Department of Pathology, College of Veterinary Medicine, University of Georgia, Athens, Georgia, United States of America.
Equine Care Group, Mazy, Gembloux, Belgium.
PLoS One. 2023 Jul 14;18(7):e0287740. doi: 10.1371/journal.pone.0287740. eCollection 2023.
Degenerative Suspensory Ligament Desmitis (DSLD) negatively impacts connective tissues in horses, which often leads to progressive chronic pain and lameness. DSLD has been shown to be a systemic disorder that affects multiple body systems, including tendons, sclerae, and the aorta. Currently, the diagnosis is confirmed by post mortem histological examination of a tendon or suspensory ligament. Histology reveals inappropriate accumulations of proteoglycans in the tendons and other tissues in DSLD-affected horses. Unfortunately, there is no reliable method to diagnose DSLD in living horses. Recently, bone morphogenetic protein 2 (BMP2) was identified in active DSLD lesions. In addition, recent data from RNA sequencing (RNA-seq) showed overexpression of numerous genes, among them BMP2, FOS and genes for keratins in DSLD skin biopsies-derived RNA. We hypothesized that some of these genes can be used as biomarkers for diagnosis of DSLD in a panel. Overexpression of some of them was verified in quantitative real time PCR. Immunohistochemistry and RNAscope in-situ hybridization (ISH) assays were used to determine the level of overexpression of specific genes in skin biopsies from control and DSLD-affected horses. The RNAscope ISH assay has shown to be more reliable and more specific that immunohistochemistry. ISH confirmed a significant increase in KRT83 and BMP-2 in hair follicles in DSLD cases, as well as abnormally high expression of FOS in the epidermis, especially in aging horses. Because statistically relevant specificity and sensitivity was documented only for FOS and BMP2, but not KRT83 we recommend the use of FOS and BMP2 panel to diagnose DSLD. We conclude that a panel of two markers from the studied group (BMP2 and FOS) can serve as an additional diagnostic tool for DSLD in living horses, especially in older animals. Further studies are necessary to confirm if this biomarker panel could be used as a prospective tool to identify DSLD in horses as they age.
退行性悬韧带松解症(DSLD)会对马的结缔组织造成负面影响,这通常会导致进行性慢性疼痛和跛行。DSLD 已被证明是一种全身性疾病,会影响包括肌腱、巩膜和主动脉在内的多个身体系统。目前,该病的诊断通过对肌腱或悬韧带进行死后组织学检查来确认。组织学显示,DSLD 受影响的马的肌腱和其他组织中存在不适当的蛋白聚糖积累。不幸的是,目前尚无可靠的方法来诊断活马的 DSLD。最近,骨形态发生蛋白 2(BMP2)在活动性 DSLD 病变中被鉴定出来。此外,最近的 RNA 测序(RNA-seq)数据显示,大量基因表达过度,其中包括 BMP2、FOS 和 DSLD 皮肤活检衍生 RNA 中的角蛋白基因。我们假设其中一些基因可以作为该组的生物标志物用于诊断 DSLD。在定量实时 PCR 中验证了其中一些基因的过表达。免疫组织化学和 RNAscope 原位杂交(ISH)检测用于确定对照和 DSLD 受影响的马皮肤活检中特定基因的过表达水平。RNAscope ISH 检测比免疫组织化学更可靠、更具特异性。ISH 证实,在 DSLD 病例的毛囊中 KRT83 和 BMP-2 显著增加,表皮中 FOS 异常高表达,尤其是在老年马中。由于仅记录了 FOS 和 BMP2 的统计上相关的特异性和敏感性,而不是 KRT83,因此我们建议使用 FOS 和 BMP2 面板来诊断 DSLD。我们得出结论,来自研究组的两个标记物(BMP2 和 FOS)的标志物组合可作为活马 DSLD 的附加诊断工具,尤其是在老年动物中。需要进一步的研究来确认这个生物标志物组合是否可以作为识别马随着年龄增长而患 DSLD 的前瞻性工具。