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Spatiotemporal Labeling of Melanocytes in Mice

Melanocytes are pigment producing cells in the skin that give rise to cutaneous malignant melanoma, which is a highly aggressive and the deadliest form of skin cancer. Studying melanocytes in vivo is often difficult due to their small proportion in the skin and the lack of specific cell surface mark...

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Autores principales: Preston, Sarah, Aras, Shweta, Zaidi, M. Raza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5983676/
https://www.ncbi.nlm.nih.gov/pubmed/29762513
http://dx.doi.org/10.3390/ijms19051469
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author Preston, Sarah
Aras, Shweta
Zaidi, M. Raza
author_facet Preston, Sarah
Aras, Shweta
Zaidi, M. Raza
author_sort Preston, Sarah
collection PubMed
description Melanocytes are pigment producing cells in the skin that give rise to cutaneous malignant melanoma, which is a highly aggressive and the deadliest form of skin cancer. Studying melanocytes in vivo is often difficult due to their small proportion in the skin and the lack of specific cell surface markers. Several genetically-engineered mouse models (GEMMs) have been created to specifically label the melanocyte compartment. These models give both spatial and temporal control over the expression of a cellular ‘beacon’ that has an added benefit of inducible expression that can be activated on demand. Two powerful models that are discussed in this review include the melanocyte-specific, tetracycline-inducible green fluorescent protein expression system (iDct-GFP), and the fluorescent ubiquitination-based cell cycle indicator (FUCCI) model that allows for the monitoring of the cell-cycle. These two systems are powerful tools in studying melanocyte and melanoma biology. We discuss their current uses and how they could be employed to help answer unresolved questions in the fields of melanocyte and melanoma biology.
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spelling pubmed-59836762018-06-05 Spatiotemporal Labeling of Melanocytes in Mice Preston, Sarah Aras, Shweta Zaidi, M. Raza Int J Mol Sci Review Melanocytes are pigment producing cells in the skin that give rise to cutaneous malignant melanoma, which is a highly aggressive and the deadliest form of skin cancer. Studying melanocytes in vivo is often difficult due to their small proportion in the skin and the lack of specific cell surface markers. Several genetically-engineered mouse models (GEMMs) have been created to specifically label the melanocyte compartment. These models give both spatial and temporal control over the expression of a cellular ‘beacon’ that has an added benefit of inducible expression that can be activated on demand. Two powerful models that are discussed in this review include the melanocyte-specific, tetracycline-inducible green fluorescent protein expression system (iDct-GFP), and the fluorescent ubiquitination-based cell cycle indicator (FUCCI) model that allows for the monitoring of the cell-cycle. These two systems are powerful tools in studying melanocyte and melanoma biology. We discuss their current uses and how they could be employed to help answer unresolved questions in the fields of melanocyte and melanoma biology. MDPI 2018-05-15 /pmc/articles/PMC5983676/ /pubmed/29762513 http://dx.doi.org/10.3390/ijms19051469 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Preston, Sarah
Aras, Shweta
Zaidi, M. Raza
Spatiotemporal Labeling of Melanocytes in Mice
title Spatiotemporal Labeling of Melanocytes in Mice
title_full Spatiotemporal Labeling of Melanocytes in Mice
title_fullStr Spatiotemporal Labeling of Melanocytes in Mice
title_full_unstemmed Spatiotemporal Labeling of Melanocytes in Mice
title_short Spatiotemporal Labeling of Melanocytes in Mice
title_sort spatiotemporal labeling of melanocytes in mice
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5983676/
https://www.ncbi.nlm.nih.gov/pubmed/29762513
http://dx.doi.org/10.3390/ijms19051469
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