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Inhibition of rheumatoid arthritis by blocking connective tissue growth factor 被引量:4
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作者 Kazuhisa Nozawa Maki Fujishiro +1 位作者 Yoshinari Takasaki Iwao Sekigawa 《World Journal of Orthopedics》 2014年第5期653-659,共7页
The pathogenesis of rheumatoid arthritis(RA) remains to be completely elucidated so far; however, it is known that proinflammatory cytokines play a pivotal role in the induction of RA. Tumor necrosis factor(TNF-α), i... The pathogenesis of rheumatoid arthritis(RA) remains to be completely elucidated so far; however, it is known that proinflammatory cytokines play a pivotal role in the induction of RA. Tumor necrosis factor(TNF-α), in particular, is considered to play a central role in bone destruction by mediating the abnormal activation of osteoclasts or the production of proteolytic enzymes through direct or indirect mechanisms. The use of TNF-α blocking agents has a significant impact on RA therapy. Anti-TNF-α blocking agents such as infliximab are very effective for treatment of RA, especially for the prevention of articular destruction. We have previously shown that several proteins exhibited extensive changes in their expression after amelioration of RA with infliximab treatment. Among the proteins, connective tissue growth factor(CTGF) has a significantrole for the development of RA. Herein, we review the function of CTGF in the pathogenesis of RA and discuss the possibility of a novel treatment for RA. We propose that CTGF is a potentially novel effector molecule in the pathogenesis of RA. Blocking the CTGF pathways by biological agents may have great beneficial effect in patients with RA. 展开更多
关键词 CONNECTIVE tissue growth facto RHEUMATOID ARTHRITIS OSTEOCLASTS condrocytes Tumor NECROSIS factor-α
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青少年特发性脊柱侧凸患者椎体生长板中Runx2及Ⅹ型胶原表达 被引量:1
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作者 俞扬 王守丰 +3 位作者 邱勇 王斌 朱泽章 朱锋 《中国脊柱脊髓杂志》 CAS CSCD 2008年第9期655-659,I0001,共6页
目的:观察青少年特发性脊柱侧凸(AIS)患者上、下端椎和顶椎椎体生长板凸、凹侧软骨细胞的生物活性差异,探讨其在AIS发生和发展中的作用。方法:在对12例AIS患者行胸椎侧凸前路松解手术或前路矫形手术时获取上、下终椎和顶椎椎体生长板,... 目的:观察青少年特发性脊柱侧凸(AIS)患者上、下端椎和顶椎椎体生长板凸、凹侧软骨细胞的生物活性差异,探讨其在AIS发生和发展中的作用。方法:在对12例AIS患者行胸椎侧凸前路松解手术或前路矫形手术时获取上、下终椎和顶椎椎体生长板,分成凸、凹侧2组,共72枚标本,应用免疫组织化学方法检测Runx2和Ⅹ型胶原蛋白的表达,原位杂交方法检测Runx2 mRNA表达。所有染色结果通过图像分析系统进行半定量分析。结果:AIS患者顶椎椎体生长板凸、凹两侧的Ⅹ型胶原、Runx2和Runx2 mRNA表达总量存在显著性差异(P<0.05)。顶椎椎体生长板凹侧Ⅹ型胶原的表达总量低于下终椎椎体生长板凹侧的表达总量(P<0.05)。顶椎椎体生长板凹侧Runx2的表达总量低于上、下终椎椎体生长板凹侧的表达总量(P<0.05)。顶椎椎体生长板凹侧单一软骨细胞Runx2表达量高于凸侧和上、下终椎椎体生长板凹侧单一软骨细胞的表达(P<0.05)。顶椎椎体生长板凹侧高倍视野下平均Runx2 mRNA表达总量低于上、下终椎椎体生长板的凹侧(P<0.05)。顶椎椎体生长板凸侧单一细胞Runx2 mRNA表达量低于凹侧(P<0.05)。顶椎椎体生长板凹侧高倍视野下平均Ⅹ型胶原阳性细胞密度和Runx2阳性细胞密度低于凸侧和上、下终椎椎体生长板凹侧阳性细胞密度(P<0.05)。结论:AIS患者上、下终椎和顶椎椎体生长板凸、凹侧软骨细胞存在不同的生物活性和细胞动力学,这可能是力学条件改变后的一种继发性改变,但其可能在AIS的进展中发挥重要作用。 展开更多
关键词 特发性脊柱侧凸 椎体 生长板 软骨细胞 RUNX2 X型胶原
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