maintained a round morphology. After the 3-day suspension culture, aged chondrocytes displayed enhanced replicative capacity, compared to those grown adherent to tissue culture plastic. Moreover, chondrocytes subjected to suspension culture formed new cartilage in vitro with higher quality and quantity, with enhanced cartilage matrix deposition, concomitant with lower levels of hypertrophy and cellular senescence markers. Mechanistic analysis suggested the involvement of the RhoA and ERK1/2 signaling pathways in the "rejuvenation" process. In summary, our study presents a robust and straightforward method to enhance the function of aged human chondrocytes, which can be conveniently used to generate a large number of high-quality chondrocytes for ACI application in the elderly.
自体软骨细胞移植(ACI)是一种用于治疗膝关节关节软骨缺损的再生程序。然而,年龄被认为是一个限制因素,ACI 不建议用于 40-50 岁以上的患者。原因之一可能是由于年龄较大的软骨细胞生成新软骨的能力降低。目前,导致软骨细胞与年龄相关的功能下降的潜在机制尚不清楚,也没有有效的方法来逆转软骨细胞衰老。鉴于健康透明软骨中的软骨细胞通常呈球形,这被认为是软骨细胞表型稳定的关键,我们假设将衰老的软骨细胞在悬浮培养中维持,迫使细胞采用圆形形态,可能有助于“使它们恢复年轻状态”,从而增强软骨再生。与年轻供体分离的细胞相比,来自老年供体的软骨细胞显示出增殖潜力降低和产生透明软骨的能力受损,这表现为肥大和细胞衰老增加。为了验证我们的假设,将“老”软骨细胞作为悬浮液接种在琼脂糖基基质上,使其保持圆形形态。经过 3 天的悬浮培养后,与贴壁培养的细胞相比,衰老的软骨细胞显示出增强的复制能力。此外,经过悬浮培养的软骨细胞在体外形成了具有更高质量和数量的新软骨,伴随着更高的软骨基质沉积,同时肥大和细胞衰老标志物水平降低。机制分析表明 RhoA 和 ERK1/2 信号通路参与了“年轻化”过程。总之,我们的研究提出了一种增强衰老人类软骨细胞功能的稳健而简单的方法,可方便地用于产生大量高质量的软骨细胞,用于老年人的 ACI 应用。