Other
21 Authors
- Chen W,
- Harris TE,
- Pagac M,
- Kotevski D,
- Huang X,
- Yang H,
- Parton RG,
- Lukmantara IE,
- Sadowski P,
- Liu Z,
- Lei M,
- Qi Y,
- Tian Y,
- Boroda S,
- Cooper DE,
- Wu Z,
- Liu G,
- Coleman RA,
- Ferguson C,
- Mak HY,
- Du X
| First Author | Pagac M | Year | 2016 |
| Journal | Cell Rep | Volume | 17 |
| Issue | 6 | Pages | 1546-1559 |
| PubMed ID | 27806294 | Mgi Jnum | J:242338 |
| Mgi Id | MGI:5904930 | Doi | 10.1016/j.celrep.2016.10.037 |
| Citation | Pagac M, et al. (2016) SEIPIN Regulates Lipid Droplet Expansion and Adipocyte Development by Modulating the Activity of Glycerol-3-phosphate Acyltransferase. Cell Rep 17(6):1546-1559 |
| abstractText | Berardinelli-Seip congenital lipodystrophy 2 (BSCL2) is caused by loss-of-function mutations in SEIPIN, a protein implicated in both adipogenesis and lipid droplet expansion but whose molecular function remains obscure. Here, we identify physical and functional interactions between SEIPIN and microsomal isoforms of glycerol-3-phosphate acyltransferase (GPAT) in multiple organisms. Compared to controls, GPAT activity was elevated in SEIPIN-deficient cells and tissues and GPAT kinetic values were altered. Increased GPAT activity appears to underpin the block in adipogenesis and abnormal lipid droplet morphology associated with SEIPIN loss. Overexpression of Gpat3 blocked adipogenesis, and Gpat3 knockdown in SEIPIN-deficient preadipocytes partially restored differentiation. GPAT overexpression in yeast, preadipocytes, and fly salivary glands also formed supersized lipid droplets. Finally, pharmacological inhibition of GPAT in Seipin-/- mouse preadipocytes partially restored adipogenesis. These data identify SEIPIN as an evolutionarily conserved regulator of microsomal GPAT and suggest that GPAT inhibitors might be useful for the treatment of human BSCL2 patients. |
