Histidine-proline-rich glycoprotein has potent antiangiogenic activity mediated through the histidine-proline-rich domain

Jose C. Juarez, Xiaojun Guan, Natalya V. Shipulina, Marian L. Plunkett, Graham C. Parry, David Elliot Shaw, Jing Chuan Zhang, Shafaat A. Rabbani, Keith R. McCrae, Andrew P. Mazar, William T. Morgan, Fernando Doñate

Research output: Contribution to journalArticlepeer-review

83 Scopus citations

Abstract

Histidine-proline-rich glycoprotein (HPRG) is an abundant multi-domain plasma protein evolutionarily related to high-molecular-weight kininogen. The cleaved form of high-molecular-weight kininogen has recently been demonstrated to exhibit antiangiogenic activities in vitro (J. C. Zhang et al., FASEB J., 14: 2589-2600, 2000), mediated primarily through domain 5. HPRG contains a histidine-proline-rich (H/P) domain with sequence and functional similarities to HKa-D5. We hypothesized that HPRG may also have antiangiogenic properties, localized within its H/P domain. The H/P domain is highly conserved among species, and because rabbit H/P domain is more resistant to internal proteolytic cleavage than the human domain, the rabbit HPRG (rbHPRG) was primarily used to assess the antiangiogenic activity of HPRG. Rabbit HPRG inhibited human umbilical vein endothelial cell (HUVEC) tube formation stimulated by fibroblast growth factor-2 (FGF-2) or vascular endothelial growth factor on a Matrigel surface as well as cell proliferation of FGF-2 stimulated HUVECs. The antiangiogenic activity of rbHPRG was localized to the H/P domain by use of proteolytic fragments of rbHPRG and was further confirmed and characterized in two in vivo models of angiogenesis: the chorioallantoic membrane of the chick assay and the mouse Matrigel plug assay. Caspase-3 activation was observed in HUVECs stimulated with FGF-2 in the presence of rbHPRG, suggesting that apoptosis of activated endothelial cells may be one of the mechanisms underlying its antiangiogenic activity. Finally, the H/P domain of rbHPRG reduced tumor cell number when tumor cells were co-inoculated in the Matrigel plug assay. In conclusion, the H/P domain within HPRG induces the apoptosis of activated endothelial cells leading to potent antiangiogenic effects.

Original languageEnglish (US)
Pages (from-to)5344-5350
Number of pages7
JournalCancer Research
Volume62
Issue number18
StatePublished - Sep 15 2002

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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