Time-lapse mechanical imaging of neural tube closure in live embryo using Brillouin microscopy

被引:15
|
作者
Handler, Chenchen [1 ]
Scarcelli, Giuliano [1 ]
Zhang, Jitao [2 ]
机构
[1] Univ Maryland, A James Clark Sch Engn, Fischell Dept Bioengn, College Pk, MD 20742 USA
[2] Wayne State Univ, Dept Biomed Engn, Detroit, MI 48201 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
SPECTROSCOPY MEASUREMENTS; WATER-CONTENT; CELL-SHAPE; NEURULATION; MIGRATION; STIFFNESS; DEFECTS; FORCES; FORM;
D O I
10.1038/s41598-023-27456-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neural tube closure (NTC) is a complex process of embryonic development involving molecular, cellular, and biomechanical mechanisms. While the genetic factors and biochemical signaling have been extensively investigated, the role of tissue biomechanics remains mostly unexplored due to the lack of tools. Here, we developed an optical modality that can conduct time-lapse mechanical imaging of neural plate tissue as the embryo is experiencing neurulation. This technique is based on the combination of a confocal Brillouin microscope and a modified ex ovo culturing of chick embryo with an on-stage incubator. With this technique, for the first time, we captured the mechanical evolution of the neural plate tissue with live embryos. Specifically, we observed the continuous increase in tissue modulus of the neural plate during NTC for ex ovo cultured embryos, which is consistent with the data of in ovo culture as well as previous studies. Beyond that, we found that the increase in tissue modulus was highly correlated with the tissue thickening and bending. We foresee this non-contact and label-free technique opening new opportunities to understand the biomechanical mechanisms in embryonic development.
引用
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页数:8
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