期刊
FEBS JOURNAL
卷 276, 期 20, 页码 5738-5746出版社
WILEY
DOI: 10.1111/j.1742-4658.2009.07303.x
关键词
adipokine; adiponectin; angiogenesis; endothelial cell; hypoxia; inflammation; lymphangiogenesis; lymphatic; permeability
资金
- NIH [R01-DK55758, R24-DK071030-01, R01-CA112023, T32-HL007360-31A1, F32-DK081279]
- NATIONAL CANCER INSTITUTE [R01CA112023] Funding Source: NIH RePORTER
- NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [T32HL007360] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK055758, R24DK071030, F32DK081279] Funding Source: NIH RePORTER
Adipose tissue is an endocrine organ made up of adipocytes, various stromal cells, resident and infiltrating immune cells, and an extensive endothelial network. Adipose secretory products, collectively referred to as adipokines, have been identified as contributors to the negative consequences of adipose tissue expansion that include cardiovascular disease, diabetes and cancer. Systemic blood circulation provides transport capabilities for adipokines and fuels for proper adipose tissue function. Adipose tissue microcirculation is heavily impacted by adipose tissue expansion, some adipokines can induce endothelial dysfunction, and angiogenesis is necessary to counter hypoxia arising as a result of tissue expansion. Tumors, such as invasive lesions in the mammary gland, co-opt the adipose tissue microvasculature for local growth and metastatic spread. Lymphatic circulation, an area that has received little metabolic attention, provides an important route for dietary and peripheral lipid transport. We review adipose circulation as a whole and focus on the established and potential interplay between adipose tissue and the microvascular endothelium.
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