Platelets and Defective N-Glycosylation

Int J Mol Sci. 2020 Aug 6;21(16):5630. doi: 10.3390/ijms21165630.


N-glycans are covalently linked to an asparagine residue in a simple acceptor sequence of proteins, called a sequon. This modification is important for protein folding, enhancing thermodynamic stability, and decreasing abnormal protein aggregation within the endoplasmic reticulum (ER), for the lifetime and for the subcellular localization of proteins besides other functions. Hypoglycosylation is the hallmark of a group of rare genetic diseases called congenital disorders of glycosylation (CDG). These diseases are due to defects in glycan synthesis, processing, and attachment to proteins and lipids, thereby modifying signaling functions and metabolic pathways. Defects in N-glycosylation and O-glycosylation constitute the largest CDG groups. Clotting and anticlotting factor defects as well as a tendency to thrombosis or bleeding have been described in CDG patients. However, N-glycosylation of platelet proteins has been poorly investigated in CDG. In this review, we highlight normal and deficient N-glycosylation of platelet-derived molecules and discuss the involvement of platelets in the congenital disorders of N-glycosylation.

Keywords: N-glycans; congenital disorders of N-glycosylation; hemostasis; megakaryopoiesis; platelets; thrombosis.

Publication types

  • Review

MeSH terms

  • Animals
  • Blood Platelets / metabolism*
  • Calcium / metabolism
  • Energy Metabolism
  • Glycosylation
  • Homeostasis
  • Humans
  • Models, Biological


  • Calcium