Gelinas Richard, Chesler Elissa J, Vasconcelos Daphne, Miller Darla R, Yuan Yue, Wang Kai, Galas David
Battelle Memorial Institute, Columbus, OH; ; Institute for Systems Biology, Seattle, WA, USA.
Pharmgenomics Pers Med. 2011;4:35-45. doi: 10.2147/PGPM.S22475. Epub 2011 Jul 4.
The antineoplastic drug bleomycin leads to the side effect of pulmonary fibrosis in both humans and mice. We challenged genetically diverse inbred lines of mice from the Collaborative Cross with bleomycin to determine the heritability of this phenotype. Sibling pairs of mice from 40 lines were treated with bleomycin. Lung disease was assessed by scoring lung pathology and by measuring soluble collagen levels in lavage fluid. Serum micro ribonucleic acids (miRNAs) were also measured. Inbred sibling pairs of animals demonstrated high coinheritance of the phenotypes of disease susceptibility or disease resistance. The plasma levels of one miRNA were clearly correlated in sibling mice. The results showed that, as in humans, the lines that comprise the Collaborative Cross exhibited wide genetic variation in response to this drug. This finding suggests that the genetically diverse Collaborative Cross animals may reveal drug effects that might be missed if a study were based on a conventional mouse strain.
抗肿瘤药物博来霉素会在人类和小鼠中引发肺纤维化的副作用。我们用博来霉素对来自协作杂交的基因多样化近交系小鼠进行挑战,以确定该表型的遗传性。来自40个品系的小鼠同胞对接受了博来霉素治疗。通过对肺部病理进行评分以及测量灌洗液中的可溶性胶原蛋白水平来评估肺部疾病。还检测了血清微小核糖核酸(miRNA)。近交动物同胞对表现出疾病易感性或抗病性表型的高度共遗传性。一种miRNA的血浆水平在同胞小鼠中明显相关。结果表明,与人类一样,构成协作杂交的品系对这种药物的反应表现出广泛的遗传变异。这一发现表明,基因多样化的协作杂交动物可能会揭示出如果研究基于传统小鼠品系可能会遗漏的药物效应。