Camel whey protein protects lymphocytes from apoptosis via the PI3K-AKT, NF-κB, ATF-3, and HSP-70 signaling pathways in heat-stressed male mice

Biochem Cell Biol. 2018 Aug;96(4):407-416. doi: 10.1139/bcb-2017-0217. Epub 2017 Nov 22.

Abstract

Heat stress (HS) is an environmental factor that depresses the immune systems that mediate dysfunctional immune cells. Camel whey protein (CWP) can scavenge free radicals and enhance immunity. This study investigated the impact of dietary supplementation with CWP on immune dysfunction induced by exposure to HS. Male mice (n = 45) were distributed among 3 groups: control group; HS group; and HS mice that were orally administered CWP (HS + CWP group). The HS group exhibited elevated levels of reactive oxygen species (ROS) and pro-inflammatory cytokines (interleukin (IL)-1β, IL-6, tumor necrosis factor-α) as well as a significant reduction in the IL-2 and IL-4 levels. Exposure to HS resulted in impaired phosphorylation of AKT and IκB-α (nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha); increased expression of activating transcription factor 3 (ATF-3) and 70 kDa heat shock proteins (HSP70); and aberrant distribution of CD3+ T cells and CD20+ B cells in the thymus and spleen. Interestingly, HS mice treated with CWP presented significantly restored levels of reactive oxygen species and pro-inflammatory cytokines near the levels observed in the control mice. Furthermore, supplementation of HS mice with CWP enhanced the phosphorylation of AKT and IκB-α; attenuated the expression of ATF-3, HSP70, and HSP90; and improved T and B cell distributions in the thymus and spleen. Our findings reveal a potential immunomodulatory effect of CWP in attenuating immune dysfunction induced by exposure to thermal stress.

Keywords: antioxidants; antioxydants; camel whey protein; choc thermique; free radicals; heat stress; lymphocytes; protéine du lactosérum du chameau; radicaux libre.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activating Transcription Factor 3
  • Animals
  • Apoptosis / drug effects*
  • Dietary Supplements
  • HSP70 Heat-Shock Proteins / metabolism
  • Lymphocytes / drug effects*
  • Male
  • Mice, Inbred C57BL
  • NF-kappa B / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Protective Agents / pharmacology
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / drug effects*
  • Whey Proteins / pharmacology*

Substances

  • Activating Transcription Factor 3
  • Atf3 protein, mouse
  • HSP70 Heat-Shock Proteins
  • NF-kappa B
  • Protective Agents
  • Whey Proteins
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt