Abstract

Adipose tissue is traditionally categorized into white and brown relating to their function and morphology. The classical white adipose tissue builds up energy in the form of triglycerides and is useful for preventing fatigue during periods of low caloric intake and the brown adipose tissue more energetically active, with a greater number of mitochondria and energy production in the form of heat. Since adult humans possess significant amounts of active brown fat depots and its mass inversely correlates with adiposity, brown fat might play an important role in human obesity and energy homeostasis. New evidence suggests two types of thermogenic adipocytes with distinct developmental and anatomical features: classical brown adipocytes and beige adipocytes. Beige adipocyte has recently attracted special interest because of its ability to dissipate energy and the possible ability to differentiate themselves from white adipocytes. The presence of brown and beige adipocyte in human adults has acquired attention as a possible therapeutic intervention for metabolic diseases. Importantly, adult human brown appears to be mainly composed of beige-like adipocytes, making this cell type an attractive therapeutic target for obesity and obesity-related diseases, such as atherosclerosis, arterial hypertension and diabetes mellitus type 2. Because many epigenetics changes can affect beige adipocyte differentiation from adipose progenitor cells, the knowledge of the circumstances that affect the development of beige adipocyte cells may be important to new pathways in the treatment of metabolic diseases. New molecules have emerged as possible therapeutic targets, which through the impulse to develop beige adipocytes can be useful for clinical studies. In this review will discuss some recent observations arising from the unique physiological capacity of these cells and their possible role as ways to treat obesity and diabetes mellitus type 2.

Highlights

  • Diabetes mellitus type 2 (DM2) is a chronic disease, the incidence of which has increased dramatically in recent years

  • Adipocytes are derived from mesenchymal stem cells (MSCs), which can be neuroectodermal or mesodermal depending on where the fat body originates; differentiation of adipocytes requires a committed pre-adipocyte progenitor [32]

  • It has been described that some beige adipocytes are myosin heavy chain 11 (Myh11)-positive, which is a selective marker of smooth muscle cells [45]. All of these results indicate that beige adipocytes have a cellular origin different from the classical brown adipocyte

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Summary

Introduction

Diabetes mellitus type 2 (DM2) is a chronic disease, the incidence of which has increased dramatically in recent years. Given that obesity and DM2 have precise events in common, such as energy balance, stimulation of thermogenesis and calorie expenditure, a possible therapeutic strategy could be the manipulation of the adipose tissue that controls the balance between the accumulation of energy and the production of heat. Utilizing these parameters, from this perspective, the treatment of DM2 and obesity could be through the modulation of the physiology of the adipocyte precursors [15]. Extracellular signals include the activation of the sympathetic nervous system, the cells of the immune system and epigenetic variations [30] that influence the transcription of specific genes [31]

The Origin of Adipocytes
Beige Thermogenesis
Epigenetic Regulation by DNA Methylation
Epigenetics and Mechanisms of Chromatin Modification
Epigenetics Changes by Non-Coding RNA
Induction of Beige Adipocyte by Cold
Influence of Physical Exercise
Role of Interleukins
Endocrine Factors and Metabolites in Beige Adipocytes
Findings
10. Potential Therapeutic Use in Humans
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