This Article Full Text Full Text (PDF) All Versions of this Article: 0008-5472.CAN-08-4539v1 69/10/4537    most recent Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Chang, S.-H. Articles by Dvorak, H. F. Search for Related Content PubMed PubMed Citation Articles by Chang, S.-H. Articles by Dvorak, H. F.

VEGF-A Induces Angiogenesis by Perturbing the Cathepsin-Cysteine Protease Inhibitor Balance in Venules, Causing Basement Membrane Degradation and Mother Vessel Formation

Departments of ¹ Pathology and ² Medicine, and the Center for Vascular Biology Research, Beth Israel Deaconess Medical Center and Harvard Medical School, and ³ Departments of Surgery, Children's Hospital and Harvard Medical School, Boston, Massachusetts; ⁴ Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, New York, New York; and ⁵ Department of Pathology, Stanford University, Stanford, California

Requests for reprints: Harold F. Dvorak, Department of Pathology, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, RN 227C, Boston, MA 02215. Phone: 617-667-0654; Fax: 617-667-2913; E-mail: hdvorak{at}bidmc.harvard.edu.

Key Words: cathepsins • cysteine protease inhibitor • VEGF • angiogenesis • mother vessels

Tumors initiate angiogenesis primarily by secreting vascular endothelial growth factor (VEGF-A¹⁶⁴). The first new vessels to form are greatly enlarged, pericyte-poor sinusoids, called mother vessels (MV), that originate from preexisting venules. We postulated that the venular enlargement necessary to form MV would require a selective degradation of their basement membranes, rigid structures that resist vascular expansion. To identify the specific proteases responsible for MV formation, we induced angiogenesis in mouse tissues with an adenoviral vector expressing VEGF-A¹⁶⁴ (Ad-VEGF-A¹⁶⁴) or with VEGF-A–secreting TA3/St mammary tumors. We found that MV formation resulted from greatly increased activity of cathepsins (B>S>L) in venules transitioning into MV, as well as from a reciprocal decrease in the expression of several cysteine protease inhibitors (CPI), stefin A and cystatins B and C, by these same venules. Using a fluorescence probe that selectively binds cellular sites of cathepsin protease activity in vivo, we showed that increased cathepsin activity was localized exclusively to perivenular cells, not to venule endothelial cells. CPI strikingly inhibited angiogenesis in the Matrigel assay, and Ad-VEGF-A¹⁶⁴–induced angiogenesis was reduced by 50% in cathepsin B–null mice. Thus, VEGF-A, whether expressed by interstitial cells infected with an adenoviral vector or by tumor cells, upsets the normal cathepsin-CPI balance in nearby venules, leading to degradation of their basement membranes, an important first step in angiogenesis. [Cancer Res 2009;69(10):4537–44]