Posey Karen L, Coustry Francoise, Veerisetty Alka C, Liu Peiman, Alcorn Joseph L, Hecht Jacqueline T
Department of Pediatrics, University of Texas Medical School at Houston, TX, USA.
J Bone Miner Res. 2014;29(5):1258-68. doi: 10.1002/jbmr.2139.
Mutations in the gene encoding cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia (PSACH), a severe dwarfing condition. Pain, a significant complication, has generally been attributed to joint abnormalities and erosion and early onset osteoarthritis. Previously, we found that the inflammatory-related transcripts were elevated in growth plate and articular cartilages, indicating that inflammation plays an important role in the chondrocyte disease pathology and may contribute to the overall pain sequelae. Here, we describe the effects of D469-delCOMP expression on the skeleton and growth plate chondrocytes with the aim to define a treatment window and thereby reduce pain. Consistent with the human PSACH phenotype, skeletal development of D469del-COMP mice was normal and similar to controls at birth. By postnatal day 7 (P7), the D469del-COMP skeleton, limbs, skull and snout were reduced and this reduction was progressive during postnatal growth, resulting in a short-limbed dwarfed mouse. Modulation of prenatal and postnatal expression of D469del-COMP showed minimal retention/cell death at P7 with some retention/cell death by P14, suggesting that earlier treatment intervention at the time of PSACH diagnosis may produce optimal results. Important and novel findings were an increase in inflammatory proteins generally starting at P21 and that exercise exacerbates inflammation. These observations suggest that pain in PSACH may be related to an intrinsic inflammatory process that can be treated symptomatically and is not related to early joint erosion. We also show that genetic ablation of CHOP dampens the inflammatory response observed in mice expressing D469del-COMP. Toward identifying potential treatments, drugs known to decrease cellular stress (lithium, phenylbutyric acid, and valproate) were assessed. Interestingly, all diminished the chondrocyte pathology but had untoward outcomes on mouse growth, development, and longevity. Collectively, these results define an early treatment window in which chondrocytes can be salvaged, thereby potentially increasing skeletal growth and decreasing pain.
编码软骨寡聚基质蛋白(COMP)的基因突变会导致假性软骨发育不全(PSACH),这是一种严重的侏儒症。疼痛是一种显著的并发症,通常被认为是由关节异常、侵蚀以及早期骨关节炎引起的。此前,我们发现生长板和关节软骨中与炎症相关的转录本水平升高,这表明炎症在软骨细胞疾病病理学中起重要作用,并且可能导致整体疼痛后遗症。在此,我们描述了D469-delCOMP表达对骨骼和生长板软骨细胞的影响,旨在确定一个治疗窗口期,从而减轻疼痛。与人类PSACH表型一致,D469del-COMP小鼠出生时骨骼发育正常,与对照组相似。到出生后第7天(P7),D469del-COMP小鼠的骨骼、四肢、头骨和口鼻部尺寸减小,且这种减小在出生后生长过程中持续进展,导致小鼠出现短肢侏儒症。对D469del-COMP产前和产后表达的调节显示,P7时细胞保留/死亡最少,到P14时出现一些细胞保留/死亡,这表明在PSACH诊断时更早进行治疗干预可能会产生最佳效果。重要且新颖的发现是,炎症蛋白通常从P21开始增加,并且运动加剧炎症。这些观察结果表明,PSACH中的疼痛可能与一种内在炎症过程有关,这种炎症可以通过对症治疗,且与早期关节侵蚀无关。我们还表明,CHOP基因敲除可减轻在表达D469del-COMP的小鼠中观察到的炎症反应。为了确定潜在的治疗方法,我们评估了已知可减轻细胞应激的药物(锂盐、苯丁酸钠和丙戊酸盐)。有趣的是,所有这些药物都减轻了软骨细胞病理学改变,但对小鼠的生长、发育和寿命产生了不良影响。总体而言,这些结果确定了一个早期治疗窗口期,在此期间软骨细胞可以得到挽救,从而有可能促进骨骼生长并减轻疼痛。