Lu Changhuai, Liu Zhijun, Zhang Hongbo, Duan Yang, Cao Yanlin
Department of Spine Disease Area of Orthopedics and Traumatology, No.1 Traditional Chinese Medicine Hospital of Changde, Changde Hospital Affiliated to Hunan University of Traditional Chinese Medicine, Changde Hunan, 415000, P.R.China.
Department of Spinal Surgery, Zhujiang Hospital of Southern Medical University, Guangzhou Guangdong, 510282,
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2019 Jun 15;33(6):730-735. doi: 10.7507/1002-1892.201811140.
To investigate the mechanism of p38 mitogen activated protein kinase (MAPK) signaling pathway in regulating the hyperplasia and hypertrophy of human lumbar ligamentum flavum via transforming growth factor β (TGF-β )/connective tissue growth factor (CTGF).
The lumbar ligamentum flavum tissue taken from patient with lumbar intervertebral disc herniation was isolated by collagenase-predigested explant cultures. The ligamentum flavum cells were treated with the extracellular regulated protein kinase pathway blocker PD98059, c-Jun N-terminal kinase pathway blocker SP600125, and p38 pathway blocker SB203580, and then the mRNA expressions of CTGF, collagen type Ⅰ, and collagen type Ⅲ were detected by real-time fluorescence quantitative PCR (qRT-PCR). The ligamentum flavum cells were divided into 4 groups, and transfected with small interfering RNA (siRNA), p38 siRNA, siRNA+3 ng/mL TGF-β , and p38 siRNA+3 ng/mL TGF-β in groups A, B, C, and D, respectively. After 24 hours of transfection, immunofluorescence staining was performed to observe the expressions of p38 and phosphorylation p38 (p-p38); the relative mRNA expressions of CTGF, collagen type Ⅰ, and collagen type Ⅲ in each group were detected by qRT-PCR; the protein expression of CTGF in each group was detected by Western blot.
p38 pathway blocker SB203580 could significantly reduce the relative mRNA expressions of CTGF, collagen type Ⅰ, and collagen type Ⅲ ( <0.05). After 24 hours of transfection, immunofluorescence staining showed positive staining with p38 and p-p38 expressions in groups A, C, and D and negative staining in group B. Compared with group A, the relative mRNA expressions of CTGF, collagen type Ⅰ, and collagen type Ⅲ and relative protein expression of CTGF in group B decreased significantly ( <0.05), while those in groups C and D increased significantly ( <0.05); and those indicators significantly increased in group C than in group D ( <0.05).
TGF-β /CTGF based on the p38 MAPK signaling pathway play an important role in the occurance and development of hypertrophy of human lumbar ligamentum flavum.
探讨p38丝裂原活化蛋白激酶(MAPK)信号通路通过转化生长因子β(TGF-β)/结缔组织生长因子(CTGF)调节人腰椎黄韧带增生和肥大的机制。
采用胶原酶预消化组织块培养法分离取自腰椎间盘突出症患者的腰椎黄韧带组织。用细胞外调节蛋白激酶通路阻滞剂PD98059、c-Jun氨基末端激酶通路阻滞剂SP600125和p38通路阻滞剂SB203580处理黄韧带细胞,然后通过实时荧光定量PCR(qRT-PCR)检测CTGF、Ⅰ型胶原和Ⅲ型胶原的mRNA表达。将黄韧带细胞分为4组,分别在A、B、C、D组中转染小干扰RNA(siRNA)、p38 siRNA、siRNA + 3 ng/mL TGF-β和p38 siRNA + 3 ng/mL TGF-β。转染24小时后,进行免疫荧光染色观察p38和磷酸化p38(p-p38)的表达;通过qRT-PCR检测各组CTGF、Ⅰ型胶原和Ⅲ型胶原的相对mRNA表达;通过蛋白质印迹法检测各组CTGF的蛋白表达。
p38通路阻滞剂SB203580可显著降低CTGF、Ⅰ型胶原和Ⅲ型胶原的相对mRNA表达(P<0.05)。转染24小时后,免疫荧光染色显示A、C、D组p38和p-p38表达呈阳性染色,B组呈阴性染色。与A组相比,B组CTGF、Ⅰ型胶原和Ⅲ型胶原的相对mRNA表达及CTGF的相对蛋白表达显著降低(P<0.05),而C组和D组显著升高(P<0.05);且C组这些指标显著高于D组(P<0.05)。
基于p38 MAPK信号通路的TGF-β/CTGF在人腰椎黄韧带肥大的发生和发展中起重要作用。