A serum-free in vitro model of renal microvessel development

Author:

Antes Lisa M.1,Villar Monica M.1,Decker Sylvia2,Nicosia Roberto F.3,Kujubu Dean A.1

Affiliation:

1. Renal-Electrolyte and Hypertension Division, Department of Medicine, Philadelphia Veterans Affairs Medical Center and University of Pennsylvania School of Medicine;

2. Center for Oral Health Research, University of Pennsylvania School of Dental Medicine, Philadelphia 19104; and

3. Department of Pathology, Allegheny University of the Health Sciences, Philadelphia, Pennsylvania 19102

Abstract

The differentiation and organization of the embryonic renal vasculature is a crucial event in renal development. To study this process, we developed a serum-free in vitro model of renal microvessel development. Mouse embryonic kidney explants, when embedded specifically in type I collagen, demonstrate outgrowth of microvascular structures when stimulated by the phorbol ester 12- O-tetradecanoylphorbol 13-acetate (TPA, 10–50 ng/ml). Other polypeptide growth factors stimulated little, if any, microvessel outgrowth from the explants. Similar outgrowths were not observed when other embryonic tissue explants were used. The number of microvessels observed depended on the gestational age of the explants. We hypothesize that TPA induces the in situ differentiation of metanephric mesenchymal cells into endothelial cell precursors and that specific matrix proteins and cell-matrix interactions are necessary for the organization of these precursors into microvessels. Our model will allow us to examine in detail the responsiveness of metanephric kidney cells to both growth factors and extracellular matrix molecules and to understand how they influence renal endothelial cell differentiation.

Publisher

American Physiological Society

Subject

Physiology

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A Model for ex vivo Renal Angiogenesis;Nephron Experimental Nephrology;2003

2. Microvessel formation from mouse embryonic aortic explants is oxygen and VEGF dependent;American Journal of Physiology-Regulatory, Integrative and Comparative Physiology;2002-08-01

3. THE SPECIFICITY OF PHENOTYPIC INDUCTION OF MOUSE AND HUMAN STEM CELLS BY SIGNALING COMPLEXES;In Vitro Cellular & Developmental Biology - Animal;2002

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