Aryl Hydrocarbon Receptor in Human Dermal Fibroblasts in the Aging Process

被引:1
作者
Gunin, A. G. [1 ]
Kornilova, N. K. [1 ]
机构
[1] Chuvash State Univ, Cheboksary 428015, Russia
基金
俄罗斯基础研究基金会;
关键词
skin; aging; fibroblasts; aryl hydrocarbon receptor; PCNA; AGE-RELATED-CHANGES; SKIN; CELLS; AHR;
D O I
10.1134/S2079057021020053
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The goal of this work was to examine the content of aryl hydrocarbon receptor in human dermal fibroblasts from development until deep aging (from 20 weeks of pregnancy to the age of 85 years) and to determine its role in age-dependent changes in the number of dermal fibroblasts. Aryl hydrocarbon receptor and proliferating cell nuclear antigen (PCNA) were detected with an indirect immunohistochemical technique. The results showed that the portion of fibroblasts with positive staining for aryl hydrocarbon receptor in the dermis gradually increases from 20 weeks of pregnancy to the age of 85 years. The total number and the percentage of PCNA positive fibroblasts in the dermis decreased with the progression of age. The most significant age-dependent reduction in the total and PCNA-positive number of dermal fibroblasts was observed from the antenatal period to the age of 40 years. Correlation analysis showed that both the age-dependent decrease in the number of fibroblasts and the retardation of their proliferation are significantly associated with the age-related increase in the number of dermal fibroblasts positive for aryl hydrocarbon receptor. The results indicate that aryl hydrocarbon receptor is involved in the age-dependent decrease in the number and proliferation of human dermal fibroblasts.
引用
收藏
页码:139 / 144
页数:6
相关论文
共 23 条
[1]   ITE, an endogenous aryl hydrocarbon receptor ligand, suppresses endometrial cancer cell proliferation and migration [J].
Bian Yiding ;
Li Yiran ;
Shrestha, Garima ;
Wen Xiaoli ;
Cai Bailian ;
Wang Kai ;
Wan Xiaoping .
TOXICOLOGY, 2019, 421 :1-8
[2]   Mechanisms of aging and development-A new understanding of environmental damage to the skin and prevention with topical antioxidants [J].
Burke, Karen E. .
MECHANISMS OF AGEING AND DEVELOPMENT, 2018, 172 :123-130
[3]   Expanding Our Understanding of Human Skin Aging [J].
Chang, Anne Lynn S. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2016, 136 (05) :897-899
[4]   Aryl Hydrocarbon Receptor Activation: From Coal to Dioxin [J].
Cline, Abigail ;
Feldman, Steven R. .
JOURNAL OF DERMATOLOGICAL TREATMENT, 2018, 29 (03) :215-216
[5]   Extracellular matrix regulation of fibroblast function: redefining our perspective on skin aging [J].
Cole, Megan A. ;
Quan, Taihao ;
Voorhees, John J. ;
Fisher, Gary J. .
JOURNAL OF CELL COMMUNICATION AND SIGNALING, 2018, 12 (01) :35-43
[6]   Autoimmune disease: Aryl hydrocarbon receptor suppresses inflammation [J].
Crunkhorn S. .
Nature Reviews Drug Discovery, 2018, 17 (7) :470-470
[7]   Aryl hydrocarbon receptor (AHR) is a potential tumour suppressor in pituitary adenomas [J].
Formosa, R. ;
Borg, J. ;
Vassallo, J. .
ENDOCRINE-RELATED CANCER, 2017, 24 (08) :445-457
[8]   Age-related changes in angiogenesis in human dermis [J].
Gunin, Andrei G. ;
Petrov, Vadim V. ;
Golubtzova, Natalia N. ;
Vasilieva, Olga V. ;
Kornilova, Natalia K. .
EXPERIMENTAL GERONTOLOGY, 2014, 55 :143-151
[9]   Age-Related Changes in Proliferation, the Numbers of Mast Cells, Eosinophils, and cd45-Positive Cells in Human Dermis [J].
Gunin, Andrei G. ;
Kornilova, Natalia K. ;
Vasilieva, Olga V. ;
Petrov, Vadim V. .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2011, 66 (04) :385-392
[10]   Aryl hydrocarbon receptor promotes hepatocellular carcinoma tumorigenesis by targeting intestine-specific homeobox expression [J].
Hsu, Shih-Hsien ;
Wang, Li-Ting ;
Chai, Chee-Yin ;
Wu, Chi-Cheng ;
Hsi, Edward ;
Chiou, Shyh-Shin ;
Wang, Shen-Nien .
MOLECULAR CARCINOGENESIS, 2017, 56 (10) :2167-2177