The Quantitative Proteomes of Human-induced Pluripotent Stem Cells and Embryonic Stem Cells
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Assessing relevant molecular differences between human-induced pluripotent stem cells (hiPSCs) and human embryonic stem cells (hESCs) is important, given that such differences may impact their potential therapeutic use. Controversy surrounds recent gene expression studies comparing hiPSCs and hESCs. Here, we present an in-depth quantitative mass spectrometry-based analysis of hESCs, two different hiPSCs and their precursor fibroblast cell lines. Our comparisons confirmed the high similarity of hESCs and hiPSCS at the proteome level as 97.8% of the proteins were found unchanged. Nevertheless, a small group of 58 proteins, mainly related to metabolism, antigen processing and cell adhesion, was found significantly differentially expressed between hiPSCs and hESCs. A comparison of the regulated proteins with previously published transcriptomic studies showed a low overlap, highlighting the emerging notion that differences between both pluripotent cell lines rather reflect experimental conditions than a recurrent molecular signature.
Proteomic and functional comparison between human induced and embryonic stem cells.
Brenes A, Griesser E, Sinclair L, Davidson L, Prescott A, Singh F Elife. 2024; 13.
PMID: 39540879 PMC: 11563575. DOI: 10.7554/eLife.92025.
A secreted proteomic footprint for stem cell pluripotency.
Lewis P, Silajdzic E, Smith H, Bates N, Smith C, Mancini F PLoS One. 2024; 19(6):e0299365.
PMID: 38875182 PMC: 11178176. DOI: 10.1371/journal.pone.0299365.
Profiling the role of m6A effectors in the regulation of pluripotent reprogramming.
Wang W, Zhou L, Li H, Sun T, Wen X, Li W Hum Genomics. 2024; 18(1):33.
PMID: 38566168 PMC: 10986062. DOI: 10.1186/s40246-024-00597-6.
Proteomics applications in next generation induced pluripotent stem cell models.
Manda V, Pavelka J, Lau E Expert Rev Proteomics. 2024; 21(4):217-228.
PMID: 38511670 PMC: 11065590. DOI: 10.1080/14789450.2024.2334033.
Durand S, Bruelle M, Bourdelais F, Bennychen B, Blin-Gonthier J, Isaac C Nat Commun. 2023; 14(1):356.
PMID: 36690642 PMC: 9870888. DOI: 10.1038/s41467-023-36037-7.