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Small Molecule Injection into Single-Cell C. elegans Embryos via Carbon-Reinforced Nanopipettes
The introduction of chemical inhibitors into living cells at specific times in development is a useful method for investigating the roles of specific proteins or cytoskeletal components in developmental processes. Some embryos, such as those of Caenorhabditis elegans, however, possess a tough eggshe...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784451/ https://www.ncbi.nlm.nih.gov/pubmed/24086620 http://dx.doi.org/10.1371/journal.pone.0075712 |
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author | Brennan, Lucy D. Roland, Thibault Morton, Diane G. Fellman, Shanna M. Chung, SueYeon Soltani, Mohammad Kevek, Joshua W. McEuen, Paul M. Kemphues, Kenneth J. Wang, Michelle D. |
author_facet | Brennan, Lucy D. Roland, Thibault Morton, Diane G. Fellman, Shanna M. Chung, SueYeon Soltani, Mohammad Kevek, Joshua W. McEuen, Paul M. Kemphues, Kenneth J. Wang, Michelle D. |
author_sort | Brennan, Lucy D. |
collection | PubMed |
description | The introduction of chemical inhibitors into living cells at specific times in development is a useful method for investigating the roles of specific proteins or cytoskeletal components in developmental processes. Some embryos, such as those of Caenorhabditis elegans, however, possess a tough eggshell that makes introducing drugs and other molecules into embryonic cells challenging. We have developed a procedure using carbon-reinforced nanopipettes (CRNPs) to deliver molecules into C. elegans embryos with high temporal control. The use of CRNPs allows for cellular manipulation to occur just subsequent to meiosis II with minimal damage to the embryo. We have used our technique to replicate classical experiments using latrunculin A to inhibit microfilaments and assess its effects on early polarity establishment. Our injections of latrunculin A confirm the necessity of microfilaments in establishing anterior-posterior polarity at this early stage, even when microtubules remain intact. Further, we find that latrunculin A treatment does not prevent association of PAR-2 or PAR-6 with the cell cortex. Our experiments demonstrate the application of carbon-reinforced nanopipettes to the study of one temporally-confined developmental event. The use of CRNPs to introduce molecules into the embryo should be applicable to investigations at later developmental stages as well as other cells with tough outer coverings. |
format | Online Article Text |
id | pubmed-3784451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37844512013-10-01 Small Molecule Injection into Single-Cell C. elegans Embryos via Carbon-Reinforced Nanopipettes Brennan, Lucy D. Roland, Thibault Morton, Diane G. Fellman, Shanna M. Chung, SueYeon Soltani, Mohammad Kevek, Joshua W. McEuen, Paul M. Kemphues, Kenneth J. Wang, Michelle D. PLoS One Research Article The introduction of chemical inhibitors into living cells at specific times in development is a useful method for investigating the roles of specific proteins or cytoskeletal components in developmental processes. Some embryos, such as those of Caenorhabditis elegans, however, possess a tough eggshell that makes introducing drugs and other molecules into embryonic cells challenging. We have developed a procedure using carbon-reinforced nanopipettes (CRNPs) to deliver molecules into C. elegans embryos with high temporal control. The use of CRNPs allows for cellular manipulation to occur just subsequent to meiosis II with minimal damage to the embryo. We have used our technique to replicate classical experiments using latrunculin A to inhibit microfilaments and assess its effects on early polarity establishment. Our injections of latrunculin A confirm the necessity of microfilaments in establishing anterior-posterior polarity at this early stage, even when microtubules remain intact. Further, we find that latrunculin A treatment does not prevent association of PAR-2 or PAR-6 with the cell cortex. Our experiments demonstrate the application of carbon-reinforced nanopipettes to the study of one temporally-confined developmental event. The use of CRNPs to introduce molecules into the embryo should be applicable to investigations at later developmental stages as well as other cells with tough outer coverings. Public Library of Science 2013-09-26 /pmc/articles/PMC3784451/ /pubmed/24086620 http://dx.doi.org/10.1371/journal.pone.0075712 Text en © 2013 Brennan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Brennan, Lucy D. Roland, Thibault Morton, Diane G. Fellman, Shanna M. Chung, SueYeon Soltani, Mohammad Kevek, Joshua W. McEuen, Paul M. Kemphues, Kenneth J. Wang, Michelle D. Small Molecule Injection into Single-Cell C. elegans Embryos via Carbon-Reinforced Nanopipettes |
title | Small Molecule Injection into Single-Cell C. elegans Embryos via Carbon-Reinforced Nanopipettes |
title_full | Small Molecule Injection into Single-Cell C. elegans Embryos via Carbon-Reinforced Nanopipettes |
title_fullStr | Small Molecule Injection into Single-Cell C. elegans Embryos via Carbon-Reinforced Nanopipettes |
title_full_unstemmed | Small Molecule Injection into Single-Cell C. elegans Embryos via Carbon-Reinforced Nanopipettes |
title_short | Small Molecule Injection into Single-Cell C. elegans Embryos via Carbon-Reinforced Nanopipettes |
title_sort | small molecule injection into single-cell c. elegans embryos via carbon-reinforced nanopipettes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784451/ https://www.ncbi.nlm.nih.gov/pubmed/24086620 http://dx.doi.org/10.1371/journal.pone.0075712 |
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