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Adipose Differentiation-Related Protein (ADRP)

ADRP/ADFP, the major lipid droplet protein, is capable of sequestering TG in the cytosol, diverting it from entering into ER lumen for VLDL secretion. ADFP is involved in LD formation and/or maturation. Macrophages play an important role in atherosclerosis. An earlyevent in atherosclerosis is the accumulation of LDs in lesionalmacrophages associated with ADFP accumulation. ADFP is the most abundant LD-associated protein found in these cells. Modified lipoproteins, e.g., oxidized LDL or acetylated LDL, that arehighly atherogenic upregulate Adfp expression in macrophagesin vitro . Furthermore, Adfp mRNA is upregulated in human atherosclerotic plaques compared with lesion-free areas of thesame arteries . Conversely, ADFP overexpression in THP-1macrophage enhances lipid accumulation and prevents lipid efflux.These results suggest that ADFP is potentially a proatherosclerogenic protein. Our preliminary study using Adfp-deficient mice seems to support this notion. ADFP is the predominant LD-associated protein in skeletal musclein humans . Furthermore, muscle ADFP is lower in insulin-resistant subjects, a situation that can be reversed by weight reduction or by troglitazone treatment coincident with an improvement in glucose tolerance. It is possible that the upregulation of ADFP may help sequester fatty acids as TG in LDs, protecting the muscle from the detrimental effects of fatty acids on insulinaction and glucose homeostasis . Chang BHJ et al. Am J Physiol Gastrointest Liver Physiol 292: G1465-G1468, 2007

Synonyms

  • Adipophilin
  • ADFP
Human ADRP, 437 amino acids, MW 48074 Da
        10         20         30         40         50         60   
MASVAVDPQP SVVTRVVNLP LVSSTYDLMS SAYLSTKDQY PYLKSVCEMA ENGVKTITSV 
        70         80         90        100        110        120   
AMTSALPIIQ KLEPQIAVAN TYACKGLDRI EERLPILNQP STQIVANAKG AVTGAKDAVT     
       130        140        150        160        170        180   
TTVTGAKDSV ASTITGVMDK TKGAVTGSVE KTKSVVSGSI NTVLGSRMMQ LVSSGVENAL      
       190        200        210        220        230        240   
TKSELLVEQY LPLTEEELEK EAKKVEGFDL VQKPSYYVRL GSLSTKLHSR AYQQALSRVK      
       250        260        270        280        290        300   
EAKQKSQQTI SQLHSTVHLI EFARKNVYSA NQKIQDAQDK LYLSWVEWKR SIGYDDTDES     
       310        320        330        340        350        360   
HCAEHIESRT LAIARNLTQQ LQTTCHTLLS NIQGVPQNIQ DQAKHMGVMA GDIYSVFRNA    
       370        380        390        400        410        420   
ASFKEVSDSL LTSSKGQLQK MKESLDDVMD YLVNNTPLNW LVGPFYPQLT ESQNAQDQGA 
       430   
EMDKSSQETQ RSEHKTH 437  
Swiss-Prot entry Q99541; ADRP is the major lipid droplet protein. May be involved in development and maintenance of adipose tissue.
产品名称
目录号
规格
价格
Human Adipocyte Differentiation-Related Protein (ADRP)
00011-01-100
100 ug
询价
人脂肪细胞分化相关蛋白
00011-01-100
100 ug
询价

 

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Inhibition of ADRP prevents diet-induced insulin resistance

Diets with high fat content induce steatosis, insulin resistance and type 2 diabetes. The lipid droplet protein, Adipose Differentiation-Related Protein (ADRP), mediates hepatic steatosis but whether this affects insulin action in the liver or peripheral organs in diet-induced obesity is uncertain. We fed C57BL/6J mice a high-fat diet and simultaneously treated them with an antisense oligonucleotide (ASO) against ADRP for 4 weeks. Glucose homeostasis was assessed using clamp and tracer techniques. ADRP ASO decreased the levels of triglycerides and diacylglycerol in the liver, but fatty acids, long chain fatty acyl CoAs, ceramides and cholesterol were unchanged. Insulin action in the liver was enhanced following ADRP ASO treatment, whereas muscle and adipose tissue were not affected. ADRP ASO increased the phosphorylation IRS1, IRS2 and Akt, and decreased gluconeogenic enzymes and PKC{varepsilon}, consistent with its insulin sensitizing action. These results demonstrate an important role for ADRP in the pathogenesis of diet-induced insulin resistance.
Varela G.M. et al. Am J Physiol Gastrointest Liver Physiol (July 31, 2008). doi:10.1152/ajpgi.90204.2008
 
 
 

 

 


 
 
Adipokine Research