Research on the role and mechanism of indian hedgehog protein in abnormal calcification degeneration of chondrocytes

Xin Zhou, Shaowei Wang, Yan-Fei Yang, Wenjie Niu, Haoran Liang, Jiangong Lu, Kang Wang, L. Pengcui, Xiaochun Wei
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Abstract

Objective To explore the role and mechanism of indian hedgehog (Ihh) in degenerative and abnormal calcification of chondrocyte. Methods Costal chondrocytes were extracted from C57 mice 6 days after birth, By HE staining, Saffron o solid green staining, collagen type Ⅱ immunohistochemical to identify the chondrocyte phenotype The experiment was divided into the ihh high expression group, and Ihh recombinant protein 5 mg/L was added. Ihh knockout group was added to cyclopamine 20 μmol/L. In the blank control group, phosphate buffer solution (PBS) was added. Using real-time quantitative polymerase chain reaction (Real-time PCR) to detect typeⅡcollagen (COLⅡ), type X collagen (COLX), Runt related transcription factor (Runx2), osteocalcin (OCN), alkaline phosphatase (ALP), aggrecan (AGG), progressive ankylosis (ANKH), extracellular nucleotide phosphatase 1 (ENPP1) factors mRNA expression level. Flow cytometry was used to detect the effect of inhibition of Ihh signaling pathway on chondrocyte apoptosis. Results Compared with the control group, the expression of ALP (3.450±1.357 vs. 1.223±0.740), OCN (2.410±0.395 vs. 1.093±0.453), Runx2 (3.057±1.477 vs. 1.144±0.574) and COLX (3.804±1.400 vs. 1.116±0.511) was increased in the high expression group, and the expression of ANKH (0.255±0.042 vs. 1.101±0.471), AGG (0.574±0.355 vs. 1.007±0.126) and COLII (0.670±0.065 vs. 1.027±0.236), ENPP1 (0.354±0.058 vs. 1.091±0.446) was decreased (P<0.05). When the cyclopamine is added, the opposite result appears(P<0.05). Flow cytometry results showed that Inhibition of Ihh signaling pathway can induce apoptosis (t=9.412, P<0.05). Conclusion Ihh can raise COLX, Runx2, OCN and ALP, inhibit the ANKH, ENPP1, AGG and COLⅡ gene expression, and further promote the cartilage cells anomaly calcified. Key words: Indian hedgehog; Chondrocytes; Calcification
印度刺猬蛋白在软骨细胞异常钙化变性中的作用及机制研究
目的探讨印度刺猬在软骨细胞退行性异常钙化中的作用及其机制。方法从C57小鼠出生后6天提取肋软骨细胞,用HE染色、藏红花固绿染色、Ⅱ型胶原免疫组织化学方法鉴定软骨细胞表型。实验分为ihh高表达组,加入5 mg/L的ihh重组蛋白。环胺浓度为20μ。在空白对照组中,加入磷酸盐缓冲溶液(PBS)。采用实时定量聚合酶链反应(real-time PCR)检测Ⅱ型胶原(COLⅡ)、X型胶原(COLX)、Runt相关转录因子(Runx2)、骨钙素(OCN)、碱性磷酸酶(ALP)、聚集蛋白聚糖(AGG)、进行性强直(ANKH)、细胞外核苷酸磷酸酶1(ENPP1)因子mRNA表达水平。流式细胞仪检测抑制Ihh信号通路对软骨细胞凋亡的影响。结果与对照组相比,高表达组ALP(3.450±1.357 vs.1.223±0.740)、OCN(2.410±0.395 vs.1.093±0.453)、Runx2(3.057±1.477 vs.1.144±0.574)和COLX(3.804±1.400 vs.1.116±0.511)表达增加,ANKH(0.255±0.042 vs.1.101±0.471)、AGG(0.574±0.355 vs.1.007±0.126)和COLII(0.670±0.065 vs.1.027±0.236)表达增加,ENPP1(0.354±0.058 vs.1.091±0.446)降低(P<0.05)。当加入环胺时,出现相反的结果(P<0.05),流式细胞仪结果显示抑制Ihh信号通路可诱导细胞凋亡(t=9.412,P<0.05)。结论Ihh可升高COLX、Runx2、OCN和ALP,抑制ANKH、ENPP1、AGG和COLⅡ基因的表达,进一步促进软骨细胞异常钙化。关键词:印度刺猬;软骨细胞;钙化
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