Division of Rheumatology, Faculty of Health Sciences, Chris Hani Baragwanath Academic Hospital, P.O. Bertsham 2013, South Africa.
Rheumatology (Oxford). 2012 Jun;51(6):1049-52. doi: 10.1093/rheumatology/ker367. Epub 2012 Jan 27.
To investigate the differential expression of MMP-1, tissue inhibitor of metalloproteinase-1 (TIMP-1) and hepatocyte growth factor (HGF) in clinically involved (affected) and uninvolved (unaffected) skin in patients with SSc.
Punch biopsies from affected forearm and unaffected upper back skin of 16 black South Africans with dcSSc and skin samples of 15 ethnically matched healthy controls were studied. Quantitative mRNA expression of MMP-1, TIMP-1 and HGF was performed by relative reverse transcription quantitative PCR.
Compared with controls, TIMP-1 expression was significantly upregulated in patients, a 796- and 397-fold difference for affected and unaffected skin (P < 0.00001 for both), respectively. Conversely, MMP-1 expression was significantly decreased in patients, a 10- and 12.5-fold difference for affected and unaffected skin (P = 0.0004 for both), respectively. HGF expression was up-regulated in both affected and unaffected skin, a 14- and 18-fold difference (P = 0.004 and P = 0.002), respectively. Within the patient group, HGF expression in affected skin of patients correlated significantly with the European scleroderma disease activity score (r = 0.60, P = 0.013).
Perturbations in gene expression of TIMP-1, MMP-1 and HGF were evident in both affected and unaffected skin of the dcSSc patients. Targeting TIMP-1, which showed the greatest dysregulation, needs to be explored as a way of reducing collagen deposition and fibrosis in dcSSc.
研究 MMP-1、基质金属蛋白酶抑制剂-1(TIMP-1)和肝细胞生长因子(HGF)在系统性硬皮病(SSc)患者的临床受累(病变)和未受累(未病变)皮肤中的差异表达。
对 16 名患有 dcSSc 的南非黑人患者的前臂病变皮肤和上背部未病变皮肤以及 15 名种族匹配的健康对照者的皮肤进行了活检。采用相对逆转录定量 PCR 检测 MMP-1、TIMP-1 和 HGF 的定量 mRNA 表达。
与对照组相比,TIMP-1 在患者中表达明显上调,病变和未病变皮肤分别相差 796 倍和 397 倍(均 P<0.00001)。相反,MMP-1 的表达在患者中明显下调,病变和未病变皮肤分别相差 10 倍和 12.5 倍(均 P=0.0004)。HGF 在病变和未病变皮肤中均上调,分别相差 14 倍和 18 倍(均 P=0.004 和 P=0.002)。在患者组中,HGF 在病变皮肤中的表达与欧洲硬皮病疾病活动评分显著相关(r=0.60,P=0.013)。
dcSSc 患者的病变和未病变皮肤中 TIMP-1、MMP-1 和 HGF 的基因表达均存在明显紊乱。针对 TIMP-1 的靶向治疗,因其表现出最大的失调,需要进一步探索,作为减少 dcSSc 胶原沉积和纤维化的一种方法。