Bryostatin-1 ameliorated experimental colitis in Il-10-/- Mice by protecting the intestinal barrier and limiting immune dysfunction

J Cell Mol Med. 2019 Aug;23(8):5588-5599. doi: 10.1111/jcmm.14457. Epub 2019 Jun 28.

Abstract

Bryostatin-1 (Bry-1) has been proven to be effective and safe in clinical trials of a variety of immune-related diseases. However, little is known about its effect on Crohn's disease (CD). We aimed to investigate the impact of Bry-1 on CD-like colitis and determine the mechanism underlying this effect. In the present study, 15-week-old male Il-10-/- mice with spontaneous colitis were divided into positive control and Bry-1-treated (Bry-1, 30 μg/kg every other day, injected intraperitoneally for 4 weeks) groups. Age-matched, male wild-type (WT) mice were used as a negative control. The effects of Bry-1 on colitis, intestinal barrier function and T cell responses as well as the potential regulatory mechanisms were evaluated. We found that the systemic delivery of Bry-1 significantly ameliorated colitis in Il-10-/- mice, as demonstrated by decreases in the disease activity index (DAI), inflammatory score and proinflammatory mediator levels. The protective effects of Bry-1 on CD-like colitis included the maintenance of intestinal barrier integrity and the helper T cell (Th)/regulatory T cell (Treg) balance. These effects of Bry-1 may act in part through nuclear factor erythroid 2-related factor 2 (Nrf2) signalling activation and STAT3/4 signalling inhibition. The protective effect of Bry-1 on CD-like colitis suggests Bry-1 has therapeutic potential in human CD, particularly given the established clinical safety of Bry-1.

Keywords: Crohn's disease; bryostatin-1; intestinal mucosal immunity; intestinal barrier.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Bryostatins / pharmacology
  • Bryostatins / therapeutic use*
  • Colitis / drug therapy*
  • Colitis / immunology*
  • Colitis / pathology
  • Down-Regulation / drug effects
  • Epithelial Cells / metabolism
  • Interleukin-10 / deficiency*
  • Interleukin-10 / metabolism
  • Intestines / immunology*
  • Intestines / pathology*
  • Mice, Inbred C57BL
  • NF-E2-Related Factor 2 / metabolism
  • Permeability
  • Signal Transduction / drug effects
  • T-Lymphocytes, Regulatory / drug effects
  • T-Lymphocytes, Regulatory / immunology
  • Th1 Cells / drug effects
  • Th1 Cells / immunology
  • Th17 Cells / drug effects
  • Th17 Cells / immunology
  • Tight Junction Proteins / metabolism
  • Tight Junctions / drug effects
  • Tight Junctions / metabolism
  • Tight Junctions / ultrastructure

Substances

  • Bryostatins
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, mouse
  • Tight Junction Proteins
  • Interleukin-10
  • bryostatin 1