Effect of peptidoglycans on erythrocyte survival

Michael Föller1, Raja Biswas, Hasan Mahmud

  • 1Department of Physiology, University of Tübingen, Tübingen, Germany.

Insights

Bacterial peptidoglycans (PGNs) trigger suicidal erythrocyte death (eryptosis) by increasing intracellular calcium. This process contributes to anemia during bacterial infections.

Area of Science:

  • Immunology
  • Hematology
  • Cell Biology

Background:

  • Peptidoglycans (PGNs) are pathogen-associated molecular patterns (PAMPs) from bacterial cell walls.
  • Bacterial infections can cause anemia, potentially due to accelerated erythrocyte death.

Purpose of the Study:

  • To investigate the effect of PGNs on eryptosis, a form of programmed suicidal death in erythrocytes.
  • To elucidate the mechanisms by which PGNs induce eryptosis.

Main Methods:

  • Erythrocyte exposure to PGNs.
  • Measurement of cytosolic Ca(2+) concentration using Fluo3 fluorescence.
  • Assessment of ceramide formation, phosphatidylserine exposure (annexin V-binding), and erythrocyte volume (FACS).
  • Evaluation of intracellular ATP concentration and effect of extracellular Ca(2+).

Main Results:

  • PGNs increased cytosolic Ca(2+) concentration and ceramide formation in erythrocytes.
  • PGNs enhanced phosphatidylserine exposure and decreased erythrocyte volume.
  • Intracellular ATP concentration decreased, and the effect was dependent on extracellular Ca(2+).
  • In vivo clearance of PGN-exposed erythrocytes was significantly enhanced.

Conclusions:

  • Peptidoglycans induce eryptosis in erythrocytes, partly via increased cytosolic Ca(2+) concentration.
  • PGN-induced eryptosis may contribute to anemia development during bacterial infections.

Related Concept Videos

Inhibitors of Gram-positive Cell Wall Synthesis01:23

Inhibitors of Gram-positive Cell Wall Synthesis

Bacterial cell walls are typically rigid structures composed mainly of peptidoglycan, a mesh-like polymer that provides mechanical strength and maintains cell shape. The synthesis of peptidoglycan is a crucial process in bacterial growth and serves as a primary target for many antibiotics.Mechanism of Action of Beta-Lactam AntibioticsBeta-lactam antibiotics, such as penicillin, inhibit peptidoglycan synthesis in actively growing cells. These antibiotics share a characteristic four-membered...
Stringent Response in E. coli01:23

Stringent Response in E. coli

Bacterial growth is closely tied to nutrient availability, with cells proliferating exponentially under favorable conditions and entering a stationary phase when resources become scarce. This transition is mediated by a regulatory mechanism known as the stringent response, which allows bacteria to adapt to nutrient deprivation by modulating gene expression and metabolic activity.During nutrient scarcity, intracellular amino acid levels decline. It results in the accumulation of uncharged tRNAs...
Protein Folding Quality Check in the RER01:29

Protein Folding Quality Check in the RER

ER is the primary site for the maturation and folding of soluble and transmembrane secretory proteins. The calnexin cycle is a specific chaperone system that folds and assesses the confirmation of N-glycosylated proteins before they can exit the ER lumen. The primary players of this quality check pipeline are the lectins, ER-resident chaperones, and a glucosyl transferase enzyme. In case the calnexin system in the lumen fails to salvage a misfolded protein, it is transported to the cytoplasm...
Peptidoglycan Synthesis01:28

Peptidoglycan Synthesis

Structure of PeptidoglycanPeptidoglycan is a vital structural component of the bacterial cell wall, providing mechanical strength and shape to the cell. It consists of repeating units of two sugars—N-acetylglucosamine (NAG) and N-acetylmuramic acid (NAM)—linked by β-1,4 glycosidic bonds. These sugar chains are cross-linked by short peptide chains, forming a mesh-like polymer that surrounds the bacterial plasma membrane.Cytoplasmic Phase – Precursor SynthesisPeptidoglycan biosynthesis begins in...
Proteoglycans01:05

Proteoglycans

Glycans, a class of complex heterogeneous molecules, can be covalently attached to proteins to form glycosylated proteins that regulate various physiological and pathological processes. Glycosylated proteins or glycoproteins comprise N-linked and O-linked oligosaccharides. O-glycosylation is the most common type of protein glycosylation. Here, glycans attach to the oxygen atom of the hydroxyl groups of Serine or Threonine residues. O-linked glycosylation occurs later in protein processing,...