Alteration of the TGF-β/SMAD pathway in intrinsically and UV-induced skin aging

被引:67
作者
Han, KH
Choi, HR
Won, CH
Chung, JH
Cho, KH
Eun, HC
Kim, KH [1 ]
机构
[1] Seoul Natl Univ Hosp, Clin Res Inst, Dept Dermatol, Lab Cutaneous Aging Res, Seoul 110744, South Korea
[2] Seoul Natl Univ Hosp, Clin Res Inst, Seoul 110744, South Korea
关键词
aging; Photoaging; T beta RII; Smad7; pSmad2;
D O I
10.1016/j.mad.2004.11.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In an effort to characterize transforming growth factor (TGF-beta) signaling and to determine its association with the aging and photoaging processes, we directly compared the expressions of TGF-beta/SMAD in intrinsically aged and photoaged human skin in vivo. By using an RNase protection assay and by immunohistochemistry, we found that the expression levels of T beta RII mRNA and protein in the epidermis of the forearm (sun-exposed) of the elderly were significantly lower than that of the upper-inner arm (sun-protected) skin of the same individual. In the epidermis, the expressions of Smad7 mRNA in both the intrinsically aged and photoaged skin of the elderly were higher than in the sun-protected skin of the young, and this was elevated in the photoaged epidermis. Decreased pSmad2 immunoreactivity was observed in the epidermis of photoaged forearm skin versus matched intrinsically aged skin. This decrease was also found in the epidermis of upper-inner arm skin of the elderly versus the young. These results suggest that the UV-induced down-regulation of T beta RII and the concerted over-expression of Smad7 may trigger the inhibition of the TGF-beta-induced phosphorylation of Smad2. (c) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:560 / 567
页数:8
相关论文
共 22 条
[1]   CHARACTERIZATION OF THE PROMOTER REGION OF THE HUMAN TRANSFORMING GROWTH-FACTOR-BETA TYPE-II RECEPTOR GENE [J].
BAE, HW ;
GEISER, AG ;
KIM, DH ;
CHUNG, MT ;
BURMESTER, JK ;
SPORN, MB ;
ROBERTS, AB ;
KIM, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (49) :29460-29468
[2]   Structure and expression of the promoter for the R4/ALK5 human type I transforming growth factor-beta receptor: Regulation by TGF-beta [J].
Bloom, BB ;
Humphries, DE ;
Kuang, PP ;
Fine, A ;
Goldstein, RH .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1996, 1312 (03) :243-248
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]  
Chung JH, 2001, ARCH DERMATOL, V137, P1043
[5]   c-Jun-dependent inhibition of cutaneous procollagen transcription following ultraviolet irradiation is reversed by all-trans retinoic acid [J].
Fisher, GJ ;
Datta, S ;
Wang, ZQ ;
Li, XY ;
Quan, TH ;
Chung, JH ;
Kang, SW ;
Voorhees, JJ .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (05) :663-670
[6]   Smad-dependent stimulation of type I collagen gene expression in human skin fibroblasts by TGF-β involves functional cooperation with p300/CBP transcriptional coactivators [J].
Ghosh, AK ;
Yuan, W ;
Mori, Y ;
Varga, J .
ONCOGENE, 2000, 19 (31) :3546-3555
[7]   Proliferation and differentiation of the keratinocytes in hyperplastic epidermis overlying dermatofibroma - Immunohistochemical characterization. [J].
Han, KH ;
Huh, CH ;
Cho, KH .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2001, 23 (02) :90-98
[8]   Smads mediate signaling of the TGFβ superfamily in normal keratinocytes but are lost during skin chemical carcinogenesis [J].
He, W ;
Cao, TY ;
Smith, DA ;
Myers, TE ;
Wang, XJ .
ONCOGENE, 2001, 20 (04) :471-483
[9]   TGF-beta signalling from cell membrane to nucleus through SMAD proteins [J].
Heldin, CH ;
Miyazono, K ;
tenDijke, P .
NATURE, 1997, 390 (6659) :465-471
[10]  
JI C, 1997, J BIOL CHEM, P27234