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硫酸乙酰肝素 6-O 内切酶在椎间盘稳态中的作用。

Role of heparan sulfate 6-0 endosulfatases in intervertebral disc homeostasis.

机构信息

Department of Orthopedic Surgery, Osaka Medical College, Japan.

Department of Molecular Medicine, The Scripps Research Institute, USA.

出版信息

Histol Histopathol. 2019 Sep;34(9):1051-1060. doi: 10.14670/HH-18-107. Epub 2019 Mar 29.

Abstract

The expression of heparan sulfate endosulfatases (Sulfs) was investigated in the intervertebral disc (IVD) to clarify their role in IVD homeostasis. Sulf-1 and -2 expression were elucidated in normal and degenerated human IVD. Age-related effects on Sulf expression, type II collagen levels, and structural changes were analyzed in IVDs of wild-type (WT) and Sulf-1 knockout (Sulf-1⁻/⁻) mice. The effect of recombinant Sulf-1 (100 ng/ml) and Sulf-1 knockdown on heparan sulfate proteoglycan and collagen expression in ATDC5 cells were examined. Finally, the effect of Sulf-1 on transforming growth factor (TGF) β1-induced signaling was evaluated. Results show that Sulf-1 and -2 levels were higher in degenerated human IVDs. In WT mice, Sulf-1 and -2 expression generally declined as the animals aged. In particular, Sulf-1 in the nucleus pulposus was higher compared with Sulf-2 at the age of 1 and 6 months and significantly declined with aging. Sulf-1⁻/⁻ mice showed more severe IVD pathology than WT mice, with lower type II collagen levels in nucleus pulposus, and degeneration with type I collagen in annulus fibrosus. In vitro, Sulf-1 induced type II collagen expression and significantly increased TGF-β1-induced Smad2/3 phosphorylation in ATDC5 cells. In conclusion, Sulf-1 might play a critical role from development to maintenance of IVD homeostasis by regulating collagen expression.

摘要

目的

探讨硫酸乙酰肝素内切酶(Sulfs)在椎间盘(IVD)中的表达,以阐明其在 IVD 稳态中的作用。

方法

阐明正常和退变人椎间盘内 Sulf-1 和 -2 的表达。分析野生型(WT)和 Sulf-1 敲除(Sulf-1⁻/⁻)小鼠椎间盘内 Sulf 表达、Ⅱ型胶原水平和结构变化的年龄相关性。检测重组 Sulf-1(100ng/ml)和 Sulf-1 敲低对 ATDC5 细胞中硫酸乙酰肝素蛋白聚糖和胶原表达的影响。最后,评估 Sulf-1 对转化生长因子(TGF)β1 诱导信号的影响。

结果

退变人椎间盘内 Sulf-1 和 -2 水平升高。在 WT 小鼠中,随着年龄的增长,Sulf-1 和 -2 的表达普遍下降。特别是,1 和 6 月龄时核髓内 Sulf-1 的表达高于 Sulf-2,随着年龄的增长显著下降。与 WT 小鼠相比,Sulf-1⁻/⁻小鼠的 IVD 病变更严重,核髓内Ⅱ型胶原水平较低,纤维环出现 I 型胶原退变。体外,Sulf-1 诱导Ⅱ型胶原表达,并显著增加 ATDC5 细胞中 TGF-β1 诱导的 Smad2/3 磷酸化。

结论

Sulf-1 可能通过调节胶原表达,从发育到维持 IVD 稳态中发挥关键作用。

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