Anti-Atherogenic Actions of the Lab4b Consortium of Probiotics In Vitro

Victoria L O'Morain1, Jing Chen1, Sue F Plummer2

  • 1Cardiff School of Biosciences, Cardiff University, Sir Martin Evans Building, Museum Avenue, Cardiff CF10 3AX, UK.

Insights

The Lab4b probiotic blend shows promise in combating atherosclerosis by reducing inflammation in blood vessels. This study reveals its anti-atherogenic effects on key cellular processes, suggesting potential therapeutic applications.

Area of Science:

  • Microbiology
  • Immunology
  • Cardiovascular Science

Background:

  • Probiotic bacteria offer protective effects against inflammatory disorders, but their mechanisms remain unclear.
  • The Lab4b probiotic consortium comprises four strains of lactic acid bacteria and bifidobacteria found in infants.
  • Atherosclerosis, a vascular inflammatory disease, has not been studied in relation to Lab4b probiotics.

Purpose of the Study:

  • To investigate the effects of the Lab4b probiotic consortium on cellular processes relevant to atherosclerosis.
  • To determine the anti-atherogenic potential of Lab4b in vitro using human monocytes/macrophages and vascular smooth muscle cells.

Main Methods:

  • Utilized Lab4b conditioned medium (CM) to treat human monocytes/macrophages and vascular smooth muscle cells in vitro.
  • Assessed the impact of Lab4b CM on monocyte migration, proliferation, LDL uptake, macropinocytosis, and foam cell formation.
  • Analyzed gene expression related to modified LDL uptake and cholesterol efflux in macrophages.

Main Results:

  • Lab4b CM attenuated monocyte migration, proliferation, modified LDL uptake, and macropinocytosis.
  • Lab4b CM induced phagocytosis and cholesterol efflux in macrophages, reducing foam cell formation.
  • Gene expression analysis showed decreased uptake of modified LDL and increased cholesterol efflux pathways.

Conclusions:

  • The Lab4b probiotic consortium exhibits significant anti-atherogenic properties in vitro.
  • Lab4b influences key cellular mechanisms involved in atherosclerosis development and progression.
  • Further in vivo studies in mouse models and clinical trials are warranted to confirm these findings.