FEBS Letters
Volume 582, Issue 17 , Pages 2515-2520, 23 July 2008

Neostatin-7 regulates bFGF-induced corneal lymphangiogenesis

Edited by Veli-Pekka Lehto

Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, 1855 West Taylor Street, Chicago, IL 60612, USA

Received 4 April 2008; received in revised form 16 May 2008; accepted 10 June 2008. published online 19 June 2008.

Abstract 

Neostatin-7, with an anti-angiogenic potential, is generated from the proteolytic action of matrix metalloproteinase-7 on collagen XVIII. We previously reported that neostatin-7 inhibited angiogenesis in vitro and in vivo. Here we demonstrate that neostatin-7/collagen XVIII may possess anti-lymphangiogenic activities by: (1) corneal micropellet implantation of neostatin-7 reduced bFGF-induced corneal lymphangiogenesis; (2) neostatin-7 bound to VEGF receptor-3 in vitro; and (3) enhanced corneal lymphangiogenesis and VEGF-C expression in collagen XVIII knockout mice in a corneal wounding model. Understanding the mechanism of neostatin-7/collagen XVIII on corneal lymphangiogenesis may provide therapeutic interventions to treat lymphangiogenesis-related disorders, such as lymphedema, transplantation rejection and cancers.

Keywords: Collagen XVIII, Neostatin-7, Endostatin, Lymphangiogenesis, bFGF

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 Supported by EY01792, EY10101 (D.T.A.), NIH EY14048 (J.H.C.), the Illinois Society for the Prevention of Blindness, and Research to Prevent Blindness Grant.

PII: S0014-5793(08)00504-8

doi:10.1016/j.febslet.2008.06.014

FEBS Letters
Volume 582, Issue 17 , Pages 2515-2520, 23 July 2008