Systematic assessment of variability in the proteome of iPSC derivatives

The use of induced pluripotent stem cells (iPSC) to model human complex diseases is gaining popularity as it allows investigation of human cells that are otherwise sparsely available. However, due to its laborious and cost intensive nature, iPSC research is often plagued by limited sample size and p...

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Main Authors: Stephanie D. Beekhuis-Hoekstra, Kyoko Watanabe, Josefin Werme, Christiaan A. de Leeuw, Iryna Paliukhovich, Ka Wan Li, Frank Koopmans, August B. Smit, Danielle Posthuma, Vivi M. Heine
Format: Article
Language:English
Published: Elsevier 2021-10-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506121003597
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spelling doaj-17cd00d645064ceab99c936775f4a01d2021-08-28T04:42:46ZengElsevierStem Cell Research1873-50612021-10-0156102512Systematic assessment of variability in the proteome of iPSC derivativesStephanie D. Beekhuis-Hoekstra0Kyoko Watanabe1Josefin Werme2Christiaan A. de Leeuw3Iryna Paliukhovich4Ka Wan Li5Frank Koopmans6August B. Smit7Danielle Posthuma8Vivi M. Heine9Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The NetherlandsDepartment of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The NetherlandsDepartment of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The NetherlandsDepartment of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The NetherlandsDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The NetherlandsDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The NetherlandsDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The NetherlandsDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The NetherlandsDepartment of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The Netherlands; Department of Child and Youth Psychiatry, Emma Children’s Hospital, Amsterdam Neuroscience, Amsterdam UMC, Amsterdam, The Netherlands; Corresponding authors at: Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The Netherlands.Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The Netherlands; Department of Child and Youth Psychiatry, Emma Children’s Hospital, Amsterdam Neuroscience, Amsterdam UMC, Amsterdam, The Netherlands; Corresponding authors at: Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, The Netherlands.The use of induced pluripotent stem cells (iPSC) to model human complex diseases is gaining popularity as it allows investigation of human cells that are otherwise sparsely available. However, due to its laborious and cost intensive nature, iPSC research is often plagued by limited sample size and putative large variability between clones, decreasing statistical power for detecting experimental effects. Here, we investigate the source and magnitude of variability in the proteome of parallel differentiated astrocytes using mass spectrometry. We compare three possible sources of variability: inter-donor variability, inter- and intra-clonal variability, at different stages of maturation. We show that the interclonal variability is significantly smaller than the inter-donor variability, and that including more donors has a much larger influence on statistical power than adding more clones per donor. Our results provide insight into the sources of variability at protein level between iPSC samples derived in parallel and will aid in optimizing iPSC studies.http://www.sciencedirect.com/science/article/pii/S1873506121003597
collection DOAJ
language English
format Article
sources DOAJ
author Stephanie D. Beekhuis-Hoekstra
Kyoko Watanabe
Josefin Werme
Christiaan A. de Leeuw
Iryna Paliukhovich
Ka Wan Li
Frank Koopmans
August B. Smit
Danielle Posthuma
Vivi M. Heine
spellingShingle Stephanie D. Beekhuis-Hoekstra
Kyoko Watanabe
Josefin Werme
Christiaan A. de Leeuw
Iryna Paliukhovich
Ka Wan Li
Frank Koopmans
August B. Smit
Danielle Posthuma
Vivi M. Heine
Systematic assessment of variability in the proteome of iPSC derivatives
Stem Cell Research
author_facet Stephanie D. Beekhuis-Hoekstra
Kyoko Watanabe
Josefin Werme
Christiaan A. de Leeuw
Iryna Paliukhovich
Ka Wan Li
Frank Koopmans
August B. Smit
Danielle Posthuma
Vivi M. Heine
author_sort Stephanie D. Beekhuis-Hoekstra
title Systematic assessment of variability in the proteome of iPSC derivatives
title_short Systematic assessment of variability in the proteome of iPSC derivatives
title_full Systematic assessment of variability in the proteome of iPSC derivatives
title_fullStr Systematic assessment of variability in the proteome of iPSC derivatives
title_full_unstemmed Systematic assessment of variability in the proteome of iPSC derivatives
title_sort systematic assessment of variability in the proteome of ipsc derivatives
publisher Elsevier
series Stem Cell Research
issn 1873-5061
publishDate 2021-10-01
description The use of induced pluripotent stem cells (iPSC) to model human complex diseases is gaining popularity as it allows investigation of human cells that are otherwise sparsely available. However, due to its laborious and cost intensive nature, iPSC research is often plagued by limited sample size and putative large variability between clones, decreasing statistical power for detecting experimental effects. Here, we investigate the source and magnitude of variability in the proteome of parallel differentiated astrocytes using mass spectrometry. We compare three possible sources of variability: inter-donor variability, inter- and intra-clonal variability, at different stages of maturation. We show that the interclonal variability is significantly smaller than the inter-donor variability, and that including more donors has a much larger influence on statistical power than adding more clones per donor. Our results provide insight into the sources of variability at protein level between iPSC samples derived in parallel and will aid in optimizing iPSC studies.
url http://www.sciencedirect.com/science/article/pii/S1873506121003597
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