Reynolds Oklahoma Center on Aging, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Department of Physiology, University of Oklahoma Health Sciences Center, 975 NE 10th Street, Oklahoma City, OK, 73104, USA.
Geroscience. 2019 Oct;41(5):691-708. doi: 10.1007/s11357-019-00090-2. Epub 2019 Sep 7.
The systemic delivery of tamoxifen (Tam) to activate inducible CreERT2-loxP transgenic mouse systems is now widely used in neuroscience studies. This critical technological advancement allows temporal control of DNA-cre recombination, avoidance of embryonically lethal phenotypes, and minimization of residual cell labeling encountered in constitutively active drivers. Despite its advantages, the use of Tam has the potential to cause long-lasting, uncharacterized side effects on the transcriptome and epigenome in the CNS, given its mixed estrogen receptor (ER) agonist/antagonist actions. With the welcome focus on including both sexes in biomedical studies and efforts to understand sex differences, Tam administration could also cause sexually divergent responses that would confound studies. To examine these issues, epigenetic and transcriptomic profiles were compared in C57BL/6 J female and male hippocampus, cortex, and retina 1 month after a 5-day Tam treatment typical for cre induction, or vehicle control (sunflower seed oil). Cytosine methylation and hydroxymethylation levels, in both CG and non-CG contexts, were unchanged as determined by oxidative bisulfite sequencing. Long-lasting Tam transcriptomic effects were also not evident/minimal. Furthermore, there is no evidence of sexually divergent responses with Tam administration and Tam did not alter sex differences evident in controls. Combined with recently reported data that Tam alone does not cause long-lasting changes in behavior and neurogenesis, our findings provide confidence that Tam can be used as a cre-recombinase inducer without introducing significant confounds in transcriptomic and epigenomic neuroscience studies, particularly those focused on genomic and transcriptomic aspects of the aging brain.
他莫昔芬(Tam)的全身递送被广泛用于神经科学研究中的诱导型 CreERT2-loxP 转基因小鼠系统。这一关键技术进步允许对 DNA-cre 重组进行时间控制,避免胚胎致死表型,并最小化在组成性激活驱动剂中遇到的残留细胞标记。尽管具有优势,但鉴于他莫昔芬具有混合雌激素受体(ER)激动剂/拮抗剂作用,它有可能对中枢神经系统中的转录组和表观基因组产生持久的、未被描述的副作用。随着人们欢迎将男女两性纳入生物医学研究并努力了解性别差异,他莫昔芬给药也可能导致性别差异反应,从而混淆研究。为了研究这些问题,在 C57BL/6J 雌性和雄性海马体、皮层和视网膜中比较了 1 个月后经过 5 天他莫昔芬治疗(典型的 cre 诱导)或载体对照(葵花籽油)后的表观遗传组和转录组谱。通过氧化亚硫酸氢盐测序确定,CG 和非 CG 背景中的胞嘧啶甲基化和羟甲基化水平没有变化。长期的他莫昔芬转录组效应也不明显/最小。此外,没有证据表明他莫昔芬给药存在性别差异反应,并且他莫昔芬没有改变对照中明显的性别差异。与最近报道的他莫昔芬单独使用不会导致行为和神经发生的持久变化的数据相结合,我们的发现提供了信心,即他莫昔芬可以用作 cre 重组酶诱导剂,而不会在转录组和表观基因组神经科学研究中引入重大混淆,特别是那些专注于衰老大脑的基因组和转录组方面的研究。