Bergstrom Annika R, Glimm Matthew G, Houske Eden A, Cooper Gwendolyn, Viles Ethan, Chapman Marrin, Bourekis Katherine, Welhaven Hope D, Brahmachary Priyanka P, Hahn Alyssa K, June Ronald K
Department of Biological & Environmental Science, Carroll College, Helena, MT, USA, 59625.
Department of Chemical & Biological Engineering, Villanova University, Villanova, PA, USA, 19085.
bioRxiv. 2024 Jul 4:2024.07.01.601604. doi: 10.1101/2024.07.01.601604.
The mechanism by which chondrocytes respond to reduced mechanical loading environments and the subsequent risk of developing osteoarthritis remains unclear. This is of particular concern for astronauts. In space the reduced joint loading forces during prolonged microgravity (10 ) exposure could lead to osteoarthritis (OA), compromising quality of life post-spaceflight. In this study, we encapsulated human chondrocytes in an agarose gel of similar stiffness to the pericellular matrix to mimic the cartilage microenvironment. We then exposed agarose-chondrocyte constructs to simulated microgravity (SM) using a rotating wall vessel (RWV) bioreactor to better assess the cartilage health risks associated with spaceflight. Global metabolomic profiling detected a total of 1205 metabolite features across all samples, with 497 significant metabolite features identified by ANOVA (FDR-corrected p-value < 0.05). Specific metabolic shifts detected in response to SM exposure resulted in clusters of co-regulated metabolites, as well as key metabolites identified by variable importance in projection scores. Microgravity-induced metabolic shifts in gel constructs and media were indicative of protein synthesis, energy metabolism, nucleotide metabolism, and oxidative catabolism. The microgravity associated-metabolic shifts were consistent with early osteoarthritic metabolomic profiles in human synovial fluid, which suggests that even short-term exposure to microgravity (or other reduced mechanical loading environments) may lead to the development of OA.
软骨细胞对机械负荷降低环境的反应机制以及随后发生骨关节炎的风险仍不清楚。这对宇航员来说尤为重要。在太空中,长时间微重力(10)暴露期间关节负荷力降低可能导致骨关节炎(OA),影响太空飞行后的生活质量。在本研究中,我们将人软骨细胞封装在与细胞周围基质硬度相似的琼脂糖凝胶中,以模拟软骨微环境。然后,我们使用旋转壁式生物反应器(RWV)将琼脂糖-软骨细胞构建体暴露于模拟微重力(SM)下,以更好地评估与太空飞行相关的软骨健康风险。全局代谢组学分析在所有样本中总共检测到1205个代谢物特征,通过方差分析(FDR校正p值<0.05)鉴定出497个显著代谢物特征。响应SM暴露检测到的特定代谢变化导致共调节代谢物簇以及通过投影得分中的变量重要性鉴定的关键代谢物。凝胶构建体和培养基中微重力诱导的代谢变化表明蛋白质合成、能量代谢、核苷酸代谢和氧化分解代谢。与微重力相关的代谢变化与人类滑液中的早期骨关节炎代谢组学特征一致,这表明即使短期暴露于微重力(或其他机械负荷降低的环境)也可能导致OA的发生。