Parenteral nutrition impairs lymphotoxin β receptor signaling via NF-κB

Ann Surg. 2011 May;253(5):996-1003. doi: 10.1097/SLA.0b013e31821224eb.

Abstract

Objective: To determine effects of (1) parenteral nutrition (PN), (2) exogenous Lymphotoxin β receptor (LTβR) stimulation in PN animals, and (3) exogenous LTβR blockade in chow animals on NF-κB activation pathways and products: MAdCAM-1, chemokine (C-C motif) Ligand (CCL) 19, CCL20, CCL25, interleukin (IL)-4, and IL-10.

Background: LT stimulates LTβR in Peyer's patches (PP) to activate NF-κB via the noncanonical pathway. The p100/RelB precursor yields p52/RelB producing MAdCAM-1, cytokines, and chemokines important in cell trafficking. TNFα, IL-1β, and bacterial products stimulate the inflammatory canonical NF-κB pathway producing p65/p50 and c-Rel/p50. PN decreases LTβR, MAdCAM-1, and chemokines in PP and lowers small intestinal IgA compared with chow.

Methods: Canonical (p50 and p65) and noncanonical (p52 and Rel B) NF-κB proteins in PP were analyzed by TransAM NF-κB kit after 5 days of chow or PN, 2 days of LTβR stimulation or 3 days of LTβR blockade. MAdCAM-1, chemokines, and cytokines in PP were measured by ELISA after LTβR stimulation or blockade.

Results: PN significantly reduced all NF-κB proteins in PP compared with chow. Exogenous LTβR stimulation during PN increased p50, p52, Rel B, MAdCAM-1, IL-4, and IL-10 in PP, but not p65, CCL19, CCL20, or CCL25 compared with PN. LTβR blockade reduced noncanonical products (p52 and Rel B), MAdCAM-1, CCL19, CCL20, CCL25, IL-4, and IL-10 but had no effect on the inflammatory pathway (p50 and p65) compared with chow.

Conclusion: Lack of enteral stimulation during PN decreases both canonical and noncanonical NF-κB pathways in PP. LTβR stimulation during PN feeding completely restores PP noncanonical NF-κB activity, MAdCAM-1, IL-4, IL-10, and partly the canonical pathway. LTβR blockade decreases the noncanonical NF-κB activity, MAdCAM-1, chemokines, and cytokines without effect on the canonical NF-κB activity in PP.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Analysis of Variance
  • Animals
  • Cell Adhesion Molecules
  • Chemokines / metabolism
  • Cytokines / metabolism
  • Disease Models, Animal
  • Immunoglobulins / metabolism
  • Interleukin-10 / metabolism
  • Interleukin-4 / metabolism
  • Intestinal Mucosa / metabolism
  • Lymphotoxin beta Receptor / metabolism*
  • Lymphotoxin beta Receptor / physiology
  • Male
  • Mice
  • Mice, Inbred Strains
  • Mucoproteins / metabolism
  • NF-kappa B / metabolism*
  • Parenteral Nutrition / adverse effects*
  • Parenteral Nutrition / methods
  • Random Allocation
  • Sensitivity and Specificity
  • Signal Transduction*

Substances

  • Cell Adhesion Molecules
  • Chemokines
  • Cytokines
  • Immunoglobulins
  • Lymphotoxin beta Receptor
  • MADCAM1 protein, human
  • Mucoproteins
  • NF-kappa B
  • Interleukin-10
  • Interleukin-4