Effects of Thoracic Irradiation on Pulmonary Endothelial Compared to Alveolar Type-II Cells in Fibrosis-Prone C57BL/6NTac Mice

被引:0
作者
Kalash, Ronny [1 ]
Berhane, Hebist [1 ]
Goff, Julie [1 ]
Houghton, Frank [1 ]
Epperly, Michael W. [1 ]
Dixon, Tracy [1 ]
Zhang, Xichen [1 ]
Sprachman, Melissa M. [2 ]
Wipf, Peter [2 ]
Franicola, Darcy [1 ]
Wang, Hong [1 ]
Greenberger, Joel S. [1 ]
机构
[1] Univ Pittsburgh, Dept Radiat Oncol, Inst Canc, Pittsburgh, PA 15232 USA
[2] Univ Pittsburgh, Dept Chem, Ctr Chem Methodol & Lib Dev, Pittsburgh, PA 15260 USA
来源
IN VIVO | 2013年 / 27卷 / 03期
关键词
Ionizing irradiation; endothelial cells; alveolar type-II cells; motility; RADIATION-DAMAGE; GROWTH-FACTOR; IN-VITRO; EXPRESSION; STRATEGIES; ADHESION;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: Thoracic irradiation results in an acute inflammatory response, latent period, and late fibrosis. Little is known about the mechanisms involved in triggering late radiation fibrosis. Materials and Methods: Thoracic irradiated fibrosis prone C57BL/6NTac mice were followed for detectable mRNA transcripts in isolated lung cells and microRNA in whole-tissues, and the effect of administration of water-soluble oxetanyl sulfoxide MMS350 was studied. Marrow stromal cell motility in medium from fibrotic-phase explanted pulmonary endothelial and alveolar type-II cells was measured. Results: RNA and micro-RNA expression in lung correlated with fibrosis. MMS350 reduced pro-fibrotic gene expression in both endothelial and alveolar type-II cells in irradiated mice. Conditioned medium from irradiated cells did not alter cell motility in vitro. Conclusion: These studies should facilitate identification of potential new drug targets for ameliorating irradiation-induced pulmonary fibrosis.
引用
收藏
页码:291 / 297
页数:7
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