Role of sphingolipids in murine radiation-induced lung injury: protection by sphingosine 1-phosphate analogs

被引:51
作者
Mathew, Biji
Jacobson, Jeffrey R.
Berdyshev, Evgeny
Huang, Yong [3 ]
Sun, Xiaoguang
Zhao, Yutong
Gerhold, Lynnette M. [4 ]
Siegler, Jessica
Evenoski, Carrie
Wang, Ting
Zhou, Tong
Zaidi, Rafe
Moreno-Vinasco, Liliana
Bittman, Robert [6 ]
Chen, Chin Tu [4 ]
LaRiviere, Patrick J. [4 ]
Sammani, Saad
Lussier, Yves A. [3 ]
Dudek, Steven M.
Natarajan, Viswanathan [2 ]
Weichselbaum, Ralph R. [5 ]
Garcia, Joe G. N. [1 ]
机构
[1] Univ Illinois, Dept Med Pharmacol & Bioengn, Inst Personalized Resp Med, Sect Pulm Crit Care & Sleep Med, Chicago, IL 60612 USA
[2] Univ Illinois, Dept Pharmacol, Chicago, IL 60612 USA
[3] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[4] Univ Chicago, Dept Radiol, Chicago, IL 60637 USA
[5] Univ Chicago, Dept Radiat Oncol, Chicago, IL 60637 USA
[6] CUNY, Queens Coll, Dept Chem & Biochem, Flushing, NY USA
基金
美国国家卫生研究院;
关键词
gene dysregulation; S1P receptors; fTysiponate; FTY720; ENDOTHELIAL-CELLS; ACID SPHINGOMYELINASE; BARRIER ENHANCEMENT; INDUCED APOPTOSIS; GENE-EXPRESSION; VASCULAR LEAK; CERAMIDE; PNEUMONITIS; RECEPTOR; ACTIVATION;
D O I
10.1096/fj.11-183970
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Clinically significant radiation-induced lung injury (RILI) is a common toxicity in patients administered thoracic radiotherapy. Although the molecular etiology is poorly understood, we previously characterized a murine model of RILI in which alterations in lung barrier integrity surfaced as a potentially important pathobiological event and genome-wide lung gene mRNA levels identified dysregulation of sphingolipid metabolic pathway genes. We hypothesized that sphingolipid signaling components serve as modulators and novel therapeutic targets of RILI. Sphingolipid involvement in murine RILI was confirmed by radiation-induced increases in lung expression of sphingosine kinase (SphK) isoforms 1 and 2 and increases in the ratio of ceramide to sphingosine 1-phosphate (S1P) and dihydro-S1P (DHS1P) levels in plasma, bronchoalveolar lavage fluid, and lung tissue. Mice with a targeted deletion of SphK1 (SphK1(-/-)) or with reduced expression of S1P receptors (S1PR1(+/-), S1PR2(-/-), and S1PR3(-/-)) exhibited marked RILI susceptibility. Finally, studies of 3 potent vascular barrier-protective S1P analogs, FTY720, (S)-FTY720-phosphonate (fTyS), and SEW-2871, identified significant RILI attenuation and radiation-induced gene dysregulation by the phosphonate analog, fTyS (0.1 and 1 mg/kg i.p., 2x/wk) and to a lesser degree by SEW-2871 (1 mg/kg i.p., 2x/wk), compared with those in controls. These results support the targeting of S1P signaling as a novel therapeutic strategy in RILI.-Mathew, B., Jacobson, J. R., Berdyshev, E., Huang, Y., Sun, X., Zhao, Y., Gerhold, L. M., Siegler, J., Evenoski, C., Wang, T., Zhou, T., Zaidi, R., Moreno-Vinasco, L., Bittman, R., Chen, C. T., LaRiviere, P. J., Sammani, S., Lussier, Y. A., Dudek, S. M., Natarajan, V., Weichselbaum, R. R., Garcia, J. G. N. Role of sphingolipids in murine radiation-induced lung injury: protection by sphingosine 1-phosphate analogs. FASEB J. 25, 3388-3400 (2011). www. fasebj. org
引用
收藏
页码:3388 / 3400
页数:13
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