机构:
Tech Univ Dresden, Fac Med, Div Med Biol, Dept Psychiat, Dresden, Germany
Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Dresden, GermanyTech Univ Dresden, Fac Med, Div Med Biol, Dept Psychiat, Dresden, Germany
Breier, Georg
[1
,2
]
Chavakis, Triantafyllos
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机构:
Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Dresden, Germany
Tech Univ Dresden, Fac Med, Inst Clin Chem & Lab Med, Dresden, GermanyTech Univ Dresden, Fac Med, Div Med Biol, Dept Psychiat, Dresden, Germany
Chavakis, Triantafyllos
[2
,3
]
Hirsch, Emilio
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Univ Torino, Dept Mol Biotechnol & Hlth Sci, Turin, ItalyTech Univ Dresden, Fac Med, Div Med Biol, Dept Psychiat, Dresden, Germany
Hirsch, Emilio
[4
]
机构:
[1] Tech Univ Dresden, Fac Med, Div Med Biol, Dept Psychiat, Dresden, Germany
[2] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Dresden, Germany
Angiogenesis, literally formation of new blood vessels, is the main process through which the vascular system expands during embryonic and postnatal development. Endothelial cells, which constitute the inner lining of all blood vessels, are typically in a quiescent state in the healthy adult organism. However, in vascular and metabolic diseases, the endothelium becomes unstable and dysfunctional. The resulting tissue hypoxia may thereby induce pathological angiogenesis, which is a hallmark of disease conditions like cancer or diabetic retinopathy. However, recent evidence suggests that angiogenesis is also a major player in the context of further metabolic diseases, especially in obesity. In particular, deregulated angiogenesis is linked with adipose tissue dysfunction and insulin resistance. On the other hand, signalling pathways, such as the PI3K pathway, may regulate metabolic activities in the endothelium. Endothelial cell metabolism emerges as an important regulator of angiogenesis. This review summarises the role of angiogenesis in metabolic-vascular disease, with specific focus on the role of angiogenesis in obesity-related metabolic dysfunction and on signaling pathways, especially PI3K, linking cell metabolism to endothelial function.
机构:
Dartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Angiogenesis Res Ctr, Lebanon, NH 03756 USA
Dartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Vasc Sect, Dept Med, Lebanon, NH 03756 USADartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Angiogenesis Res Ctr, Lebanon, NH 03756 USA
Mulligan-Kehoe, Mary Jo
Simons, Michael
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机构:
Dartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Angiogenesis Res Ctr, Lebanon, NH 03756 USA
Dartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Cardiol Sect, Dept Med, Lebanon, NH 03756 USA
Dartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Dept Pharmacol & Toxicol, Lebanon, NH 03756 USADartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Angiogenesis Res Ctr, Lebanon, NH 03756 USA
机构:
Tech Univ Dresden, Med Klin 3, Univ Klinikum Carl Gustav Carus, Dresden, GermanyTech Univ Dresden, Med Klin 3, Univ Klinikum Carl Gustav Carus, Dresden, Germany
Hanefeld, M.
Saad, F.
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机构:
Tech Univ Dresden, Med Klin 3, Univ Klinikum Carl Gustav Carus, Dresden, GermanyTech Univ Dresden, Med Klin 3, Univ Klinikum Carl Gustav Carus, Dresden, Germany