Label-free in vivo Raman microspectroscopic imaging of the macromolecular architecture of oocytes
Abstract Confocal Raman spectroscopy (CRS) can provide information about oocyte competency through measurement of changes in the macromolecular architecture during oocyte development and maturation. Hitherto most spectroscopic studies have been limited to fixed oocytes due to the inherent difficulti...
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2017-08-01
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doaj-11ddf29393e94723aff040e434d0454c2020-12-08T01:38:01ZengNature Publishing GroupScientific Reports2045-23222017-08-017111010.1038/s41598-017-08973-0Label-free in vivo Raman microspectroscopic imaging of the macromolecular architecture of oocytesPhilip Heraud0Katarzyna Maria Marzec1Qing‒Hua Zhang2Wai Shan Yuen3John Carroll4Bayden R. Wood5Centre for Biospectroscopy, School of Chemistry, Monash University, ClaytonJagiellonian Centre for Experimental Therapeutics (JCET), Jagiellonian UniversityDepartment of Microbiology, Monash University, ClaytonDepartment of Microbiology, Monash University, ClaytonDepartment of Microbiology, Monash University, ClaytonCentre for Biospectroscopy, School of Chemistry, Monash University, ClaytonAbstract Confocal Raman spectroscopy (CRS) can provide information about oocyte competency through measurement of changes in the macromolecular architecture during oocyte development and maturation. Hitherto most spectroscopic studies have been limited to fixed oocytes due to the inherent difficulties working with live cells. Here we report the first three-dimensional images of living murine oocytes using CRS. We show that fixation induces significant changes in the macromolecular chemistry compared to living oocytes. A band at 1602 cm−1, assigned to a marker for mitochondria function was found in living oocytes but absent from fixed oocytes providing an in vivo marker. Fixation resulted in significant changes in protein and nucleic acid bands and the spatial distribution of organelles. Raman imaging of Metaphase I and II (MI, MII) and germinal vesicle stage oocytes showed changes in nuclear organisation and cytoplasm macromolecular architecture during these development and maturation stages related to changes in chromosome condensation, mitochondria aggregation and lipid droplet numbers.https://doi.org/10.1038/s41598-017-08973-0 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Philip Heraud Katarzyna Maria Marzec Qing‒Hua Zhang Wai Shan Yuen John Carroll Bayden R. Wood |
spellingShingle |
Philip Heraud Katarzyna Maria Marzec Qing‒Hua Zhang Wai Shan Yuen John Carroll Bayden R. Wood Label-free in vivo Raman microspectroscopic imaging of the macromolecular architecture of oocytes Scientific Reports |
author_facet |
Philip Heraud Katarzyna Maria Marzec Qing‒Hua Zhang Wai Shan Yuen John Carroll Bayden R. Wood |
author_sort |
Philip Heraud |
title |
Label-free in vivo Raman microspectroscopic imaging of the macromolecular architecture of oocytes |
title_short |
Label-free in vivo Raman microspectroscopic imaging of the macromolecular architecture of oocytes |
title_full |
Label-free in vivo Raman microspectroscopic imaging of the macromolecular architecture of oocytes |
title_fullStr |
Label-free in vivo Raman microspectroscopic imaging of the macromolecular architecture of oocytes |
title_full_unstemmed |
Label-free in vivo Raman microspectroscopic imaging of the macromolecular architecture of oocytes |
title_sort |
label-free in vivo raman microspectroscopic imaging of the macromolecular architecture of oocytes |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-08-01 |
description |
Abstract Confocal Raman spectroscopy (CRS) can provide information about oocyte competency through measurement of changes in the macromolecular architecture during oocyte development and maturation. Hitherto most spectroscopic studies have been limited to fixed oocytes due to the inherent difficulties working with live cells. Here we report the first three-dimensional images of living murine oocytes using CRS. We show that fixation induces significant changes in the macromolecular chemistry compared to living oocytes. A band at 1602 cm−1, assigned to a marker for mitochondria function was found in living oocytes but absent from fixed oocytes providing an in vivo marker. Fixation resulted in significant changes in protein and nucleic acid bands and the spatial distribution of organelles. Raman imaging of Metaphase I and II (MI, MII) and germinal vesicle stage oocytes showed changes in nuclear organisation and cytoplasm macromolecular architecture during these development and maturation stages related to changes in chromosome condensation, mitochondria aggregation and lipid droplet numbers. |
url |
https://doi.org/10.1038/s41598-017-08973-0 |
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