Cellular competition is a crucial quality control process that ensures that the development of an organism relies on healthy cells. Researchers revealed the secrets underlying cell competition and what features can pre-determine whether a cell will survive or not. Defects in energy production are critical in making cells vulnerable to elimination. The study was led by researchers from Helmholtz Zentrum München and Imperial College London.

As multicellular life relies on cell-cell interactions, it is not surprising that this is not always peaceful: Cells with higher fitness eliminate cells with lower fitness through cell competition. Cell competition has emerged as a quality control mechanism and occurs when cells differ, genetically or otherwise, from each other. In mammals, the process of cell competition has been observed, e.g., in cancer, during organ homeostasis, and during development as a process to select the fittest cells in the embryo and the adult. However, the features that distinguish “winner” from “loser” cells and whether there are key determinants for cell competition in various biological contexts remain elusive.

The recipe for elimination of “loser” cells

The research team found out that the cells losing the competition are characterized by defective mitochondria and, in mouse embryos, they are marked by sequence changes in their mitochondrial genome. Their work was published in the journal Nature Metabolism. “Our work suggests that differences in mitochondrial activity are key determinants of competitive cell fitness in a wide range of systems. In particular, we discovered that genetic defects in the mitochondria characterize ‘loser’ cells in mouse embryos,” says Antonio Scialdone, co-corresponding author of the article.

The mouse embryo uses cellular competition to get rid of unfit epiblast cells before the basic body plan is laid down during gastrulation. Using single-cell RNAseq (a specific sequencing technique), the researchers compared cells in embryos treated with a cell death inhibitor versus those in untreated mouse embryos. By applying machine learning algorithms, they could identify the gene expression signature of “loser” cells and discovered that these cells have defective mitochondria and are marked by sequence changes in their mitochondrial genome. “It was nice to see how with our computational pipeline we were able to extract such important information from the single-cell RNAseq datasets,” says Gabriele Lubatti co-first author of the article.

The information on how “loser” cells look in the mouse embryo allowed them to determine a “loser” cell identity. By analyzing the mitochondrial activity in other cell competition models, they could identify that mitochondrial dysfunction is a common characteristic in different “loser” cells and that small changes in the mitochondrial DNA are enough to drive cell competition.

Future work

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