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Related Concept Videos

Mucosal Barrier of the Stomach01:25

Mucosal Barrier of the Stomach

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The gastric glands contain parietal cells that secrete hydrochloric acid (HCl) for digestion. The cells secrete HCl because it is highly corrosive and essential for breaking down food. To achieve this, they secrete hydrogen and chloride ions into the lumen of the gastric glands, which combine to form HCl.
Within parietal cells, carbonic acid is first formed through the reaction of water and carbon dioxide. The dissociation of carbonic acid releases bicarbonate and hydrogen ions. The bicarbonate...
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Role Of Notch Signalling In Intestinal Stem Cell Renewal01:12

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Notch signaling was first discovered in Drosophila melanogaster, where it is involved in cell lineage differentiation. Notch signaling regulates the maintenance and differentiation of intestinal stem cells or ISCs by controlling the expression of atonal homolog 1 or Atoh1. Atoh1 directs cells to differentiate into secretory cells.
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Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
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Intestinal Phase of Digestion01:29

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The intestinal phase of digestion is the third and final stage of the digestive process, occurring after the cephalic and gastric phases. It begins when chyme, a partially digested mixture of food and digestive enzymes, enters the small intestine from the stomach. This phase is crucial for nutrient absorption and involves complex hormonal and enzymatic interactions.
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Gastritis-II: Pathophysiology01:17

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Gastritis is marked by disruption of the mucosal barrier that usually protects the stomach tissue from digestive juices and manifests in acute and chronic forms.
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Renewal of Intestinal Stem Cells01:23

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The intestinal epithelial lining rapidly renews every 4 to 5 days. The renewal is facilitated by intestinal stem cells (ISCs) located at the base of the crypt– a gland located at the bottom of each villus. ISCs divide asymmetrically to form new stem cells and progenitor daughter cells. The daughter cells are called transit-amplifying (TA) cells which move upwards along the crypt and either differentiate into absorptive cells– the enterocytes or secretory cells– including the...
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Related Experiment Video

Updated: May 17, 2025

Assessment of Gut Barrier Integrity in Mice Using Fluorescein-Isothiocyanate-Labeled Dextran
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cGAS-STING Pathway's Impact on Intestinal Barrier.

Liqi Li1, Yingge He2, Yu Chen3

  • 1Department of General Surgery, Xinqiao Hospital, Army Medical University, Chongqing, China.

Journal of Gastroenterology and Hepatology
|May 16, 2025
PubMed
Summary

The cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway is implicated in intestinal inflammation and barrier dysfunction. Understanding its role is crucial for addressing metabolic dysregulation in compromised gut health.

Keywords:
cGAS‐STINGinflammatory bowel diseaseintestinal barrier functionintestinal ischemia/reperfusion injury

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Investigating Intestinal Barrier Breakdown in Living Organoids
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Area of Science:

  • Immunology
  • Gastroenterology
  • Molecular Biology

Background:

  • Intestinal inflammation and barrier dysfunction are linked to metabolic issues.
  • The cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway is a key signaling pathway involved in innate immunity.
  • This pathway responds to cytosolic double-stranded DNA (dsDNA).

Purpose of the Study:

  • To review the role and impact of the cGAS-STING pathway on intestinal barrier function.
  • To explore the molecular mechanisms of cGAS-STING signaling in the gut.
  • To understand how cGAS-STING activation affects intestinal epithelial cells and immune responses.

Main Methods:

  • Literature review of studies on the cGAS-STING pathway in intestinal inflammation.
  • Analysis of molecular mechanisms involving cGAS, STING, TBK1, IRF3, and NF-κB.
  • Examination of the pathway's effects on intestinal epithelial cells (IECs) and immune cells.

Main Results:

  • cGAS activation by dsDNA produces cyclic GMP-AMP (cGAMP).
  • cGAMP binding to STING initiates signaling cascades involving TBK1, IRF3, and NF-κB.
  • This activation leads to the production of type I interferon and proinflammatory cytokines.
  • The pathway's effects differ across various intestinal cell types.

Conclusions:

  • The cGAS-STING pathway significantly influences intestinal barrier integrity and inflammation.
  • Dysregulation of this pathway may contribute to metabolic disturbances associated with compromised gut barrier function.
  • Further research into the cGAS-STING pathway could reveal therapeutic targets for intestinal diseases.