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Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model

Adipose tissue is the primary tissue affected in most single gene forms of severe insulin resistance, and growing evidence has implicated it as a site at which many risk alleles for insulin resistance identified in population-wide studies might exert their effect. There is thus increasing need for h...

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Autores principales: Chen, Jian-Hua, Goh, Kim Jee, Rocha, Nuno, Groeneveld, Matthijs P., Minic, Marina, Barrett, Timothy G., Savage, David, Semple, Robert K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769609/
https://www.ncbi.nlm.nih.gov/pubmed/28982679
http://dx.doi.org/10.1242/dmm.030981
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author Chen, Jian-Hua
Goh, Kim Jee
Rocha, Nuno
Groeneveld, Matthijs P.
Minic, Marina
Barrett, Timothy G.
Savage, David
Semple, Robert K.
author_facet Chen, Jian-Hua
Goh, Kim Jee
Rocha, Nuno
Groeneveld, Matthijs P.
Minic, Marina
Barrett, Timothy G.
Savage, David
Semple, Robert K.
author_sort Chen, Jian-Hua
collection PubMed
description Adipose tissue is the primary tissue affected in most single gene forms of severe insulin resistance, and growing evidence has implicated it as a site at which many risk alleles for insulin resistance identified in population-wide studies might exert their effect. There is thus increasing need for human adipocyte models in which to interrogate the function of known and emerging genetic risk variants. However, primary adipocyte cultures, existing immortalised cell lines and stem-cell based models all have significant biological or practical limitations. In an attempt to widen the repertoire of human cell models in which to study adipocyte-autonomous effects of relevant human genetic variants, we have undertaken direct reprogramming of skin fibroblasts to adipocyte-like cells by employing an inducible recombinant lentivirus overexpressing the master adipogenic transcription factor PPARγ2. Doxycycline-driven expression of PPARγ2 and adipogenic culture conditions converted dermal fibroblasts into triglyceride-laden cells within days. The resulting cells recapitulated most of the crucial aspects of adipocyte biology in vivo, including the expression of mature adipocyte markers, secreted high levels of the adipokine adiponectin, and underwent lipolysis when treated with isoproterenol/3-isobutyl-1-methylxanthine (IBMX). They did not, however, exhibit insulin-inducible glucose uptake, and withdrawal of doxycycline produced rapid delipidation and loss of adipogenic markers. This protocol was applied successfully to a panel of skin cells from individuals with monogenic severe insulin resistance; however, surprisingly, even cell lines harbouring mutations causing severe, generalised lipodystrophy accumulated large lipid droplets and induced adipocyte-specific genes. The direct reprogramming protocol of human dermal fibroblasts to adipocyte-like cells we established is simple, fast and efficient, and has the potential to generate cells which can serve as a tool to address some, though not all, aspects of adipocyte function in the presence of endogenous disease-causing mutations.
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spelling pubmed-57696092018-01-19 Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model Chen, Jian-Hua Goh, Kim Jee Rocha, Nuno Groeneveld, Matthijs P. Minic, Marina Barrett, Timothy G. Savage, David Semple, Robert K. Dis Model Mech Research Article Adipose tissue is the primary tissue affected in most single gene forms of severe insulin resistance, and growing evidence has implicated it as a site at which many risk alleles for insulin resistance identified in population-wide studies might exert their effect. There is thus increasing need for human adipocyte models in which to interrogate the function of known and emerging genetic risk variants. However, primary adipocyte cultures, existing immortalised cell lines and stem-cell based models all have significant biological or practical limitations. In an attempt to widen the repertoire of human cell models in which to study adipocyte-autonomous effects of relevant human genetic variants, we have undertaken direct reprogramming of skin fibroblasts to adipocyte-like cells by employing an inducible recombinant lentivirus overexpressing the master adipogenic transcription factor PPARγ2. Doxycycline-driven expression of PPARγ2 and adipogenic culture conditions converted dermal fibroblasts into triglyceride-laden cells within days. The resulting cells recapitulated most of the crucial aspects of adipocyte biology in vivo, including the expression of mature adipocyte markers, secreted high levels of the adipokine adiponectin, and underwent lipolysis when treated with isoproterenol/3-isobutyl-1-methylxanthine (IBMX). They did not, however, exhibit insulin-inducible glucose uptake, and withdrawal of doxycycline produced rapid delipidation and loss of adipogenic markers. This protocol was applied successfully to a panel of skin cells from individuals with monogenic severe insulin resistance; however, surprisingly, even cell lines harbouring mutations causing severe, generalised lipodystrophy accumulated large lipid droplets and induced adipocyte-specific genes. The direct reprogramming protocol of human dermal fibroblasts to adipocyte-like cells we established is simple, fast and efficient, and has the potential to generate cells which can serve as a tool to address some, though not all, aspects of adipocyte function in the presence of endogenous disease-causing mutations. The Company of Biologists Ltd 2017-12-01 /pmc/articles/PMC5769609/ /pubmed/28982679 http://dx.doi.org/10.1242/dmm.030981 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Chen, Jian-Hua
Goh, Kim Jee
Rocha, Nuno
Groeneveld, Matthijs P.
Minic, Marina
Barrett, Timothy G.
Savage, David
Semple, Robert K.
Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model
title Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model
title_full Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model
title_fullStr Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model
title_full_unstemmed Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model
title_short Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model
title_sort evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769609/
https://www.ncbi.nlm.nih.gov/pubmed/28982679
http://dx.doi.org/10.1242/dmm.030981
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