中华皮肤科杂志 ›› 2015, Vol. 48 ›› Issue (5): 338-342.

• 论著 • 上一篇    下一篇

连续长波紫外线照射对人皮肤成纤维细胞胞吞、降解弹性蛋白的影响

刘晨1,2,赖维3,许庆芳4,侯巍5,郑跃4,吴琳6,王宇健6   

  1. 1.
    2. 中山大学附属第三医院皮肤性病科
    3. 广州中山大学附属第三医院皮肤科
    4. 中山大学附属第三医院皮肤科
    5. 新疆医科大学第一附属医院
    6. 中山大学附属三院皮肤科
  • 收稿日期:2014-08-21 修回日期:2015-01-09 出版日期:2015-05-15 发布日期:2015-04-30
  • 通讯作者: 赖维 E-mail:drlaiwei@163.com
  • 基金资助:

    国家自然科学基金

Effects of repetitive ultraviolet A radiation on the endocytosis and degradation of elastin by human skin fibroblasts

  • Received:2014-08-21 Revised:2015-01-09 Online:2015-05-15 Published:2015-04-30
  • Contact: Wei Lai E-mail:drlaiwei@163.com

摘要:

目的 研究连续长波紫外线(UVA)照射对人皮肤成纤维细胞胞吞和胞内降解细胞外弹性蛋白能力的影响,探讨光老化皮肤弹性蛋白堆积的机制。 方法 将人皮肤成纤维细胞分为空白对照组和连续UVA照射组,连续UVA照射组予连续7 d每天9.9 J/cm2 UVA照射以构建人皮肤成纤维细胞慢性光损伤模型。用流式细胞仪和衰老相关β半乳糖苷酶染色法分别检测细胞周期和细胞老化程度以验证模型。用荧光示踪技术和共轭淬灭技术,比较两组细胞对培养基中弹性蛋白的胞吞情况和对胞吞进入细胞的弹性蛋白的降解情况差异。 结果 与空白对照组相比,连续UVA照射组G1期细胞比例和衰老细胞比例明显增高,人皮肤成纤维细胞慢性光损伤模型构建成功。空白对照组人皮肤成纤维细胞在与弹性蛋白共孵育24、48、72 h后对弹性蛋白的胞吞率依次为(10.0 ± 1.4)%、(27.8 ± 4.2)%、(39.9 ± 4.1)%,连续UVA照射组人皮肤成纤维细胞在对应时间点的胞吞率依次为(9.9 ± 1.6)%、(28.3 ± 5.1)%、(42.0 ± 5.7)%,在相同时间点两组细胞对弹性蛋白的胞吞率差异均无统计学意义(均P > 0.05)。空白对照组人皮肤成纤维细胞在与弹性蛋白共孵育24、48、72 h后,胞内降解内吞入胞的弹性蛋白的细胞百分率依次为(7.7 ± 0.9)%、(22.8 ± 1.8)%、(33.9 ± 3.1)%,而连续UVA照射组人皮肤成纤维细胞在对应时间点依次为(4.2 ± 1.1)%、(16.5 ± 2.4)%、(26.7 ± 2.6)%,均较对照组显著降低(均P < 0.05)。 结论 连续7 d每日9.9 J/cm2 UVA照射对人皮肤成纤维细胞胞吞弹性蛋白的能力没有明显影响,却使细胞对胞吞的弹性蛋白的胞内降解能力下降。

Abstract:

Liu Chen*, Lai Wei, Xu Qingfang, Hou Wei, Zheng Yue, Wu Lin, Wang Yujian. *Department of Dermatology and Venereology, Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China Corresponding author: Lai Wei, Email: drlaiwei@163.com 【Abstract】 Objective To investigate the effects of repetitive ultraviolet A (UVA) radiation on the endocytosis and intracellular degradation of extracellular elastin by human dermal fibroblasts (HDFs), and to explore the mechanism responsible for elastin accumulation in photoaging skin. Methods Cultured HDFs were divided into two groups: repetitive UVA radiation group treated with UVA radiation (9.9 J/cm2) once a day for seven consecutive days to establish a chronic photodamage model, and blank control group receiving no treatment. For the verification of the model, flow cytometry was performed to detect cell cycle, and senescence-associated β-galactosidase staining to determine the degree of cell senescence. Fluorescent tracer technique and conjugated polymer-based fluorescence quenching technique were conducted to observe the endocytosis and intracellular degradation of extracellular elastin in culture media by HDFs in these groups. Results Compared with the blank control group, the repetitive UVA radiation group showed increased proportions of G1-phase cells and senescent cells, which confirmed the successful establishment of chronic photodamage model in the repetitive UVA radiation group. After coculture with elastin for 24, 48 and 72 hours, the endocytosis rate of elastin was 10.0% ± 1.4%, 27.8% ± 4.2% and 39.9% ± 4.1% respectively in the blank control group, 9.9% ± 1.6%, 28.3% ± 5.1% and 42.0% ± 5.7% respectively in the repetitive UVA radiation group, with no significant difference between the two groups at the three time points (all P > 0.05). The percentage of cells showing intracellular degradation of extracellular elastin was significantly lower in the repetitive UVA radiation group than in the blank control group (4.2% ± 1.1% vs. 7.7% ± 0.9% at 24 hours, 16.5% ± 2.4% vs. 22.8% ± 1.8% at 48 hours, 26.7% ± 2.6% vs. 33.9% ± 3.1% at 72 hours, all P < 0.05). Conclusions UVA radiation at 9.9 J/cm2 for 7 consecutive days can decrease the intracellular degradation of extracellular elastin by HDFs, but has no obvious effect on endocytosis of elastin.

中图分类号: 

  • R758.1