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Blood vessels can make you fat, and yet fit: Healthy obesity begins where metabolic disorders emerge

- Vascular-adipose interaction enables a selective fat storage in a healthier way -

Can obesity define health? It is a question for much debate. Still, obesity is generally classified into metabolically healthy obesity (MHO) and an unhealthy version of obesity. As we grow older, we tend to put on excess fat more around the waist than the hips and legs with aging, becoming more “apple-shaped” than “pear-shaped” and also at a greater risk of metabolic syndrome. As fat accumulates around our abdominal organs, instead of under the skin where most of our body fat usually sits, this visceral fat releases fatty acids and inflammatory substances directly into the liver, causing toxicity and insulin resistance. People with MHO, meanwhile are characterized by favorable health parameters, including high insulin sensitivity, no signs of hypertension, and less inflammation, and a healthier immune system.

Figure 1 Expression of fatty acid transporters in blood vessels.
▲ Figure 1 Expression of fatty acid transporters in blood vessels.Fatty acid transporters (CD36; blue) in blood vessels (green), whose overlapping shown in yellow green, transverse around fat cells (red) under the skin.

It is undeniable that where body fat sits matters for health, but little has been known about what mechanism determines whether we have the pear shape or the apple shape. Led by Dr. KOH Gou Young at the Center for Vascular Research, within the Institute for Basic Science (IBS), South Korea, scientists have reported Angiopoietin-2 (Angpt2) – a hormone secreted from fat tissue, previously known as a protein coding peptide involved in embryonic vascular development – as a key driver that inhibits the accumulation of potbellies by enabling the proper transport of fatty acid into general circulation in blood vessels, thus preventing insulin resistance. Their findings have been published online in the journal Nature Communications (12 June 2020).

“Previous approaches blocked the expression of Angpt2 in the whole circulatory system with pharmacological interventions to inhibit displaced fat accumulation that leads to metabolic disorders. Though the vascular endothelial cell is the anatomic and metabolic gatekeeper of fat shuttling into tissues, it has still remained uncertain whether the displaced accumulation of excess fat in fat tissues is a cause or an indicator of metabolic syndrome. We specifically focused on the fatty acid shuttling in the specific fat tissues under the skin. Angpt2 is found to play a key role in packing on fat on proper locations where they should be to contain wider waistline,” says BAE Hosung, the first author of this study.

Noting that the blood vessels under the skin are home to certain fatty acid transport proteins, the researchers compared samples from MHO and metabolically unhealthy obese individuals. Angpt2 turned out to be the single potential candidate for sustaining metabolic health via regulation of body fat distribution. Through various tissue-specific knock out mouse models and mechanistic studies in primary cultured cells, they revealed Angpt2 produced from fat cells interacts with its receptor integrin α5β1 to drive fatty acid transporters and ensure normal distribution of circulating fat. “Intriguingly, Angpt2–integrin α5β1 signaling took just few minutes. This near-instant processing makes sense since this biological mechanism should cope with the surge of fat levels in the blood after a meal,” explains Bae.

Figure 2 Endothelial-to-adipocyte fatty acid transport determines metabolic health.
▲ Figure 2 Endothelial-to-adipocyte fatty acid transport determines metabolic health.Angpt2 produced from fat cells interacts with its receptor integrin α5β1 to drive fatty acid transporters (CD36 and FATP3) and ensures normal circulating fat. If this Angpt2–integrin α5β1 signaling does not work, defects in buffering capacity of fat tissue lead to fat spillover into the liver and muscle, convert brown fat to white fat, and consequently result in defects in metabolic health.

The inhibition of this process triggered fat accumulation in other fat depots and abdominal organs, leading to systemic glucose intolerance, which is reminiscent of the pattern in metabolically unhealthy obese patients.

Figure 3 Depletion of Angiopoietin-2 from fat cells drives fat accumulation in other fat depots and abdominal organs.
▲ Figure 3 Depletion of Angiopoietin-2 from fat cells drives fat accumulation in other fat depots and abdominal organs.Representative images of morphology and fat accumulation into the liver (left) and muscle (right) in wild type and adipocyte-specific Angpt2 knockout mice. Fat accumulation in adipocyte-specific Angpt2 knockout mice could be observed in white spots (top), red oil staining (middle), and green fatty acid intensity (bottom).

Can Angpt2 treatment be a therapeutic strategy to normalize fat distribution and treat obesity-induced metabolic disorders? As shown in previous efforts, systemic modulation of Angpt2 through pharmacological blockade is limited as Angpt2 is individual, and it depends on heterogeneity of different fat depots. Alternatively, activating integrin receptors or fatty acid transporters may be a more feasible approach for its relatively restricted expression in fat cells under the skin. “It requires further investigation to test these possibilities genetically or pharmaceutically to open new therapeutic paths for transformation of metabolically unhealthy obesity to healthy obesity,” adds Bae.

KIM Dahee Carol
IBS Communications Team

Notes for editors

- References
Hosung Bae, Ki Yong Hong, Choong-kun Lee, Cholsoon Jang, Seung-Jun Lee, Kibaek Choe, Stefan Offermanns, Yulong He, Hyuek Jong Lee, and Gou Young Koh. Angiopoietin-2–integrin α5β1 signaling enhances vascular fatty acid transport and prevents ectopic lipid–induced insulin resistance. Nature Communications (2020 June). DOI: 10.1038/s41467-020-16795-4

- Media Contact
For further information or to request media assistance, please contact Dr. Hosung Bae (+82-42-350-4271, hstbae@ibs.re.kr); or Mr. Daewoong Bae, Head of IBS Communications Team (+82-42-878-8195, woongs@ibs.re.kr); or Ms. Dahee Carol Kim, Public Information Officer of IBS & Science Communicator (+82-42-878-8133, clitie620@ibs.re.kr)

- About the Institute for Basic Science (IBS)
IBS was founded in 2011 by the government of the Republic of Korea with the sole purpose of driving forward the development of basic science in South Korea. IBS has 30 research centers as of January 2020. There are ten physics, two mathematics, six chemistry, six life science, one Earth science, and five interdisciplinary research centers.

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    Last Update 2023-11-28 14:20