DNase I improves blood-milk barrier integrity and alleviates inflammation induced by Staphylococcus aureus during mastitis

Int Immunopharmacol. 2021 Nov:100:108079. doi: 10.1016/j.intimp.2021.108079. Epub 2021 Aug 27.

Abstract

Mastitis is an inflammation of mammary gland, which directly affects the milk production performance and causes huge economic losses in the dairy industry. During mastitis, the blood-milk barrier (BMB) loses its integrity and aggravates the severity of mastitis. Exogenous DNase I has been exerted protective effects in different model of tissue injury. Here, we designed a study to investigate the effects of DNase I on inflammation and BMB in a mice model of Staphylococcus aureus-induced mastitis. In the model, we found that DNase I treatment significantly alleviated the inflammatory response through decrease of inflammatory cells in mammary alveoli, MPO activity and cytokines in mammary gland. Furthermore, immunofluorescent staining and western blotting demonstrated that exogenous DNase I obviously reduced BMB permeability and changed the expression of tight junction proteins to support the re-establishment of the barrier integrity. Mechanismly, DNase I treatment inhibited NF-κB and enhanced AKT signaling pathways. Therefore, our results indicate that DNase I may be an effective treatment for attenuating mastitis.

Keywords: Blood-milk barrier; DNase I; Mastitis; Staphylococcus aureus.

MeSH terms

  • Animals
  • Deoxyribonuclease I / pharmacology*
  • Deoxyribonuclease I / therapeutic use
  • Female
  • Humans
  • Lipopolysaccharides / administration & dosage
  • Lipopolysaccharides / immunology
  • Mammary Glands, Animal / blood supply
  • Mammary Glands, Animal / immunology
  • Mammary Glands, Animal / microbiology
  • Mammary Glands, Animal / pathology
  • Mastitis / drug therapy*
  • Mastitis / immunology
  • Mastitis / microbiology
  • Mastitis / pathology
  • Mice
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • Staphylococcal Infections / drug therapy*
  • Staphylococcal Infections / immunology
  • Staphylococcal Infections / pathology
  • Staphylococcus aureus / immunology

Substances

  • Lipopolysaccharides
  • Deoxyribonuclease I