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White-to-Beige and Back: Adipocyte Conversion and Transcriptional Reprogramming.

作者信息

Boychenko Stanislav, Egorova Vera S, Brovin Andrew, Egorov Alexander D

机构信息

Gene Therapy Department, Center for Translational Medicine, Sirius University of Science and Technology, 354340 Sirius, Russia.

Biotechnology Department, Center for Translational Medicine, Sirius University of Science and Technology, 354340 Sirius, Russia.

出版信息

Pharmaceuticals (Basel). 2024 Jun 16;17(6):790. doi: 10.3390/ph17060790.


DOI:10.3390/ph17060790
PMID:38931457
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11206576/
Abstract

Obesity has become a pandemic, as currently more than half a billion people worldwide are obese. The etiology of obesity is multifactorial, and combines a contribution of hereditary and behavioral factors, such as nutritional inadequacy, along with the influences of environment and reduced physical activity. Two types of adipose tissue widely known are white and brown. While white adipose tissue functions predominantly as a key energy storage, brown adipose tissue has a greater mass of mitochondria and expresses the uncoupling protein 1 () gene, which allows thermogenesis and rapid catabolism. Even though white and brown adipocytes are of different origin, activation of the brown adipocyte differentiation program in white adipose tissue cells forces them to transdifferentiate into "beige" adipocytes, characterized by thermogenesis and intensive lipolysis. Nowadays, researchers in the field of small molecule medicinal chemistry and gene therapy are making efforts to develop new drugs that effectively overcome insulin resistance and counteract obesity. Here, we discuss various aspects of white-to-beige conversion, adipose tissue catabolic re-activation, and non-shivering thermogenesis.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79af/11206576/c1ffbe57c208/pharmaceuticals-17-00790-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79af/11206576/6d0712244337/pharmaceuticals-17-00790-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79af/11206576/86a8d189b014/pharmaceuticals-17-00790-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79af/11206576/c1ffbe57c208/pharmaceuticals-17-00790-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79af/11206576/6d0712244337/pharmaceuticals-17-00790-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79af/11206576/86a8d189b014/pharmaceuticals-17-00790-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79af/11206576/c1ffbe57c208/pharmaceuticals-17-00790-g003.jpg

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本文引用的文献

[1]
Coffee, tea, and cocoa in obesity prevention: Mechanisms of action and future prospects.

Curr Res Food Sci. 2024-4-20

[2]
Adipose tissue macrophages secrete small extracellular vesicles that mediate rosiglitazone-induced insulin sensitization.

Nat Metab. 2024-5

[3]
Worldwide trends in underweight and obesity from 1990 to 2022: a pooled analysis of 3663 population-representative studies with 222 million children, adolescents, and adults.

Lancet. 2024-3-16

[4]
Adults with metabolically healthy overweight or obesity present more brown adipose tissue and higher thermogenesis than their metabolically unhealthy counterparts.

EBioMedicine. 2024-2

[5]
Bisphenol S induces brown adipose tissue whitening and aggravates diet-induced obesity in an estrogen-dependent manner.

Cell Rep. 2023-12-26

[6]
Adipose tissue browning and thermogenesis under physiologically energetic challenges: a remodelled thermogenic system.

J Physiol. 2024-1

[7]
State-of-the-art review of theabrownins: from preparation, structural characterization to health-promoting benefits.

Crit Rev Food Sci Nutr. 2024-11

[8]
Adipose Tissue and Metabolic Health.

Diabetes Metab J. 2023-9

[9]
Deficiency of Adipose Aryl Hydrocarbon Receptor Protects against Diet-Induced Metabolic Dysfunction through Sexually Dimorphic Mechanisms.

Cells. 2023-6-29

[10]
Resveratrol inhibits AhR/Notch axis and reverses Th17/Treg imbalance in purpura by activating Foxp3.

Toxicol Res (Camb). 2023-4-20

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