Time-lapse mechanical imaging of neural tube closure in live embryo using Brillouin microscopy
Abstract 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 l...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2023-01-01
|
Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-023-27456-z |
_version_ | 1797958705532108800 |
---|---|
author | Chenchen Handler Giuliano Scarcelli Jitao Zhang |
author_facet | Chenchen Handler Giuliano Scarcelli Jitao Zhang |
author_sort | Chenchen Handler |
collection | DOAJ |
description | Abstract 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. |
first_indexed | 2024-04-11T00:22:48Z |
format | Article |
id | doaj.art-5172c08345d243c3b599c6a875f018dd |
institution | Directory Open Access Journal |
issn | 2045-2322 |
language | English |
last_indexed | 2024-04-11T00:22:48Z |
publishDate | 2023-01-01 |
publisher | Nature Portfolio |
record_format | Article |
series | Scientific Reports |
spelling | doaj.art-5172c08345d243c3b599c6a875f018dd2023-01-08T12:10:47ZengNature PortfolioScientific Reports2045-23222023-01-011311810.1038/s41598-023-27456-zTime-lapse mechanical imaging of neural tube closure in live embryo using Brillouin microscopyChenchen Handler0Giuliano Scarcelli1Jitao Zhang2Fischell Department of Bioengineering, A. James Clark School of Engineering, University of MarylandFischell Department of Bioengineering, A. James Clark School of Engineering, University of MarylandDepartment of Biomedical Engineering, Wayne State UniversityAbstract 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.https://doi.org/10.1038/s41598-023-27456-z |
spellingShingle | Chenchen Handler Giuliano Scarcelli Jitao Zhang Time-lapse mechanical imaging of neural tube closure in live embryo using Brillouin microscopy Scientific Reports |
title | Time-lapse mechanical imaging of neural tube closure in live embryo using Brillouin microscopy |
title_full | Time-lapse mechanical imaging of neural tube closure in live embryo using Brillouin microscopy |
title_fullStr | Time-lapse mechanical imaging of neural tube closure in live embryo using Brillouin microscopy |
title_full_unstemmed | Time-lapse mechanical imaging of neural tube closure in live embryo using Brillouin microscopy |
title_short | Time-lapse mechanical imaging of neural tube closure in live embryo using Brillouin microscopy |
title_sort | time lapse mechanical imaging of neural tube closure in live embryo using brillouin microscopy |
url | https://doi.org/10.1038/s41598-023-27456-z |
work_keys_str_mv | AT chenchenhandler timelapsemechanicalimagingofneuraltubeclosureinliveembryousingbrillouinmicroscopy AT giulianoscarcelli timelapsemechanicalimagingofneuraltubeclosureinliveembryousingbrillouinmicroscopy AT jitaozhang timelapsemechanicalimagingofneuraltubeclosureinliveembryousingbrillouinmicroscopy |