4.5 Article

Small Bowel Resection Increases Paracellular Gut Barrier Permeability via Alterations of Tight Junction Complexes Mediated by Intestinal TLR4

期刊

JOURNAL OF SURGICAL RESEARCH
卷 258, 期 -, 页码 73-81

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jss.2020.08.049

关键词

Short gut; TLR4; Gut permeability; Tight junction; Intestinal resection; Mice; Intestinal barrier

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资金

  1. NIH [5T32DK077653, 5T32HD043010, T32DK007120, 5R01AI136515, 5R01DK119147]
  2. Children's Surgical Sciences Research Institute of the St. Louis Children's Hospital Foundation
  3. Children's Hope Foundation

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The study revealed increased intestinal permeability after small bowel resection in mice, but this alteration was mitigated by the knockout of intestinal-specific TLR4 gene.
Background: Short bowel syndrome resulting from small bowel resection (SBR) is associated with significant morbidity and mortality. Many adverse sequelae including steatohepatitis and bacterial overgrowth are thought to be related to increased bacterial translocation, suggesting alterations in gut permeability. We hypothesized that after intestinal resection, the intestinal barrier is altered via toll-like receptor 4 (TLR4) signaling at the intestinal level. Methods: B6 and intestinal-specific TLR4 knockout (iTLR4 KO) mice underwent 50% SBR or sham operation. Transcellular permeability was evaluated by measuring goblet cell associated antigen passages via two-photon microscopy. Fluorimetry and electron microscopy evaluation of tight junctions (TJ) were used to assess paracellular permeability. In parallel experiments, single-cell RNA sequencing measured expression of intestinal integral TJ proteins. Western blot and immunohistochemistry confirmed the results of the single-cell RNA sequencing. Results: There were similar number of goblet cell associated antigen passages after both SBR and sham operation (4.5 versus 5.0, P > 0.05). Fluorescein isothiocyanate-dextran uptake into the serum after massive SBR was significantly increased compared with sham mice (2.13 +/- 0.39 ng/mu L versus 1.62 +/- 0.23 ng/mu L, P < 0.001). SBR mice demonstrated obscured TJ complexes on electron microscopy. Single-cell RNA sequencing revealed a decrease in TJ protein occludin (21%) after SBR (P < 0.05), confirmed with immunostaining and western blot analysis. The KO of iTLR4 mitigated the alterations in permeability after SBR. Conclusions: Permeability after SBR is increased via changes at the paracellular level. However, these alterations were prevented in iTLR4 mice. These findings suggest potentialprotein targets for restoring the intestinal barrier and obviating the adverse sequelae of short bowel syndrome. (C) 2020 Elsevier Inc. All rights reserved.

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