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Nova · Professor Researcher · re-ranking top 20…
Michael John Bennett

Michael John Bennett

Verified

University of Pennsylvania · Rehabilitation Medicine

Active 1972–2024

h-index58
Citations14.8k
Papers35620 last 5y
Funding$5.0M
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Research topics

  • Medicine
  • Chemistry
  • Internal medicine
  • Bioinformatics
  • Gastroenterology
  • Computational biology
  • Genetics
  • Obstetrics
  • Biochemistry
  • Mathematics
  • Biology

Selected publications

  • The Metabolomic Signature of the Placenta in Spontaneous Preterm Birth

    International Journal of Molecular Sciences · 2020 · 69 citations

    • Obstetrics
    • Medicine
    • Computational biology

    H-palmitate in SPTB placenta was lower than term. Collectively, significant and biologically relevant alterations in the placenta metabolome were identified in SPTB placenta. Altered acylcarnitine levels and fatty acid oxidation suggest that disruption in normal substrate metabolism is associated with SPTB.

  • Mitochondrial dysfunction in inflammatory bowel disease alters intestinal epithelial metabolism of hepatic acylcarnitines

    Journal of Clinical Investigation · 2020 · 91 citations

    • Medicine
    • Internal medicine
    • Gastroenterology

    As the interface between the gut microbiota and the mucosal immune system, there has been great interest in the maintenance of colonic epithelial integrity through mitochondrial oxidation of butyrate, a short-chain fatty acid produced by the gut microbiota. Herein, we showed that the intestinal epithelium could also oxidize long-chain fatty acids, and that luminally delivered acylcarnitines in bile could be consumed via apical absorption by the intestinal epithelium, resulting in mitochondrial oxidation. Finally, intestinal inflammation led to mitochondrial dysfunction in the apical domain of the surface epithelium that may reduce the consumption of fatty acids, contributing to higher concentrations of fecal acylcarnitines in murine Citrobacter rodentium-induced colitis and human inflammatory bowel disease. These results emphasized the importance of both the gut microbiota and the liver in the delivery of energy substrates for mitochondrial metabolism by the intestinal epithelium.

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