Projects per year
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.
Original language | English |
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Pages (from-to) | 1-32 |
Number of pages | 32 |
Journal | eLife |
Volume | 13 |
DOIs | |
Publication status | Published - 14 Nov 2024 |
Keywords
- proteomics
- iPSC
- mass spectrometry
- hESC
- TMT
- stem cells
- protein content
- chemical biology
- stem cell
- regenerative medicine
- biochemistry
- human
ASJC Scopus subject areas
- General Neuroscience
- General Biochemistry,Genetics and Molecular Biology
- General Immunology and Microbiology
Fingerprint
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Harnessing the splicing code for targeted control of gene expression (UNLEASH)
Gray, D. (Investigator) & Lamond, A. (Investigator)
1/06/23 → 31/05/29
Project: Research
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Molecular Analysis of Nuclear Bodies and RNP Trafficking Pathways in the Cell Nucleus (Joint with the University of Oslo)
Lamond, A. (Investigator)
Biotechnology and Biological Sciences Research Council
1/05/21 → 30/04/25
Project: Research
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The Interplay Between Oxygen Sensors PHDs and the Cell Cycle (Joint with University of Liverpool)
Fleming, S. (Investigator), Lamond, A. (Investigator) & Swedlow, J. (Investigator)
1/09/17 → 31/08/24
Project: Research
Research output
- 1 Citations
- 1 Preprint
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Proteomic and functional comparison between human induced and embryonic stem cells
Brenes Murillo, A., Griesser, E., Sinclair, L., Davidson, L., Prescott, A., Singh, F., Hogg, E., Espejo-Serrano, C., Jiang, H., Yoshikawa, H., Platani, M., Swedlow, J., Findlay, G., Cantrell, D. & Lamond, A. (Lead / Corresponding author), 19 Aug 2023, BioRxiv, 34 p.Research output: Working paper/Preprint › Preprint
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