Proteomic and functional comparison between human induced and embryonic stem cells

Human induced pluripotent stem cells (hiPSCs) have great potential to be used as alternatives to embryonic stem cells (hESCs) in regenerative medicine and disease modelling. In this study, we characterise the proteomes of multiple hiPSC and hESC lines derived from independent donors and find that while they express a near-identical set of proteins, they show consistent quantitative differences in the abundance of a subset of proteins. hiPSCs have increased total protein content, while maintaining a comparable cell cycle profile to hESCs, with increased abundance of cytoplasmic and mitochondrial proteins required to sustain high growth rates, including nutrient transporters and metabolic proteins. Prominent changes detected in proteins involved in mitochondrial metabolism correlated with enhanced mitochondrial potential, shown using high-resolution respirometry. hiPSCs also produced higher levels of secreted proteins, including growth factors and proteins involved in the inhibition of the immune system. The data indicate that reprogramming of fibroblasts to hiPSCs produces important differences in cytoplasmic and mitochondrial proteins compared to hESCs, with consequences affecting growth and metabolism. This study improves our understanding of the molecular differences between hiPSCs and hESCs, with implications for potential risks and benefits for their use in future disease modelling and therapeutic applications.

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Publication Details

Journal
eLife
Published
2024-10-28
DOI
https://doi.org/10.7554/elife.92025.3
Citations
3
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
0.70

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article

Proteomic and functional comparison between human induced and embryonic stem cells

Melpomeni Platani, Angus I. Lamond, L. S. P. Davidson, Greg M. Findlay et al.
3 citations
eLife
Pluripotent Stem Cells Research
0.70
article

Proteomic and functional comparison between human induced and embryonic stem cells

Melpomeni Platani, Angus I. Lamond, L. S. P. Davidson, Greg M. Findlay, Doreen A. Cantrell, Harunori Yoshikawa, Carmen Espejo-Serrano, Alan R. Prescott, Eva Griesser, Alejandro J. Brenes, Elizabeth Hogg, François Singh, Linda V. Sinclair, Jason R. Swedlow, Hao Jiang
article en
3 citations

Abstract

Human induced pluripotent stem cells (hiPSCs) have great potential to be used as alternatives to embryonic stem cells (hESCs) in regenerative medicine and disease modelling. In this study, we characterise the proteomes of multiple hiPSC and hESC lines derived from independent donors and find that while they express a near-identical set of proteins, they show consistent quantitative differences in the abundance of a subset of proteins. hiPSCs have increased total protein content, while maintaining a comparable cell cycle profile to hESCs, with increased abundance of cytoplasmic and mitochondrial proteins required to sustain high growth rates, including nutrient transporters and metabolic proteins. Prominent changes detected in proteins involved in mitochondrial metabolism correlated with enhanced mitochondrial potential, shown using high-resolution respirometry. hiPSCs also produced higher levels of secreted proteins, including growth factors and proteins involved in the inhibition of the immune system. The data indicate that reprogramming of fibroblasts to hiPSCs produces important differences in cytoplasmic and mitochondrial proteins compared to hESCs, with consequences affecting growth and metabolism. This study improves our understanding of the molecular differences between hiPSCs and hESCs, with implications for potential risks and benefits for their use in future disease modelling and therapeutic applications.

eLifeVol. 13
University of Dundee (GB), MRC Protein Phosphorylation and Ubiquitylation Unit (GB)
Wellcome Trust, Engineering and Physical Sciences Research Council, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 29%
Pluripotent Stem Cells Research
0.70
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