阿魏酸钠对人皮肤增生性瘢痕成纤维细胞增殖和凋亡的调控作用及其信号机制

王畅; 陈炜; 王宝家

doi:10.3760/cma.j.cn501120-20201120-00484

阿魏酸钠对人皮肤增生性瘢痕成纤维细胞增殖和凋亡的调控作用及其信号机制

doi: 10.3760/cma.j.cn501120-20201120-00484

王畅¹,
陈炜²,
王宝家^1,, ,

1.
成都中医药大学基础医学院，成都　　611137
2.
西南交通大学网路教育学院，成都　　610031

基金项目:

四川省教育厅自然科学重点项目 18ZA0184

成都中医药大学科技发展基金 ZRQN1760

详细信息

通讯作者:
王宝家，Email：381697749@qq.com

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出版历程
- 收稿日期: 2020-11-20
- 网络出版日期: 2022-07-20
- 刊出日期: 2022-05-20

Regulatory effects and signaling mechanism of sodium ferulate on the proliferation and apoptosis of human skin hypertrophic scar fibroblasts

1.
School of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China
2.
Internet Connections College of Education, Southwest Jiaotong University, Chengdu 610031, China

Funds:

Key Natural Science Project of Sichuan Provincial Department of Education 18ZA0184

Science and Technology Development Fund of Chengdu University of Traditional Chinese Medicine ZRQN1760

More Information

Corresponding author: Wang Baojia, Email: 381697749@qq.com

摘要

摘要:
目的探讨阿魏酸钠对人皮肤增生性瘢痕成纤维细胞（HSFb）增殖、凋亡的调控作用和信号机制。
方法采用实验研究方法。取第4~6代人皮肤HSFb用于后续实验。将HSFb分别与终质量浓度1、1×10^-1、1×10^-2、1×10^-3、1×10^-4、1×10^-5、1×10^-6 mg/mL阿魏酸钠共培养48 h，采用噻唑蓝法测定细胞吸光度值并采用线性回归法分析阿魏酸钠的半数致死浓度（LC50），样本数为6。将HSFb分别与终质量浓度0.1、0.2、0.3、0.4 mg/mL的阿魏酸钠共培养24、48、72、96 h后，采用噻唑蓝法测定细胞吸光度值并计算细胞增殖抑制率（样本数为3）。取细胞，按随机数字表法分为采用相应终质量浓度阿魏酸钠处理的0.300 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.003 mg/mL阿魏酸钠组和不进行任何处理的阴性对照组。培养72 h后，采用噻唑蓝法测定细胞吸光度值（样本数为5），采用透射电子显微镜观察细胞微观形态（样本数为3），采用原位末端标记（TUNEL）法检测细胞凋亡情况并计算凋亡指数（样本数为4），采用免疫组织化学法检测B淋巴细胞瘤-2（Bcl-2）、Bcl-2相关X蛋白（Bax）、胱天蛋白酶3（caspase-3）蛋白表达（样本数为4），采用蛋白质印迹法检测转化生长因子β₁（TGF-β₁）、磷酸化Smad2/3、磷酸化Smad4、磷酸化Smad7的蛋白表达（样本数为4）。对数据行单因素方差分析、Dunnett检验。
结果阿魏酸钠的LC50为0.307 5 mg/mL。培养24~96 h，4个质量浓度阿魏酸钠处理的细胞增殖抑制率均呈先升高后降低的趋势，于培养72 h达到最高，选择72 h作为后续实验的处理时间。培养72 h后，0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组细胞吸光度值分别为0.57±0.06、0.53±0.04、0.45±0.05，均明显低于阴性对照组的0.69±0.06（P<0. 01）。培养72 h后，与阴性对照组比较，用阿魏酸钠处理的3组细胞出现不同程度的核固缩或断裂、裂解，染色质丢失，胞质中可见线粒体肿胀、粗面内质网扩张，局部逐渐空泡化。培养72 h后，与阴性对照组比较，0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组细胞凋亡指数均显著升高（P<0. 05或P<0. 01）。培养72 h后，与阴性对照组比较，0.300 mg/mL阿魏酸钠组细胞Bcl-2蛋白表达量明显减少（P<0. 01），0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组细胞Bax蛋白表达量均明显增加（P<0. 05），0.300 mg/mL阿魏酸钠组细胞caspase-3蛋白表达量显著增加（P<0.01）。培养72 h后，与阴性对照组比较，0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组细胞TGF-β₁、磷酸化Smad2/3、磷酸化Smad4蛋白表达量均明显减少（P<0. 05或P<0. 01），0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组细胞磷酸化Smad7蛋白表达量均显著增加（P<0.01）。
结论阿魏酸钠可通过阻断TGF-β/Smad信号通路上的关键蛋白的表达，协同激活线粒体凋亡途径共同发挥抑制人皮肤HSFb增殖和促进人皮肤HSFb凋亡的作用。
- 瘢痕 /
- 成纤维细胞 /
- 细胞增殖 /
- 细胞凋亡 /
- 阿魏酸钠 /
- 转化生长因子β/Smad信号通路
Abstract:
Objective To investigate the regulatory effects and signaling mechanism of sodium ferulate on the proliferation and apoptosis of human skin hypertrophic scar fibroblasts (HSFbs).
Methods The experimental research methods were used. The 4^th-6^th passage of HSFbs from human skin were used for the following experiments. HSFbs were co-cultured with sodium ferulate at final mass concentrations of 1, 1×10^-1, 1×10^-2, 1×10^-3, 1×10^-4, 1×10^-5, and 1×10^-6 mg/mL for 48 hours, and methyl thiazolyl tetrazolium method was used to determine the cell absorbance values and linear regression was used to analyze the half lethal concentration (LC50) of sodium ferulate (n=6). HSFbs were co-cultured with sodium ferulate at final mass concentrations of 0.1, 0.2, 0.3, and 0.4 mg/mL for 24, 48, 72, and 96 hours, and methyl thiazolyl tetrazolium method was used to determine the cell absorbance values and the cell proliferation inhibition rate was calculated (n=3). According to the random number table, the cells were divided into 0.300 mg/mL sodium ferulate group, 0.030 mg/mL sodium ferulate group, 0.003 mg/mL sodium ferulate group treated with sodium ferulate at corresponding final mass concentrations, and negative control group without any treatment. After 72 hours of culture, the cell absorbance values were determined by methyl thiazolyl tetrazolium method (n=5), the microscopic morphology of cells was observed by transmission electron microscope (n=3), the cell apoptosis was detected by TdT-mediated dUTP-biotin nick end labeling (TUNEL) assay and the apoptosis index was calculated (n=4), the protein expressions of B lymphocystoma-2 (Bcl-2), Bcl-2-associated X protein (Bax), and cysteine aspartic acid specific protease-3 (caspase-3) were determined by immunohistochemistry (n=4), and the protein expressions of transformed growth factor β₁ (TGF-β₁), phosphorylated Smad2/3, phosphorylated Smad4, and phosphorylated Smad7 were detected by Western blotting (n=4). Data were statistically analyzed with one-way analysis of variance and Dunnett test.
Results The LC50 of sodium ferulate was 0.307 5 mg/mL. After being cultured for 24-96 hours, the cell proliferation inhibition rates of cells treated with sodium ferulate at four different mass concentrations tended to increase at first but decrease later, which reached the highest after 72 hours of culture, so 72 hours was chosen as the processing time for the subsequent experiments. After 72 hours of culture, the cell absorbance values in 0.003 mg/mL sodium ferulate group, 0.030 mg/mL sodium ferulate group, and 0.300 mg/mL sodium ferulate group were 0.57±0.06, 0.53±0.04, 0.45±0.05, respectively, which were significantly lower than 0.69±0.06 in negative control group (P<0.01). After 72 hours of culture, compared with those in negative control group, the cells in the three groups treated with sodium ferulate showed varying degrees of nuclear pyknosis, fracture, or lysis, and chromatin loss. In the cytoplasm, mitochondria were swollen, the rough endoplasmic reticulum was expanded, and local vacuolation gradually appeared. After 72 hours of culture, compared with that in negative control group, the apoptosis indexes of cells were increased significantly in 0.003 mg/mL sodium ferulate group, 0.030 mg/mL sodium ferulate group, and 0.300 mg/mL sodium ferulate group (P<0.05 or P<0.01). After 72 hours of culture, compared with those in negative control group, the protein expressions of Bcl-2 of cells in 0.300 mg/mL sodium ferulate group was significantly decreased (P<0.01), the protein expressions of Bax of cells in 0.030 mg/mL sodium ferulate group and 0.300 mg/mL sodium ferulate group were significantly increased (P<0.05), and the protein expression of caspase-3 of cells in 0.300 mg/mL sodium ferulate group was significantly increased (P<0.01). After 72 hours of culture, compared with those in negative control group, the protein expression levels of TGF-β₁, phosphorylated Smad2/3, and phosphorylated Smad4 of cells in 0.030 mg/mL sodium ferulate group and 0.300 mg/mL sodium ferulate group were significantly decreased (P<0.05 or P<0.01), and the protein expression levels of phosphorylated Smad7 of cells in 0.003 mg/mL sodium ferulate group, 0.030 mg/mL sodium ferulate group, and 0.300 mg/mL sodium ferulate group were significantly increased (P<0.01).
Conclusions Sodium ferulate can inhibit the proliferation of HSFbs of human skin and promote the apoptosis of HSFbs of human skin by blocking the expression of key proteins on the TGF-β/Smad signaling pathway and synergistically activating the mitochon- drial apoptosis pathway.
- Cicatrix /
- Fibroblasts /
- Cell proliferation /
- Apoptosis /
- Sodium ferulate /
- Transforming growth factor β/Smad signaling pathway
王畅：实验操作、采集数据、论文撰写及修改、经费支持；陈炜：实验操作、采集数据；王宝家：统计学分析、论文撰写及修改、经费支持

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1 4个质量浓度阿魏酸钠处理人皮肤增生性瘢痕成纤维细胞96 h内增殖抑制率比较（样本数为3， $\bar{x} \pm s$ ）

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2 4组人皮肤增生性瘢痕成纤维细胞培养72 h后吸光度值比较（样本数为5， $\bar{x} \pm s$ ）

注：横坐标下1、2、3、4分别指阴性对照组、0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组；与阴性对照组比较，^aP<0.01

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3 4组人皮肤增生性瘢痕成纤维细胞培养72 h后微观形态的变化透射电子显微镜×20 000，图中标尺为1 μm。3A.阴性对照组细胞核较大，核膜清晰完整，染色质分布较均匀，线粒体、粗面内质网等细胞器结构完整清晰；3B.0.003 mg/mL阿魏酸钠组细胞核染色质凝聚，出现线粒体轻微肿胀、粗面内质网扩展；3C.0.030 mg/mL阿魏酸钠组细胞核染色质凝聚，粗面内质网出现扩张并呈囊泡状；3D.0.300 mg/mL阿魏酸钠组细胞核染色质溶解、胞质凝聚，粗面内质网扩张、线粒体肿胀较图3B、3C更为明显，局部出现空泡化

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4 4组人皮肤增生性瘢痕成纤维细胞培养72 h后凋亡情况二氨基联苯胺-苏木精×200，图中标尺为100 μm。4A、4B、4C、4D.分别为阴性对照组、0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组细胞凋亡情况，图4B、4C、4D凋亡细胞数均较图4A明显增加

注：凋亡细胞核染色为不均匀浅黄色或棕黄色

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5 4组人皮肤增生性瘢痕成纤维细胞培养72 h后凋亡指数比较（样本数为4， $\bar{x} \pm s$ ）

注：横坐标下1、2、3、4分别指阴性对照组、0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组；与阴性对照组比较，^aP<0.05，^bP<0.01

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6 4组人皮肤增生性瘢痕成纤维细胞培养72 h后凋亡相关蛋白表达二氨基联苯胺-苏木精×200，图中标尺为100 μm。6A、6B、6C、6D.分别为阴性对照组、0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组Bcl-2蛋白表达，图6B、6C中Bcl-2蛋白表达均与图6A相近，图6D中Bcl-2蛋白表达较图6A明显减少；6E、6F、6G、6H.分别为阴性对照组、0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组Bax蛋白表达，图6F中Bax蛋白表达与图6E相近，图6G、6H中Bax蛋白表达均较图6E明显增加；6I、6J、6K、6L.分别为阴性对照组、0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组caspase-3蛋白表达，图6J、6K中caspase-3蛋白表达均与图6I相近，图6L中caspase-3蛋白表达较图6I明显增加

注：细胞核染色为棕色或棕黄色示B淋巴细胞瘤-2（Bcl-2）阳性表达，细胞质染色为棕色或棕黄色示Bcl-2相关X蛋白（Bax）、胱天蛋白酶3 （caspase-3）阳性表达

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7 蛋白质印迹法检测 4组人皮肤增生性瘢痕成纤维细胞培养72 h后TGF-β/Smad信号通路蛋白表达

注：TGF-β₁为转化生长因子β₁；条带上方的 1、2、3、4分别指阴性对照组、0.003 mg/mL阿魏酸钠组、0.030 mg/mL阿魏酸钠组、0.300 mg/mL阿魏酸钠组

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表1 4组人皮肤增生性瘢痕成纤维细胞培养72 h后凋亡相关蛋白表达量比较（ $\bar{x} \pm s$ ）

组别	样本数	Bcl-2	Bax	caspase-3
阴性对照组	4	0.157 1±0.002 3	0.214±0.010	0.152 8±0.002 7
0.003 mg/mL阿魏酸钠组	4	0.154 2±0.002 8	0.214±0.007	0.155 1±0.002 3
0.030 mg/mL阿魏酸钠组	4	0.154 8±0.002 7	0.230±0.006^b	0.159 2±0.005 8
0.300 mg/mL阿魏酸钠组	4	0.149 9±0.002 6^a	0.237±0.012^b	0.163 8±0.001 2^a
F值		5.28	6.80	7.81
P值		0.015	0.006	0.004
注：Bcl-2为B淋巴细胞瘤-2，Bax为 Bcl-2相关X蛋白，caspase-3为胱天蛋白酶3；与阴性对照组比较，^aP<0.01，^bP<0.05

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表2 4组人皮肤增生性瘢痕成纤维细胞培养72 h后TGF-β/Smad信号通路蛋白表达比较（ $\bar{x} \pm s$ ）

组别	样本数	TGF-β₁	磷酸化Smad2/3	磷酸化Smad4	磷酸化Smad7
阴性对照组	4	1.00	1.00	1.00	1.00
0.003 mg/mL阿魏酸钠组	4	0.93±0.07	0.97±0.03	0.98±0.06	1.24±0.06^b
0.030 mg/mL阿魏酸钠组	4	0.84±0.07^a	0.89±0.03^b	0.86±0.10^a	1.22±0.03^b
0.300 mg/mL阿魏酸钠组	4	0.82±0.06^b	0.85±0.07^b	0.81±0.07^a	1.17±0.04^b
F值		8.36	10.79	7.74	34.89
P值		0.003	0.001	0.004	<0.001
注：TGF-β₁为转化生长因子β₁；与阴性对照组比较，^aP<0.05，^bP<0.01

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