Protocol to image, segment, and quantify cortical contractions in maturing mouse oocytes

Summary: Mouse oocytes devoid of branched actin display prolonged cortical contractions during the first meiotic division. Here, we present a protocol to collect fully grown oocytes in prophase I arrest and record their contractions during the first meiotic division through time-lapse imaging in tra...

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Main Authors: Gaëlle Letort, Elvira Nikalayevich
Format: Article
Language:English
Published: Elsevier 2025-03-01
Series:STAR Protocols
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666166725000103
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author Gaëlle Letort
Elvira Nikalayevich
author_facet Gaëlle Letort
Elvira Nikalayevich
author_sort Gaëlle Letort
collection DOAJ
description Summary: Mouse oocytes devoid of branched actin display prolonged cortical contractions during the first meiotic division. Here, we present a protocol to collect fully grown oocytes in prophase I arrest and record their contractions during the first meiotic division through time-lapse imaging in transillumination, without additional labeling. We then explain how to set up the pipeline to segment the oocyte outline with an ImageJ plugin Oocytor and to measure cortical fluctuations with the help of an ImageJ plugin Radioak.For complete details on the use and execution of this protocol, please refer to Nikalayevich et al.1 : Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.
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series STAR Protocols
spelling doaj-art-f4ffb78555d14d8ba5c69ed773cf06412025-01-31T05:12:25ZengElsevierSTAR Protocols2666-16672025-03-0161103604Protocol to image, segment, and quantify cortical contractions in maturing mouse oocytesGaëlle Letort0Elvira Nikalayevich1Department of Developmental and Stem Cell Biology, Institut Pasteur, CNRS UMR 3738, Université Paris Cité, 25 Rue du Dr. Roux, 75015 Paris, France; Corresponding authorCenter for Interdisciplinary Research in Biology (CIRB), Collège de France, Université PSL, CNRS, INSERM, 75005 Paris, France; Corresponding authorSummary: Mouse oocytes devoid of branched actin display prolonged cortical contractions during the first meiotic division. Here, we present a protocol to collect fully grown oocytes in prophase I arrest and record their contractions during the first meiotic division through time-lapse imaging in transillumination, without additional labeling. We then explain how to set up the pipeline to segment the oocyte outline with an ImageJ plugin Oocytor and to measure cortical fluctuations with the help of an ImageJ plugin Radioak.For complete details on the use and execution of this protocol, please refer to Nikalayevich et al.1 : Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.http://www.sciencedirect.com/science/article/pii/S2666166725000103cell culturesingle celldevelopmental biologymicroscopy
spellingShingle Gaëlle Letort
Elvira Nikalayevich
Protocol to image, segment, and quantify cortical contractions in maturing mouse oocytes
STAR Protocols
cell culture
single cell
developmental biology
microscopy
title Protocol to image, segment, and quantify cortical contractions in maturing mouse oocytes
title_full Protocol to image, segment, and quantify cortical contractions in maturing mouse oocytes
title_fullStr Protocol to image, segment, and quantify cortical contractions in maturing mouse oocytes
title_full_unstemmed Protocol to image, segment, and quantify cortical contractions in maturing mouse oocytes
title_short Protocol to image, segment, and quantify cortical contractions in maturing mouse oocytes
title_sort protocol to image segment and quantify cortical contractions in maturing mouse oocytes
topic cell culture
single cell
developmental biology
microscopy
url http://www.sciencedirect.com/science/article/pii/S2666166725000103
work_keys_str_mv AT gaelleletort protocoltoimagesegmentandquantifycorticalcontractionsinmaturingmouseoocytes
AT elviranikalayevich protocoltoimagesegmentandquantifycorticalcontractionsinmaturingmouseoocytes