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Nature Communications. CNIO researchers describe how embryonic stem cells maintain optimal conditions for use in regenerative medicine


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Embryonic stem cells, CNIO Embryonic stem cells, in naïve state (left) and primed state (right). /CNIO

Researchers from the Proteomics Core Unit at CNIO have described molecular mechanisms, unknown to date, involved in the maintenance of the naïve state of the embryonic stem cells

The naïve state is optimal for the quest for treatments for heart disease or neurodegenerative disorders, but it is also the most unstable and difficult to maintain. The study by CNIO researchers may help obtain stable cell cultures that may last longer

The results of the study, which is published in ‘Nature Communications’, might prove useful to study some types of cancer

Scientists at the Proteomics Core Unit of the Spanish National Cancer Research Centre (CNIO), headed by Javier Muñoz, have described the mechanisms, unknown to date, involved in maintaining embryonic stem cells in the best possible state for their use in regenerative medicine. Their results, published in Nature Communications, will help to find novel stem-cell therapies for brain stroke, heart disease or neurodegenerative conditions like Alzheimer’s or Parkinson’s disease.

Naïve pluripotent stem cells, ideal for doing research

Embryonic stem cells (ESCs) are pluripotent cells that can grow into all somatic cell types – a characteristic that is extremely useful for researchers and regenerative medicine. There are two types of pluripotency: naïve and primed. The naïve state comes before the primed one during embryonic development. Naïve ESCs have the potential to differentiate into any cell types. Thus, they are more relevant in research. However, the naïve state is unstable, because naïve ESCs are constantly receiving signals that regulate the transition to the primed state and their self-renewal. Understanding the mechanisms that regulate the pluripotent states is important because they might help achieve long-term maintenance of stable naïve pluripotent stem cells in ESC cultures.

Traditionally, maintenance of naïve ESC cultures is based on the inhibition of two of the signalling pathways that regulate cell differentiation – aka as the 2i culture method. Recently, naïve ESCs have been maintained adopting a totally different approach, namely, the inhibition of Cdk8/19, a protein that regulates the expression of numerous genes, including the genes that help maintain the naïve state. “While the two approaches are used to culture naïve cells, little is known about the mechanisms involved,” says Javier Muñoz, who led the study.

Now, using proteomics, the large-scale characterisation of proteins coded in a genome, CNIO scientists have described a large number of the molecular events that help stabilise these valuable ESC. “This is the first time proteomics has been used in this context,” says Ana Martínez del Val, from the Proteomics Core Unit at CNIO, first author of the article. “We analysed the mechanisms at a number of levels. First, we conducted phosphoproteomic analyses, studying phosphorylated proteins. Phosphorylation regulates protein functions (by activating or inhibiting them). Second, we analysed the expression of these proteins. Finally, we identified changes in metabolites (reaction intermediates or end products). With our integrated approach, we got an accurate picture of the causes of the high degree of plasticity of ESC,” Martínez del Val explains.

The results of the study might have implications for research on some types of cancer. We know that “the inhibition of Cdk8 leads to reduced cell proliferation in acute myeloid leukaemia by enhancing tumour suppressors”, and that “Cdk8 is a colorectal cancer oncogene.” “Cdk8 activity is somehow enigmatic, since its functions vary considerably with the cell environment,” says Muñoz. “We have identified a number of Cdk8 targets that were unknown until now. This can help understand the function this protein regulates in other biological contexts.”

Going beyond genomics with proteomics

The study by the CNIO team shows the need for a greater focus on proteomics in cancer research strategies.

Research into and treatment of disease have made huge progress in the past decades, courtesy of the techniques used in molecular biology. Two of the most frequently used techniques are genomics, the analysis of the DNA sequence – the molecule that carries all our genetic information – and transcriptomics, the study of the sets of RNA transcripts – the molecules that translate into proteins. Proteins are macromolecules that are directly involved in chemical processes essential for life. The proteomic approach was adopted relatively recently by biomedical researchers. Proteomics has gained momentum over the past 15 years, yet it has become essential for genomics and transcriptomics to come full circle. Genomics and proteomics study processes that take place before proteins are produced. “We use proteomics to study a number of properties of proteins that cannot be analysed by studying DNA or RNA,” says Martínez del Val. This is extremely important, since “proteins are responsible for a whole range of basic life functions that take place within cells,” Muñoz adds.

The study was funded by the Spanish Ministry of Science and Innovation, the Ramón y Cajal Programme, and the Carlos III Health Institute. Researchers from the Institute for Research in Biomedicine (IRB), Barcelona, were also involved to take part in the study, which got support from the CNIO’s Experimental Therapeutics Programme.

Reference article

Dissection of two routes to naïve pluripotency using different kinase inhibitors. Ana Martínez-Val, Cian Lynch, Isabel Calvo, Pilar Ximénez-Embún, Fernando García, Eduardo Zarzuela, Manuel Serrano, Javier Muñoz (Nature Communications, 2021). DOI: 10.1038/s41467-021-22181-5

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