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Biology subjects

Krawczyk, J.

Publications and source records attributed to Krawczyk, J..

2 recordsLinked to original sources

Cellohood: multi-granular discovery of cellular neighborhoods with a permutation-invariant set transformer auto-encoder

Discovering cellular neighborhoods and their roles in disease requires computational methods that consider the full breadth of data and offer multi-level granularity and interpretability. Here, we introduce Cellohood, a permutation-invariant set transformer auto-encoder equipped with a clinical association pipeline. Cellohood encodes full readouts for bags of spatially co-localized cells and supports multi-level analyses, providing interpretability by mapping latent dimensions to spatial tissue features. Our model surpasses current methods in accuracy of cellular neighborhood detection for spatial transcriptomics of the human cortex and CODEX spleen data measuring lupus progression. Applied to cancer data across three granularity levels, our method recovers neighborhoods along the expected immune-cold to immune-hot spectrum and further refines them into biologically and clinically meaningful subclasses, revealing spatial patterns linked to prognosis, histology, stage, and tumor mutational burden, and uncovering subgroups that transcend standard classifications. Overall, Cellohood enables in-depth analysis of complex tissues, revealing clinically informative spatial neighborhoods.

bioinformatics↗

The Diabetes Gene Tcf7l2 Organizes Gene Expression in the Liver and Regulates Amino Acid Metabolism

TCF7L2 harbors the strongest genetic association with diabetes identified thus far. However, its function in liver has remained unclear. Here, we find using mice with liver-specific deletion, that Tcf7l2 plays a central role in maintaining hepatic zonation. That is, in the normal liver, many genes show gradients of expression across the liver lobule; in the absence of Tcf7l2, these gradients collapse. One major consequence is the disorganization of glutamine metabolism, with a loss of the glutamine production program, ectopic expression of the glutamine consumption program, and a decrease in glutamine levels. In parallel, metabolomic profiling shows glutamine to be the most significantly decreased metabolite in individuals harboring the rs7903146 variant in TCF7L2. Taken together, these data indicate that hepatic TCF7L2 has a secondary role in glycemic control, but a primary role in maintaining transcriptional architecture and glutamine homeostasis.

physiology↗