Differential sialic acid content in adult and neonatal fibrinogen mediates differences in clot polymerization dynamics

• Published in: Blood advances 2021-12, Vol.5 (23), p.5202-5214
• Main Authors: Nellenbach, Kimberly, Kyu, Alexander, Guzzetta, Nina, Brown, Ashley C.
• Format: Article
• Language: English
• Subjects: Adult; Fibrin; Fibrinogen; Fibrinopeptide A; Humans; Infant, Newborn; N-Acetylneuraminic Acid; Polymerization; Thrombosis and Hemostasis
• ISSN: 2473-9529; 2473-9537
• DOI: 10.1182/bloodadvances.2021004417

Neonates possess a molecular variant of fibrinogen, known as fetal fibrinogen, characterized by increased sialic acid, a greater negative charge, and decreased activity compared with adults. Despite these differences, adult fibrinogen is used for the treatment of bleeding in neonates, with mixed efficacy. To determine safe and efficacious bleeding protocols for neonates, more information on neonatal fibrin clot formation and the influence of sialic acid on these processes is needed. Here, we examine the influence of sialic acid on neonatal fibrin polymerization. We hypothesized that the increased sialic acid content of neonatal fibrinogen promotes fibrin B:b knob-hole interactions and consequently influences the structure and function of the neonatal fibrin matrix. We explored this hypothesis through analysis of structural properties and knob:hole polymerization dynamics of normal and desialylated neonatal fibrin networks and compared them with those formed with adult fibrinogen. We then characterized normal neonatal fibrin knob:hole interactions by forming neonatal and adult clots with either thrombin or snake-venom thrombin-like enzymes that preferentially cleave fibrinopeptide A or B. Sialic acid content of neonatal fibrinogen was determined to be a key determinant of resulting clot properties. Experiments analyzing knob:hole dynamics indicated that typical neonatal fibrin clots are formed with the release of more fibrinopeptide B and less fibrinopeptide A than adults. After the removal of sialic acid, fibrinopeptide release was roughly equivalent between adults and neonates, indicating the influence of sialic acid on fibrin neonatal fibrin polymerization mechanisms. These results could inform future studies developing neonatal-specific treatments of bleeding. •Increased sialic acid in neonatal fibrinogen influences fibrin knob-hole interactions during polymerization.•Neonatal fibrin polymerization involves more B knob– and fewer A knob–mediated interactions compared with adults. [Display omitted]