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How do single cells communicate in a tissue? How can these interactions be modeled, while retaining information of spatial context? Researchers around Fabian Theis from Helmholtz Munich Computational Health Center and Technical University of Munich (TUM) have generated a new method to represent cell communication: the node-centric expression models (NCEM). These models are based on graph neural networks and helps to uncover the effects of cell tissue niche composition on gene expression without loss of spatial information.
Cells interact in various different ways and on multiple length-scales. The interaction of a cell with its tissue niche can be described through cell communication events. To understand these events, researchers around the world create models, based on different strategies. The knowledge is crucial to understand and identify emerging phenomena in tissue microenvironments, such as genetic changes in a tumor. The issue: many of the models are based on dissociated cells, meaning that the cells are separated to individual cells when being analyzed and are no longer integrated in their natural environment. Other models are limited to receptor-ligand signaling, a certain type of communication between cells. These models therefore ignore the spatial proximity of a group of cells (a niche) in their natural tissue environment. Researchers around Fabian Theis from the Computational Health Center at Helmholtz Munich and Technical University of Munich (TUM) have now developed a new method, that defines the complexity and improves the understanding of cell communication: the node-centric expression models (NCEM).
A flexible framework
The particularity of the newly generated model: NCEM is a computational method based on graph neural networks, which combine transcriptomic variance attribution and cell communication modeling in a single model of tissue niches. The model is therefore able to predict a cell’s gene expression profile based on the presence of surrounding cell types. In addition, it estimates the effect of a tissue niche composition on gene expression in an unbiased manner from spatial molecular profiling data.
In their model, the researchers developed a flexible framework to explain gene expression variations observable in spatial transcriptomics, a technology providing spatially-resolved gene expression information. Gene expression variations can then be associated to known molecular processes associated with cell communication events. They showed that NCEMs robustly identify cell-cell dependencies across different spatial transcriptomics technologies and at length scales that are characteristic for known communication mechanisms. With this method, first authors David Fischer and Anna Schaar were thereby able to recover signatures of molecular processes, that are known to underlie cell communication.
A novel way to identify cell communication
The framework constraints communication events to cells that are proximal in space. The identified dependencies are not limited to ligand-receptor-based communication but can also explain, for example, physical interactions or metabolite exchange.
NCEM is a flexible computational method that can be extended to more complex data sets, as for example 3D spatial transcriptomics data and higher-throughput data. It therefore provides a flexible toolset for the analysis of cell-cell-communication in space. The novel methodology complements recent efforts on characterizing gene expression in individual cells in single-cell “atlas” projects by accounting in this particular case for the tissue niche.
About the scientists:
Prof Dr Dr Fabian Theis, Director of Helmholtz Munich, Computational Health Center; Professor of Mathematical Modelling of Biological Systems at the Technical University of Munich (TUM), TUM School of Life Sciences Weihenstephan, TUM School of Computation, Information and Technology.
Prof Dr Dr Fabian Theis, email@example.com
Fischer and Schaar et al. (2022). Modeling intercellular communication in tissues using spatial graphs of cells, Nature Biotechnology, 10.1038/s41587-022-01467-z
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