Human histidine-rich glycoprotein expressed in SF9 insect cells inhibits apatite formation

FEBS Lett. 1997 Aug 4;412(3):559-62. doi: 10.1016/s0014-5793(97)00827-2.

Abstract

Histidine-rich glycoprotein (HRG) is structurally related to the alpha2-HS glycoprotein/fetuin family of mammalian plasma proteins; both belong to the cystatin superfamily of proteins. We expressed recombinant human HRG and alpha2-HS in Sf9 insect cells for functional analysis. Recombinant HRG bound heparin and fibrinogen while alpha2-HS did not. Both proteins inhibited the formation of apatite, recombinant HRG (IC50 approximately 1 microM) with 2-fold lower molar activity than alpha2-HS (IC50 approximately 0.5 microM). The inhibition in vitro of apatite formation suggests a new function for plasma HRG protein, inhibition of phase separation in blood vessels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apatites / antagonists & inhibitors*
  • Apatites / metabolism
  • Blood Proteins / biosynthesis
  • Blood Proteins / genetics
  • Blood Proteins / metabolism
  • Bone and Bones / metabolism
  • Cell Line
  • Heparin / metabolism
  • Humans
  • Protein Binding
  • Protein Biosynthesis*
  • Proteins / genetics
  • Proteins / pharmacology*
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / pharmacology
  • Spodoptera
  • alpha-2-HS-Glycoprotein

Substances

  • AHSG protein, human
  • Apatites
  • Blood Proteins
  • Proteins
  • Recombinant Proteins
  • alpha-2-HS-Glycoprotein
  • histidine-rich proteins
  • Heparin