Carnosine induces intestinal cells to secrete exosomes that activate neuronal cells.
Yuka SugiharaShiori OnoueKosuke TashiroMikako SatoTakanori HasegawaYoshinori KatakuraPublished in: PloS one (2019)
Recently, we showed that imidazole dipeptide such as carnosine contained abundantly in chicken breast meat improves brain function in a double-blind randomized controlled trial. However, the underlying molecular mechanisms remain unknown. Here, we investigated whether carnosine activates intestinal epithelial cells and induces the secretion of factors that activate brain function. We focused on exosomes derived from intestinal epithelial cells as mediators of brain-gut interaction. Results showed that exosomes derived from Caco-2 cells treated with carnosine significantly induced neurite growth in SH-SY5Y cells. To clarify the molecular basis of this finding, we performed integrated analysis of microRNAs (miRNAs) with altered expression in exosomes in response to carnosine treatment and mRNAs with altered expression in target cells in response to exosome treatment to identify related miRNAs and their target genes. The combination of miR-6769-5p and its target gene ATXN1 was found to be involved in the exosome-induced activation of neuronal cells.
Keyphrases
- induced apoptosis
- cell cycle arrest
- randomized controlled trial
- stem cells
- mesenchymal stem cells
- signaling pathway
- endoplasmic reticulum stress
- poor prognosis
- gene expression
- oxidative stress
- genome wide
- white matter
- systematic review
- multiple sclerosis
- transcription factor
- combination therapy
- brain injury
- cerebral ischemia
- high resolution
- blood brain barrier
- subarachnoid hemorrhage
- atomic force microscopy
- binding protein
- newly diagnosed
- single molecule
- stress induced