Senescent fibroblasts induce moderate stress in lung epithelial cells in vitro

被引:11
作者
Bartling, B [1 ]
Rehbein, G [1 ]
Silber, RE [1 ]
Simm, A [1 ]
机构
[1] Univ Halle Wittenberg, Dept Cardiothorac Surg, Klin Herz & Thoraxchirurg, D-06120 Halle, Saale, Germany
关键词
fibroblast; aging; lung epithelial cell; proliferation; cell death; reactive oxygen species;
D O I
10.1016/j.exger.2006.02.006
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
Epithelial-mesenchymal interactions contribute to functionality and integrity of the lung epithelium, which might change during ageing and associated cellular ageing. Therefore, we studied the effect of senescent versus pre-senescent lung fibroblasts (WI-38) on mitogenic and stress-protective factors in lung epithelial cells (H358). By use of conditioned medium, we found a growth promoting impact of fibroblasts compared with control medium from epithelial cells associated with activation of ERK1/2, Akt, p70S6K, and EGF receptor. Although senescent fibroblasts mediated similar growth stimulation compared with pre-senescent cells, we observed less protection against spontaneous mitochondrial dysfunction in vitro, higher production of reactive oxygen species and activation of copper/zinc superoxide dismutase. Moreover, senescent cells induced activation of caspase-3/7 in epithelial cells, which was associated with down-regulation of the caspase-inhibitory protein XIAP. In summary, senescent lung fibroblasts induce moderate stress in lung epithelial cells in vitro without affecting growth signaling. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:532 / 539
页数:8
相关论文
共 32 条
[1]
INDUCTION IN VITRO OF TRACHEAL BUDS BY PULMONARY MESENCHYME GRAFTED ON TRACHEAL EPITHELIUM [J].
ALESCIO, T ;
CASSINI, A .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1962, 150 (02) :83-&
[2]
Barcellos-Hoff MH, 2000, CANCER RES, V60, P1254
[3]
Proliferative stimulus of lung fibroblasts on lung cancer cells is impaired by the receptor for advanced glycation end-products [J].
Bartling, B ;
Demling, N ;
Silber, RE ;
Simm, A .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2006, 34 (01) :83-91
[4]
Down-regulation of the receptor for advanced glycation end-products (RAGE) supports non-small cell lung carcinoma [J].
Bartling, B ;
Hofmann, HS ;
Weigle, B ;
Silber, RE ;
Simm, A .
CARCINOGENESIS, 2005, 26 (02) :293-301
[5]
Endogenously released Smac is insufficient to mediate cell death of human lung carcinoma in response to etoposide [J].
Bartling, B ;
Lewensohn, R ;
Zhivotovsky, B .
EXPERIMENTAL CELL RESEARCH, 2004, 298 (01) :83-95
[6]
TNF-α and IL-1α induce apoptosis in subconfluent rat mesangial cells.: Evidence for the involvement of hydrogen peroxide and lipid peroxidation as second messengers [J].
Böhler, T ;
Waiser, J ;
Hepburn, H ;
Gaedeke, J ;
Lehmann, C ;
Hambach, P ;
Budde, K ;
Neumayer, HH .
CYTOKINE, 2000, 12 (07) :986-991
[7]
Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery [J].
Datta, SR ;
Dudek, H ;
Tao, X ;
Masters, S ;
Fu, HA ;
Gotoh, Y ;
Greenberg, ME .
CELL, 1997, 91 (02) :231-241
[8]
Mesenchymal-epithelial interactions in lung development and repair: are modeling and remodeling the same process? [J].
Demayo, F ;
Minoo, P ;
Plopper, CG ;
Schuger, L ;
Shannon, J ;
Torday, JS .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2002, 283 (03) :L510-L517
[9]
IAPs block apoptotic events induced by caspase-8 and cytochrome c by direct inhibition of distinct caspases [J].
Deveraux, QL ;
Roy, N ;
Stennicke, HR ;
Van Arsdale, T ;
Zhou, Q ;
Srinivasula, SM ;
Alnemri, ES ;
Salvesen, GS ;
Reed, JC .
EMBO JOURNAL, 1998, 17 (08) :2215-2223
[10]
Redox control of signal transduction, gene expression and cellular senescence [J].
Esposito, F ;
Ammendola, R ;
Faraonio, R ;
Russo, T ;
Cimino, F .
NEUROCHEMICAL RESEARCH, 2004, 29 (03) :617-628