Lopez Andrew L, Wang Shang, Larin Kirill V, Overbeek Paul A, Larina Irina V
Baylor College of Medicine, Department of Molecular Physiology and Biophysics, One Baylor Plaza, Houston 77030, United States.
Baylor College of Medicine, Department of Molecular Physiology and Biophysics, One Baylor Plaza, Houston 77030, United StatesbUniversity of Houston, Department of Biomedical Engineering, 3605 Cullen Boulevard, Houston 77204, United StatescSamara State Aer.
J Biomed Opt. 2015;20(9):090501. doi: 10.1117/1.JBO.20.9.090501.
Efficient phenotyping of developmental defects in model organisms is critical for understanding the genetic specification of normal development and congenital abnormalities in humans. We previously reported that optical coherence tomography (OCT) combined with live embryo culture is a valuable tool for mouse embryo imaging and four-dimensional (4-D) cardiodynamic analysis; however, its capability for analysis of mouse mutants with cardiac phenotypes has not been previously explored. Here, we report 4-D (three-dimensional+time) OCT imaging and analysis of the embryonic heart in a Wdr19 mouse mutant, revealing a heart looping defect. Quantitative analysis of cardiac looping revealed a statistically significant difference between mutant and control embryos. Our results indicate that live 4-D OCT imaging provides a powerful phenotyping approach to characterize embryonic cardiac function in mouse models.
在模式生物中对发育缺陷进行高效表型分析,对于理解人类正常发育和先天性异常的基因调控至关重要。我们之前报道过,光学相干断层扫描(OCT)结合活体胚胎培养是用于小鼠胚胎成像和四维(4-D)心脏动力学分析的一种有价值的工具;然而,其分析具有心脏表型的小鼠突变体的能力此前尚未被探索。在此,我们报告了对Wdr19小鼠突变体胚胎心脏的四维(三维+时间)OCT成像及分析,揭示了心脏环化缺陷。对心脏环化的定量分析显示,突变体胚胎与对照胚胎之间存在统计学上的显著差异。我们的结果表明,实时四维OCT成像为表征小鼠模型中的胚胎心脏功能提供了一种强大的表型分析方法。