Newly Identified HNP-F from Human Neutrophil Peptide-1 Promotes Hemostasis

Biotechnol J. 2019 Jul;14(7):e1800606. doi: 10.1002/biot.201800606. Epub 2019 May 2.

Abstract

Active hemostatic agents can play a crucial role in saving patients' lives during surgery. Active hemostats have several advantages including utilization of natural blood coagulation and biocompatibility. Among them, although human neutrophil peptide-1 (HNP-1) has been previously reported with the hemostatic mechanism, which part of HNP-1 facilitates the hemostatic activity is not known. Here, a partial peptide (HNP-F) promoting hemostasis, originating from HNP-1, has been newly identified by the blood coagulation ability test. HNP-F shows the best hemostatic effect between the anterior half and posterior half of peptides. Moreover, microscopic images show platelet aggregation and an increase in the concentration of platelet factor 4, and the scanning electron microscope image of platelets support platelet activation by HNP-F. Thromboelastography indicates decreased clotting time and increased physical properties of blood clotting. Mouse liver experiments demonstrate improved hemostatic effect by treatment of peptide solution. Cell viability and hemolysis assays confirm the HNP-F's biosafety. It is hypothesized that the surface charge and structure of HNP-F could be favorable to interact with fibrinogen or thrombospondin-1. Collectively, because HNP-F as an active peptide hemostat has many advantages, it could be expected to become a potent hemostatic biomaterial, additive or pharmaceutical candidate for various hemostatic applications.

Keywords: blood coagulation; hemostat; human neutrophil peptides; platelet activation; therapeutics.

MeSH terms

  • Animals
  • Cell Survival / drug effects
  • Hemolysis / drug effects
  • Hemostasis / drug effects*
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Peptide Fragments / chemistry
  • Peptide Fragments / genetics
  • Peptide Fragments / pharmacology
  • Thrombelastography
  • alpha-Defensins* / chemistry
  • alpha-Defensins* / genetics
  • alpha-Defensins* / pharmacology

Substances

  • Peptide Fragments
  • alpha-Defensins
  • human neutrophil peptide 1