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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Main Authors: Philip Heraud, Katarzyna Maria Marzec, Qing‒Hua Zhang, Wai Shan Yuen, John Carroll, Bayden R. Wood
Format: Article
Language:English
Published: Nature Publishing Group 2017-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-08973-0
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spelling 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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