Donnenfield Jonah I, Proffen Benedikt L, Fleming Braden C, Murray Martha M
Division of Sports Medicine, Department of Orthopaedic Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Department of Orthopaedics, Warren Alpert Medical School of Brown University/Rhode Island Hospital, Providence, RI 02903, USA.
Bioengineering (Basel). 2023 Apr 26;10(5):527. doi: 10.3390/bioengineering10050527.
The relationship between cartilage and synovium is a rapidly growing area of osteoarthritis research. However, to the best of our knowledge, the relationships in gene expression between these two tissues have not been explored in mid-stage disease development. The current study compared the transcriptomes of these two tissues in a large animal model one year following posttraumatic osteoarthritis induction and multiple surgical treatment modalities. Thirty-six Yucatan minipigs underwent transection of the anterior cruciate ligament. Subjects were randomized to no further intervention, ligament reconstruction, or ligament repair augmented with an extracellular matrix (ECM) scaffold, followed by RNA sequencing of the articular cartilage and synovium at 52 weeks after harvest. Twelve intact contralateral knees served as controls. Across all treatment modalities, the primary difference in the transcriptomes was that the articular cartilage had greater upregulation of genes related to immune activation compared to the synovium-once baseline differences between cartilage and synovium were adjusted for. Oppositely, synovium featured greater upregulation of genes related to Wnt signaling compared to articular cartilage. After adjusting for expression differences between cartilage and synovium seen following ligament reconstruction, ligament repair with an ECM scaffold upregulated pathways related to ion homeostasis, tissue remodeling, and collagen catabolism in cartilage relative to synovium. These findings implicate inflammatory pathways within cartilage in the mid-stage development of posttraumatic osteoarthritis, independent of surgical treatment. Moreover, use of an ECM scaffold may exert a chondroprotective effect over gold-standard reconstruction through preferentially activating ion homeostatic and tissue remodeling pathways within cartilage.
软骨与滑膜之间的关系是骨关节炎研究中一个快速发展的领域。然而,据我们所知,在疾病发展中期,尚未对这两种组织之间的基因表达关系进行探索。本研究在创伤后骨关节炎诱导及多种手术治疗方式一年后的大型动物模型中,比较了这两种组织的转录组。三十六只尤卡坦小型猪接受了前交叉韧带横断术。将研究对象随机分为不进行进一步干预、韧带重建或用细胞外基质(ECM)支架增强韧带修复三组,随后在取材后52周对关节软骨和滑膜进行RNA测序。十二只完整的对侧膝关节作为对照。在所有治疗方式中,转录组的主要差异在于,在调整了软骨和滑膜之间的基线差异后,与滑膜相比,关节软骨中与免疫激活相关的基因上调更为明显。相反,与关节软骨相比,滑膜中与Wnt信号相关的基因上调更为明显。在调整韧带重建后软骨和滑膜之间的表达差异后,相对于滑膜,用ECM支架进行韧带修复可上调软骨中与离子稳态、组织重塑和胶原分解代谢相关的通路。这些发现表明,在创伤后骨关节炎的中期发展中,软骨内的炎症通路发挥作用,且与手术治疗无关。此外,使用ECM支架可能通过优先激活软骨内的离子稳态和组织重塑通路,对金标准重建发挥软骨保护作用。