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Biology subjects

Leader, A.

Publications and source records attributed to Leader, A..

3 recordsLinked to original sources

Biochemical network motifs can transduce and process oscillatory information

Biological networks that are formed through amalgamation of signaling pathways include recurrent configurations called network motifs. These statistically over-represented subgraphs are often formed through interconnected enzyme-substrate relationships that are known to result in highly dynamic downstream behavior, including oscillatory output. Such signals are abundant in biology: heartbeats, circadian rhythms, and cell cycles all exhibit characteristic frequencies. Though there has been great emphasis on how oscillations can be generated through network dynamics, little is known about oscillatory information processing or transduction capacity of network motifs. We employ ordinary differential equations-based dynamical modeling to understand how different network topologies impact oscillatory signal propagation through a multi-enzyme network. We model enzyme-substrate interactions of 20 commonly observed motifs using Michaelis-Menten kinetics. We then perform deterministic Monte Carlo simulations using a range of biologically relevant enzymatic parameters and input frequencies. From these simulations, we quantify signal propagation characteristics using cluster analysis, categorize different motif responses based on output characteristics, and identify potential mechanisms for oscillatory signal processing using parameter sensitivity analysis. We see that the input-output responses depend on network topology and enzyme kinetic parameters. Enzymatic motifs show median oscillatory suppression of 30-135 decibels, with three-node coherent feedforward loops showing the lowest propensity for oscillatory signal suppression. Motifs that contained negative feedback or four-node coherent feedforward loops had the biggest potential to act as AC-to-DC converters, translating oscillatory input signals into transient impulses or sustained continuous outputs, respectively. We conclude that enzyme networks can process and decode information within oscillatory inputs in a frequency- and network-dependent manner.

systems biology↗

Disruption of the CSF-1-CSF-1R axis alters cerebellar microglia and is associated with motor and social interaction defects

Microglia, the brain resident macrophages, critically shape forebrain neuronal circuits. However, their precise function in the cerebellum is unknown. Here we show that human and mouse cerebellar microglia express a unique molecular program distinct from forebrain microglia. Cerebellar microglial identity was driven by the CSF-1R ligand CSF-1, independently of the alternate CSF-1R ligand, IL-34. Accordingly, CSF-1 depletion from Nestin+ cells led to severe depletion and transcriptional alterations of cerebellar microglia, while microglia in the forebrain remained intact. Strikingly, CSF-1 deficiency and alteration of cerebellar microglia were associated with reduced Purkinje cells, altered neuronal function, and defects in motor learning and social novelty interactions. These findings reveal a novel CSF-1-CSF-1R signaling-mediated mechanism that contributes to motor function and social behavior.\n\nSummaryMicroglia are a heterogeneous population whose identity and function are dictated by signals from their microenvironment. Kana et al. show that CSF-1 signaling is critical for maintaining cerebellar microglial transcriptional identity and homeostasis, and that altering the CSF-1 - CSF-1R axis leads to motor and behavioral defects.

neuroscience↗

Single-cell analysis of Crohn’s disease lesions identifies a pathogenic cellular module associated with resistance to anti-TNF therapy

Clinical benefits to cytokine blockade in ileal Crohns disease (iCD) have been limited to a subset of patients. Whether cellular and molecular heterogeneity contributes to variability in treatment responses has been unclear. Using single cell technologies combining scRNAseq, CyTOF and multiplex tissue imaging, we mapped the cellular landscape of inflamed ileum lesions, adjacent non-inflamed ileum and matched circulating blood cells of iCD patients. In inflamed tissues, we identified a pathogenic module characterized by an inflammatory mononuclear phagocyte (Inf.MNP)-associated cellular response organized around inflammatory macrophages and mature dendritic cells in a subset of iCD patients. We confirmed the Inf.MNP-associated cellular response in 4 independent iCD cohorts (n=441) and showed that presence of this pathogenic module at diagnosis correlated with primary resistance to anti-TNF therapy. Single cell mapping of iCD tissues identifies a complex cellular signature of anti-TNF resistance thereby revealing novel biomarkers of treatment response and tailored therapeutic opportunities.

immunology↗