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Fig. 1 | Journal of Translational Medicine

Fig. 1

From: The role of DGAT1 and DGAT2 in regulating tumor cell growth and their potential clinical implications

Fig. 1

Biogenesis and functions of Lipid droplets. The biogenesis of Lipid droplets (LDs) in normal and tumor cells is a complex process, consisting of multiple steps, briefly including neutral lipid synthesis and lens formation, lipid droplet bidding, lipid droplet growth and maturation and protein targeting to lipid droplets [19]. The whole process of LD biogenesis occurs in the endoplasmic reticulum (ER) and the essential enzymes catalyzed synthesis of neutral lipids, including diacylglycerol acyltrans-ferases (DGATs) and acyl-CoA:cholesterol O-acyltransferases (ACATs) also located in the ER [19]. The first step is synthesis of neutral lipids (triacylglycerols and sterol esters) between the leaflets of the ER bilayer [21]. Accompanied by the deposit and incrased concentration of neutral lipids, an oil lens is formated in a process of demixing when the concentration of triacylglycerol is in the range of 5–10 mol% [19]. Under the regulation of ER membrane phospholipid and membrane surface tension, the LD budding is observed as a result of expansion of the neutral lipid lens. Through droplet–droplet fusion, LDs expand and a population of LDs eventually detaches from the ER in higher eukaryotes. Upon fusion, integral membrane proteins such as DGAT2, are able to diffuse from the ER to LDs, whereas the DGAT1 only exists in ER. Finally, up to 100–200 proteins, dominated by enzymes involved in lipid metabolism and members of the peri-lipin family target to LDs to endow LDs with dynamic and complex functions [15]

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