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致密性骨发育不全患者的侵蚀性关节炎:一个自然实验。

Erosive arthritis in a patient with pycnodysostosis: an experiment of nature.

作者信息

Ainola Mari, Valleala Heikki, Nykänen Pekka, Risteli Juha, Hanemaaijer Roeland, Konttinen Yrjö T

机构信息

Helsinki University Central Hospital, Helsinki, Finland.

出版信息

Arthritis Rheum. 2008 Nov;58(11):3394-401. doi: 10.1002/art.23996.

Abstract

OBJECTIVE

The excellent poster painter Henri de Toulouse-Lautrec is the most famous patient with cathepsin K-deficient pycnodysostosis. Cathepsin K is believed to play a major role in osteoclast-driven bone resorption. In this study we explored the role of cathepsin K in bone resorption in a patient with a cathepsin K mutation causing pycnodysostosis in whom psoriatic arthritis also developed. We hypothesized that the patient would develop only inflammatory synovitis but would not develop bone erosions or other osteolytic changes.

METHODS

Monocytes from the patient with pycnodysostosis and normal control monocytes were isolated and stimulated to fuse and form multinuclear osteoclast-like cells, which were identified by evaluating messenger RNA expression of osteoclast markers. The ability to resorb bone was assessed by determining the extent of pit formation and levels of collagen degradation products generated by cathepsin K (C-terminal crosslinking telopeptide of type I collagen [CTX]) and matrix metalloproteinases (pyridinoline crosslinked C-terminal telopeptide of type I collagen). These experiments were also done in normal control cells after incubation with the cathepsin K inhibitor E64 during bone resorption.

RESULTS

In contrast to our a priori hypothesis, the patient developed a mutilating disease with extensive bony erosions associated with lysis of some of the distal phalanges of her hands and feet. After stimulation of monocytes from this patient, the cells formed multinuclear tartrate-resistant acid phosphatase-positive and calcitonin receptor-positive multikaryons, which, however, totally lacked cathepsin K. These multinuclear cells were able to resorb bone but, in contrast to normal control osteoclasts, did not produce CTX. The resorption pattern was abnormal in that, unlike normal control osteoclasts, both osteoclasts from the patient and E64-inhibited osteoclasts did not leave extensive osteoclast trails, but were relatively sessile.

CONCLUSION

In this "experiment of nature" we observed that cathepsin K is not necessary for bone degradation. These findings may be pertinent to our understanding of the functions of cathepsin K inhibitors, which are currently being developed as drugs to treat metabolic bone diseases.

摘要

目的

杰出的海报画家亨利·德·图卢兹-洛特雷克是患有组织蛋白酶K缺乏性致密性骨发育不全的最著名患者。组织蛋白酶K被认为在破骨细胞驱动的骨吸收中起主要作用。在本研究中,我们探讨了组织蛋白酶K在一名因组织蛋白酶K突变导致致密性骨发育不全且并发银屑病关节炎的患者的骨吸收中的作用。我们假设该患者只会发展为炎症性滑膜炎,而不会出现骨侵蚀或其他溶骨性改变。

方法

分离患有致密性骨发育不全患者的单核细胞和正常对照单核细胞,并刺激它们融合形成多核破骨细胞样细胞,通过评估破骨细胞标志物的信使核糖核酸表达来鉴定这些细胞。通过测定凹坑形成的程度以及组织蛋白酶K(I型胶原C末端交联端肽[CTX])和基质金属蛋白酶(I型胶原吡啶啉交联C末端端肽)产生的胶原降解产物水平来评估骨吸收能力。在骨吸收过程中,用组织蛋白酶K抑制剂E64孵育正常对照细胞后也进行了这些实验。

结果

与我们的先验假设相反,该患者发展为致残性疾病,伴有广泛的骨侵蚀,累及她手脚的一些远端指骨溶解。刺激该患者的单核细胞后,细胞形成了多核抗酒石酸酸性磷酸酶阳性和降钙素受体阳性的多核细胞,然而,这些细胞完全缺乏组织蛋白酶K。这些多核细胞能够吸收骨,但与正常对照破骨细胞不同的是,它们不产生CTX。吸收模式异常,与正常对照破骨细胞不同,该患者的破骨细胞和E64抑制的破骨细胞都没有留下广泛的破骨细胞痕迹,而是相对固定不动。

结论

在这个“自然实验”中,我们观察到组织蛋白酶K对于骨降解并非必需。这些发现可能与我们对组织蛋白酶K抑制剂功能的理解相关,目前组织蛋白酶K抑制剂正作为治疗代谢性骨病的药物进行研发。

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