Cathepsin K Localizes to Equine Bone In Vivo and Inhibits Bone Marrow Stem and Progenitor Cells Differentiation In Vitro.

IF 1.1 Q4 CELL & TISSUE ENGINEERING Journal of Stem Cells & Regenerative Medicine Pub Date : 2017-12-18 eCollection Date: 2017-01-01
Hayam Hussein, Prosper Boyaka, Jennifer Dulin, Duncan Russell, Lauren Smanik, Mohamed Azab, Alicia L Bertone
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Abstract

Selective inhibition of Cathepsin K (CatK) has a promising therapeutic potential for diseases associated with bone loss and osseous inflammation, such as osteoarthritis, periodontitis, and osteoporosis. In horses, stress-related bone injuries are common and accompanied by bone pain and inflammation resulting in excessive bone resorption and periostitis. VEL-0230 is a highly selective inhibitor of CatK that significantly decreased bone resorption and increased bone formation biomarkers. The goal of this study was to demonstrate the presence of CatK in equine bone and a simultaneous influence on the bone marrow cellular components including function and differentiation. Our objectives were: 1) to investigate the tissue localization of CatK protein in equine bone using immunohistochemistry, and 2) to determine the effect of CatK inhibition on osteoclastogenic, chondrogenic and osteogenic differentiation potential of equine stem and progenitor cells in vitro using histochemical staining and differentiation-related gene expression analyses. Bone biopsies, harvested from the tuber coxae and proximal phalanx of six healthy horses, were processed for immunostaining against CatK. Sternal bone marrow aspirates were cultured in 0, 1, 10, or 100 μM of VEL-0230 and subsequent staining scoring and gene expression analyses performed. All cells morphologically characterized as osteoclasts and moderate number of active bone lining osteoblasts stained positive for CatK. Histochemical staining and gene expression analyses revealed a significant increase in the osteoclastogenic, chondrogenic and osteogenic differentiation potential of equine bone marrow cells, which was VEL-0230-concentration dependent for the latter two. These results suggested that CatK inhibition may have anabolic effects on bone and cartilage regeneration that may be explained as a feedback response to CatK depletion. In conclusion, the use of CatK inhibition to reduce inflammation and associated bone resorption in equine osseous disorders may offer advantages to other therapeutics that would require further study.

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Cathepsin K 在体内定位到马骨并抑制体外骨髓干细胞和祖细胞分化。
选择性抑制酪蛋白酶 K(CatK)对骨质流失和骨炎相关疾病(如骨关节炎、牙周炎和骨质疏松症)具有很好的治疗潜力。在马匹中,与应力相关的骨损伤很常见,并伴有骨痛和炎症,导致骨过度吸收和骨膜炎。VEL-0230 是一种高选择性 CatK 抑制剂,可显著减少骨吸收,增加骨形成生物标志物。本研究的目的是证明 CatK 存在于马的骨骼中,并同时影响骨髓细胞成分,包括功能和分化。我们的目标是1)使用免疫组织化学方法研究 CatK 蛋白在马骨中的组织定位;2)使用组织化学染色和分化相关基因表达分析确定 CatK 抑制对马干细胞和祖细胞体外破骨细胞生成、软骨生成和成骨分化潜能的影响。从六匹健康马的跗关节和近节指骨处采集骨活检样本,并对其进行 CatK 免疫染色处理。用 0、1、10 或 100 μM 的 VEL-0230 培养胸骨骨髓抽吸物,然后进行染色评分和基因表达分析。所有形态上被定性为破骨细胞的细胞和适量的活性骨内膜成骨细胞的 CatK 染色均呈阳性。组织化学染色和基因表达分析表明,马骨髓细胞的破骨细胞分化潜能、软骨分化潜能和成骨细胞分化潜能均有显著提高,其中后两者与 VEL-0230 浓度有关。这些结果表明,CatK 抑制可能会对骨和软骨再生产生同化作用,这可以解释为对 CatK 消耗的反馈反应。总之,使用 CatK 抑制剂来减少马骨病的炎症和相关骨吸收可能比其他疗法更有优势,这需要进一步研究。
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来源期刊
CiteScore
3.40
自引率
0.00%
发文量
5
审稿时长
14 weeks
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