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Soluble Egg Antigens fromSchistosoma mansoniInduce Angiogenesis‐Related Processes by Up‐Regulating Vascular Endothelial Growth Factor in Human Endothelial Cells
Author(s) -
David A. Loeffler,
Steven K. Lundy,
Kameshwar P. Singh,
Hervé C. Gérard,
Alan P. Hudson,
Dov L. Boros
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/340416
Subject(s) - angiogenesis , schistosoma mansoni , vascular endothelial growth factor , biology , endothelial stem cell , umbilical vein , immunology , microbiology and biotechnology , growth factor , vascular endothelial growth factor a , schistosomiasis , in vitro , cancer research , biochemistry , vegf receptors , receptor , helminths
Schistosomiasis mansoni is characterized by hepatic granuloma formation. Endothelial cell activation within these granulomas may contribute to their development and to increased vascularization in the granuloma periphery. The earliest event in granuloma formation is the lodging of schistosome eggs within presinusoidal capillaries. The eggs secrete factors that may activate endothelial cells. This study investigated the effects of Schistosoma mansoni soluble egg antigen (SEA) on angiogenic processes: proliferation, tube formation, and apoptosis of human umbilical vein endothelial cells (HUVECs). HUVECs require serum and growth factors to proliferate in vitro. Proliferation occurred when SEA or live eggs were substituted for growth factors, but not for serum. SEA increased HUVEC tube formation and decreased HUVEC apoptosis after serum and growth factor deprivation. Messenger RNA for vascular endothelial growth factor (VEGF) increased 2-fold in SEA-treated HUVECs. These findings suggest that products secreted by schistosome eggs may promote angiogenesis within hepatic granulomas by up-regulating endothelial cell VEGF.

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