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Microbiota, which plays a vital role in susceptibility to Clostridioides difficile infection (CDI), synthesizes butyrate. Enteric glia is a component of the enteric nervous system (ENS) and is affected by C. difficile toxins A (TcdA) and B (TcdB). Here, we evaluated whether butyrate modulates the response of enteric glia to C. difficile toxins. In vitro, rat enteric glia were incubated with TcdA or TcdB alone, or in combination with butyrate 1 h before the toxin challenge. After 18 h incubation, enteric glia were collected to analyze cell death and expression of Bcl2 (an antiapoptotic factor), S100B, and IL-6 by qPCR. C. difficile toxins induced enteric glia death, increased levels of caspase 3/7, downregulated Bcl2, and upregulated the expression of pro-inflammatory mediators (S100B and IL-6). In high concentration, butyrate (200 µM) potentialized the effects of C. difficile toxins in promoting enteric glia death and caspase 3/7 activity. In contrast, a low butyrate concentration (0.2 µM) decreased enteric glia death and caspase 3/7 activity induced by C. difficile toxins. In addition, a low concentration of butyrate (0.2 µM) upregulated Bcl2 expression compared to control cells and decreased the downregulation of Bcl2 and upregulation of IL-6 induced by TcdB. Further, a low butyrate concentration (0.2 µM) also diminished S100B upregulation induced by TcdA. Our findings suggest that low and high concentrations of butyrate can differentially affect the susceptibility of enteric glia to C. difficile toxins. These findings bring new perspectives on how microbiota-derived products may modulate the response of enteric glia to C. difficile toxins.
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http://dx.doi.org/10.1002/jbt.70475 | DOI Listing |
Elife
September 2025
Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Sickness-induced sleep is a behavior conserved across species that promotes recovery from illness, yet the underlying mechanisms are poorly understood. Here, we show that interleukin-6-like cytokine signaling from the gut to brain glial cells regulates sleep. Under healthy conditions, this pathway promotes wakefulness.
View Article and Find Full Text PDFJ Biochem Mol Toxicol
September 2025
Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.
Microbiota, which plays a vital role in susceptibility to Clostridioides difficile infection (CDI), synthesizes butyrate. Enteric glia is a component of the enteric nervous system (ENS) and is affected by C. difficile toxins A (TcdA) and B (TcdB).
View Article and Find Full Text PDFNeuropharmacology
November 2025
International Translational Neuroscience Research Institute, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China. Electronic address:
We celebrate the life of our colleague Francesco Di Virgilio, who in his very last public lecture discussed purinergic signaling in neuroglia in physiology and pathophysiology. Here, we write on a subset of a unique type of peripheral neuroglia, enteric glia that accompany enteric neurons in the enteric nervous system of the gut and act to maintain homeostasis in enteric neurocircuits. Bi-directional communication between enteric neurons and glia is majorly mediated by purines.
View Article and Find Full Text PDFNeurogastroenterol Motil
August 2025
Department of Physiology, Michigan State University, East Lansing, Michigan, USA.
Background: The enteric nervous system (ENS) regulates essential gut functions through interactions between neurons and glial cells. While tools for studying neuronal activation are well-established, methods for tracking neuronal inactivation remain underdeveloped. Phosphorylated pyruvate dehydrogenase (pPDH) has emerged as a marker of neuronal inactivity in the brain.
View Article and Find Full Text PDFACS Nano
August 2025
National Engineering Research Center for Biomaterials, College of Biomedical Engineering, Med-X Center for Materials, Sichuan University, Chengdu 610064, China.
The gut's inflammation is governed by the enteric nervous system, where enteric glial cells (EGCs) serve as essential intermediaries between the nervous and immune systems. During inflammation, elevated levels of S100 calcium-binding protein B (S100B) from hyperactive EGCs initiate a proinflammatory cascade by inducing the excessive production of reactive oxygen species (ROS) and proinflammatory molecules, including S100B itself, thus establishing a detrimental feedback loop. Herein, we develop a S100B inhibitor pentamidine (PTM)-loaded olsalazine-based nanoneedle, Zn(Olsa)/PTM, to break this vicious cycle and alleviate ulcerative colitis.
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