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罗格列酮调控光老化成纤维细胞周期阻滞的研究 被引量:1

Regulation of rosiglitazone in the cell cycle arrest of photoaging fibroblasts
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摘要 目的 探讨罗格列酮对光老化成纤维细胞的周期及相关蛋白的影响.方法 采用cck-8法检测罗格列酮对成纤维细胞增殖的影响.罗格列酮预处理成纤维细胞48 h,采用UVB 120 mJ/cm2反复照射4次,照射间隔时间12h,诱导产生细胞光老化模型,继续培养48 h,流式细胞技术检测成纤维细胞周期,Western Blot检测周期相关蛋白p53和p21.结果 低剂量罗格列酮对成纤维细胞的活性无影响.40 μM罗格列酮预处理的光老化成纤维细胞与单纯UVB照射组相比,S期的比例下降了15.9%.与对照组相比,40μM罗格列酮预处理组中成纤维细胞周期相关蛋白p53和p21的表达分别下降了35.7%和27.7%.结论 罗格列酮可降低光老化成纤维细胞周期的相关蛋白p53和p21的表达,缓解UVB引起的光老化成纤维细胞的S期阻滞,可能对光老化成纤维细胞具有某种保护作用. Objective To investigate the influence of rosiglitazone in cell cycle and associated proteins. Methods The influence of rosiglitazone on fibroblasts proliferation was measured by cck-8 assay. After rosiglitazone pretreatment for 48 h, fibroblasts were irradiated by a series of 4 UVB exposures at the dose of 120 mJ/cm2 with an interval time of 12 h. The influence of rosiglitazone on fibroblasts cycle was analyzed by flow cytometry and the expressions of cell cycle regulatory proteins p53 and p21 were evaluated by Western Blot 48 h after the last exposure. Results No modification in the proliferative activity of MDFs was observed at any dose tested up to 80 μM after 48 h ( P 〈0.01 ). The cell cycle arrest in S phase of fibroblasts pretreated with rosiglitazone was 15.9 % less than the UVB group. The expressions of cell cycle regulatory proteins p53 and p21 were decreased by 35.7% and 27.7% respectively compared with UVB group. Conclusion Rosislitazone could decreased the expressions of p53 and p21, cell cycle regulatory proteins of photoaging fibroblasts, relieve the cell cycle arrest of photoaging fibroblasts caused by UVB, so its application may have some protective effect on photoaging fibroblasts.
出处 《中国美容整形外科杂志》 CAS 2015年第7期436-440,共5页 Chinese Journal of Aesthetic and Plastic Surgery
基金 国家自然科学基金资助项目(81272125 81301642) 上海市卫生系统优秀学科带头人培养计划资助项目(XBP,2011033) 863项目资助项目(SS2014AA020705)
关键词 罗格列酮 过氧化物酶体增殖物激活受体Γ 光老化 成纤维细胞 细胞周期 Rosiglitazone Peroxisome proliferator-activated receptor Photoaging Fibroblasts Cellcycle
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  • 1Kohl E, Steinbauer J, Landthaler M, et al. Skin ageing[ J]. J Eur Acad Dermatol Venereol, 2011,25 (8) :873-884.
  • 2Fisher GJ, Varani J, Voorhees JJ. Looking older: fibroblast col- lapse and therapeutic implications [ J ]. Arch Dermatol, 2008, 144(5 ) :666-672.
  • 3刘天一,曾继平.脂肪来源干细胞在创面愈合和衰老皮肤中的应用[J].中国美容整形外科杂志,2012,23(6):321-324. 被引量:5
  • 4Zeng JP, Bi B, Chen L, et al. Repeated exposure of mouse der- mal fibroblasts at a sub-cytotoxic dose of UVB leads to premature senescence: a robust model of cellular photoaging[J]. J Dermatol Sci, 2014,73 ( 1 ) :49-56.
  • 5Lee YH, Lee NH, Bhattarai G, et al. PPARgamma inhibits in- flammatory reaction in oxidative stress induced human diploid fibloblast [ J ]. Cell Biochem Funct, 2010,28 (6) :490-496.
  • 6Chung JH, Seo AY, Chung SW, et al. Molecular mechanism of PPAR in the regulation of age-related inflammation [ J ]. Ageing Res Rev, 2008,7(2) :126-136.
  • 7Gilehrest BA. Photoaging[J]. J Invest Dermatol, 2013,133 (E1) : 2-6.
  • 8Varani J. Fibroblast aging: intrinsic and extrinsic factors [ J ]. Drug Discovery Today : Therapeutic Strategies, 2010,7 (3-4) :65-70.
  • 9杨清建,刘天一,毕波.光老化过程中皮肤成纤维细胞的生物学改变[J].中国美容整形外科杂志,2014,25(8):480-483. 被引量:11
  • 10Ichihashi M, Ueda M, Budiyanto A, et al. UV-induced skin dama ge[J]. Toxicology, 2003,189(1-2) :21-39.

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