地塞米松和 IGF-1 对太空中人体软骨-骨-滑膜微生理系统创伤后骨关节炎样分解代谢变化和地球上地面控制组织的影响

Garima Dwivedi, Lisa Flaman, Begum Alaybeyoglu, E. Frank, R. M. Black, J. Fite, Chris Scherzer, Ken Barton, Elizabeth Luyster, Nathan Thomas, Eugene Boland, Yamini Krishnan, H. Hung, Susan Chubinskaya, S. Trippel, E. Geishecker, Vicki Rosen, Patrik Önnerfjord, Murat Cirit, A. Grodzinsky
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引用次数: 0

摘要

创伤后骨关节炎(PTOA)源于创伤性关节损伤(如前交叉韧带断裂)。机械冲击和滑膜炎症反应可导致关节组织退化,并在较长时间内发展为创伤后骨关节炎。宇航员容易受到更多与运动相关的关节损伤,导致肌肉骨骼生理学改变,而微重力和电离辐射暴露的增加又进一步加剧了这种损伤。我们采用人类软骨-骨-合成细胞(CBS)共培养模型来测试低剂量地塞米松(Dex)和 IGF-1 在改善地球和国际空间站-国家实验室(ISS-NL,简称 ISS)上类似 PTOA 退化的潜力。CBS 共培养是利用骨软骨栓(CB)受挤压冲击损伤(INJ)后与滑膜(S)外植体共培养建立的。研究组包括对照组(CB)、疾病组[CBS + INJ]、治疗组[CBS + INJ + Dex + IGF-1]和药物安全组[CB + Dex + IGF-1]。结果测量包括细胞存活率、基质糖胺聚糖(GAG)和胶原的改变、释放细胞因子的多重-ELISA定量、组织病理学以及废培养基的代谢组学和蛋白质组学分析。在国际空间站(ISS-NL)上进行的一项为期 21 天的研究探讨了类似 PTOA 的发病机制和微重力下的治疗方法。研究小组的组织卡在多用途可变g平台(MVP)内的定制培养室中进行培养。在太空中的 CBS + INJ 组和使用相同供体组织的地面对照组中,观察到炎症细胞因子释放明显上调和组织-GAG 损失,这与之前在地球上进行的多供体研究中报告的情况类似;这些变化在一定程度上被 Dex + IGF-1 所改善,但供体存在差异。代谢组学和蛋白质组学分析表明,在太空与在地球上释放到培养基中的代谢物/蛋白质之间存在一系列明显差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of dexamethasone and IGF-1 on post-traumatic osteoarthritis-like catabolic changes in a human cartilage-bone-synovium microphysiological system in space and ground control tissues on earth
Post-traumatic Osteoarthritis (PTOA) results from traumatic joint injuries (such as an ACL rupture). Mechanical impact and an immediate synovial inflammatory response can result in joint tissue degradation and longer-term progression to PTOA. Astronauts are susceptible to increased exercise-related joint injuries leading to altered musculoskeletal physiology, further escalated due to microgravity and increased exposure to ionizing radiation. We applied a human Cartilage-Bone-Synovium (CBS) coculture model to test the potential of low-dose dexamethasone (Dex) and IGF-1 in ameliorating PTOA-like degeneration on Earth and the International Space Station-National Laboratory (ISS-NL, ISS for short). CBS cocultures were established using osteochondral plugs (CB) subjected to compressive impact injury (INJ) followed by coculture with synovium (S) explants. Study groups consisted of control (CB); disease [CBS + INJ]; treatment [CBS + INJ + Dex + IGF-1]; and drug-safety [CB + Dex + IGF-1]. Outcome measures included cell viability, altered matrix glycosaminoglycans (GAG) and collagens, multiplex-ELISA quantification of released cytokines, histopathology, and metabolomic and proteomic analyses of spent media. A 21-day study on ISS-NL explored PTOA-like pathogenesis and treatment in microgravity. Tissue cards for study groups were cultured in custom-built culture chambers within multi-use variable-g platforms (MVPs). A marked upregulation in the release of inflammatory cytokines and tissue-GAG loss was observed in CBS + INJ groups in space and ground controls utilizing tissues from the same donors, similar to that reported in a previous multi-donor study on Earth; these changes were partly ameliorated by Dex + IGF-1, but with donor variability. Metabolomic and proteomic analyses revealed an array of distinct differences between metabolites/proteins released to the medium in Space versus on Earth.
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