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(Circulation Research. 1999;85:992.)
© 1999 American Heart Association, Inc.

Molecular Medicine

Vascular Endothelial Growth Factor (VEGF) and VEGF-C Show Overlapping Binding Sites in Embryonic Endothelia and Distinct Sites in Differentiated Adult Endothelia

Athina Lymboussaki¹, Birgitta Olofsson¹, Ulf Eriksson, Kari Alitalo

From the Molecular/Cancer Biology Laboratory (A.L., K.A.), Haartman Institute, University of Helsinki, Finland, and Ludwig Institute for Cancer Research (B.O., U.E.), Stockholm, Sweden.

Correspondence to Dr Kari Alitalo, Molecular/Cancer Biology Laboratory, Haartman Institute, POB 21 (Haartmaninkatu 3), University of Helsinki, 00014 Finland. E-mail kari.alitalo{at}helsinki.fi

Abstract—Vascular endothelial growth factor (VEGF) is a key modulator of angiogenesis during development and in adult tissues, whereas the related VEGF-C has been shown to induce both lymphangiogenesis and angiogenesis. To better understand the specific functions of these growth factors, we have here analyzed their binding to sections of mouse embryonic and adult tissues and compared the distribution of the bound growth factors with the expression patterns of the 3 known members of the VEGF receptor family as well as with neuropilin-1, a coreceptor for VEGF₁₆₅. Partially overlapping patterns of VEGF and VEGF-C binding were obtained in embryonic tissues, consistent with the expression of all known VEGF receptors by vascular endothelial cells. However, the most striking differences of binding were observed in the developing and adult heart, in which VEGF decorated all vessels, whereas strong VEGF-C signals were obtained only from epicardial vessels. In the lymph nodes, VEGF and VEGF-C showed distinct binding patterns in agreement with the differential location of their specific receptors. These results show that both VEGF-C and VEGF target embryonic blood vessels, whereas a more selective binding of VEGF-C occurs to its lymphatic vascular receptor in certain adult tissues. Our results suggest that VEGF and VEGF-C have both overlapping and distinct activities via their endothelial receptors.

Key Words: angiogenesis • vascular endothelial growth factor receptor • lymphatic vessel

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