Lu Lele, Chai Linlin, Wang Wenping, Yuan Xi, Li Shirong, Cao Chuan
The Third Military Medical University Southwest Plastic Surgery Hospital, Chongqing, 400037, People's Republic of China.
Biol Trace Elem Res. 2017 Apr;176(2):270-277. doi: 10.1007/s12011-016-0827-8. Epub 2016 Aug 27.
Keloids are fibroproliferative disorders characterized by the overabundant deposition of extracellular matrix (ECM), especially collagen and overgrowth of scar tissue in response to cutaneous injury. In this study, we isolated a selenium (Se)-containing polysaccharide (Se-ZGTP-I) from Ziyang green tea and explored its potential therapeutic effects on keloid fibroblasts formation. 3-(4,5-Dimethyl-thiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and annexin V/propidium iodide (PI) staining assays demonstrated that Se-ZGTP-I or neuron-glia 2 (NG2) short hairpin RNA (shRNA) significantly inhibited proliferation of human keloid fibroblasts via induction of apoptosis. Besides, the activation of caspase-3 and the subsequent cleavage of poly (ADP-ribose) polymerase (PARP) were observed in keloid fibroblasts following Se-ZGTP-I (200 and 400 μg/ml) or NG2 shRNA treatment. Moreover, Western blotting analysis showed that treatment of keloid fibroblasts with Se-ZGTP-I (200 and 400 μg/ml) or NG2 shRNA resulted in an increase of pro-apoptotic protein Bax expression and a decrease in expression levels of anti-apoptotic protein Bcl-2 and NG2. In addition, type I collagen biosynthesis and protein expression in keloid fibroblasts following TGF-β1 stimulation were decreased by Se-ZGTP-I (200 and 400 μg/ml) or NG2 shRNA management. Current findings imply that Se-ZGTP-I has a therapeutic potential to intervene and prevent keloid formation and other fibrotic diseases.
瘢痕疙瘩是一种纤维增生性疾病,其特征是细胞外基质(ECM)过度沉积,尤其是胶原蛋白,以及皮肤损伤后瘢痕组织过度生长。在本研究中,我们从紫阳绿茶中分离出一种含硒多糖(Se-ZGTP-I),并探讨了其对瘢痕疙瘩成纤维细胞形成的潜在治疗作用。3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)和膜联蛋白V/碘化丙啶(PI)染色试验表明,Se-ZGTP-I或神经胶质2(NG2)短发夹RNA(shRNA)通过诱导凋亡显著抑制人瘢痕疙瘩成纤维细胞的增殖。此外,在Se-ZGTP-I(200和400μg/ml)或NG2 shRNA处理后的瘢痕疙瘩成纤维细胞中观察到半胱天冬酶-3的激活以及随后聚(ADP-核糖)聚合酶(PARP)的裂解。此外,蛋白质印迹分析表明,用Se-ZGTP-I(200和400μg/ml)或NG2 shRNA处理瘢痕疙瘩成纤维细胞会导致促凋亡蛋白Bax表达增加,抗凋亡蛋白Bcl-2和NG2表达水平降低。此外,Se-ZGTP-I(200和400μg/ml)或NG2 shRNA处理可降低转化生长因子-β1刺激后瘢痕疙瘩成纤维细胞中I型胶原蛋白的生物合成和蛋白表达。目前的研究结果表明,Se-ZGTP-I具有干预和预防瘢痕疙瘩形成及其他纤维化疾病的治疗潜力。