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Angiogenesis in Balb/c mice under beta-carotene supplementation in diet
Authors:Urszula Razny  Anna Polus  Beata Kiec-Wilk  Lukasz Wator  Jadwiga Hartwich  Jerzy Stachura  Romana Tomaszewska  Grzegorz Dyduch  Piotr Laidler  Gerd Schmitz  Regina Goralczyk  Karin Wertz  George Riss  Nicole L. W. Franssen-van Hal  Jaap Keijer  Aldona Dembinska-Kiec
Affiliation:1. Department of Clinical Biochemistry, Jagiellonian University Medical College, Kopernika 15a Street, 31-501, Cracow, Poland
2. Department of Pathomorphology, Jagiellonian University Medical College, Grzegorzecka 16 Street, 31-531, Cracow, Poland
3. Department of Medical Biochemistry, Jagiellonian University Medical College, Kopernika 7 Street, 31-034, Cracow, Poland
4. Department of Clinical Chemistry, Laboratory Medicine and Transfusiology, University of Regensburg, Franz-Josef-Strauss-Allee 11, 93042, Regensburg, Germany
5. DSM Nutritional Products, Human Nutrition and Health, Carotenoid Section, Building 241, P.O. Box 2676, 4002, Basel, Switzerland
6. Food Bioactives Group, RIKILT, Institute of Food Safety, P.O. Box 338, 6700 AH, Wageningen, The Netherlands
7. Human and Animal Physiology, Animal Sciences, Wageningen University, Marijkeweg 40 (building 531), P.O. box 338, 6700 AH, Wageningen, The Netherlands
Abstract:Angiogenesis is a process of new blood vessel formation from pre-existing ones. The most important steps in angiogenesis include detachment, proliferation, migration, homing and differentiation of vascular wall cells, which are mainly endothelial cells and their progenitors. The study focused on the effect of beta-carotene (BC) supplementation (12,000 mg/kg) in the diet on angiogenesis in Balb/c mice. Female Balb/c mice were fed for 5 weeks with two different diets: with BC or without BC supplementation. After 4 weeks of feeding, Balb/c mice were injected subcutaneously with two matrigel plugs with or without basic fibroblast growth factor (bFGF). Six days later, the animals were killed, and the matrigel plugs were used for immunohistochemical staining with CD31 antibody and for gene expression analysis. Microarray and Real-Time PCR data showed down-regulation of genes involved in proliferation and up-regulation of genes encoding inhibitors of apoptosis, proteins regulating cell adhesion, matrix-degrading enzymes and proteins involved in the VEGF pathway. The results of this study demonstrated that BC proangiogenic activity (with or without bFGF) in vivo seemed to be more significantly associated with cells’ protection from apoptosis and their stimulation of chemotaxis/homing than cell proliferation.
Keywords:Angiogenesis   Beta-carotene   Chemotaxis   Microarray
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