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Liebig's law of the minimum in the TGF-β/SMAD pathway. | LitMetric

AI Article Synopsis

  • Cells utilize signaling pathways like the TGF-β pathway to react to their environments in unique ways based on the abundance of signaling molecules.
  • The research combined modeling and experiments to show that the output of the TGF-β pathway is influenced by the least abundant signaling receptor, which shapes cellular responses in different types of cells, including cancer cell lines.
  • The study found that the receptor with lower abundance (either TGFBR1 or TGFBR2) determines signaling responses and highlights a principle that may apply to the variability in responses in other signaling pathways as well.

Article Abstract

Cells use signaling pathways to sense and respond to their environments. The transforming growth factor-β (TGF-β) pathway produces context-specific responses. Here, we combined modeling and experimental analysis to study the dependence of the output of the TGF-β pathway on the abundance of signaling molecules in the pathway. We showed that the TGF-β pathway processes the variation of TGF-β receptor abundance using Liebig's law of the minimum, meaning that the output-modifying factor is the signaling protein that is most limited, to determine signaling responses across cell types and in single cells. We found that the abundance of either the type I (TGFBR1) or type II (TGFBR2) TGF-β receptor determined the responses of cancer cell lines, such that the receptor with relatively low abundance dictates the response. Furthermore, nuclear SMAD2 signaling correlated with the abundance of TGF-β receptor in single cells depending on the relative expression levels of TGFBR1 and TGFBR2. A similar control principle could govern the heterogeneity of signaling responses in other signaling pathways.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11135686PMC
http://dx.doi.org/10.1371/journal.pcbi.1012072DOI Listing

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