Lake Andrew C, Sun Ying, Li Jian-Liang, Kim Jae Eun, Johnson Jeremy W, Li Dongmei, Revett Tracy, Shih Heather H, Liu Wei, Paulsen Janet E, Gimeno Ruth E
Biological Technologies, Wyeth Research, Cambridge, MA 02140, USA.
J Lipid Res. 2005 Nov;46(11):2477-87. doi: 10.1194/jlr.M500290-JLR200. Epub 2005 Sep 8.
Adiponutrin and a related protein, adipocyte triglyceride lipase (ATGL; also known as Desnutrin), were recently described as adipocyte-specific proteins with lipid hydrolase activity. Using bioinformatics, we identified three additional Adiponutrin family members (GS2, GS2-Like, and PNPLA1). Here, we report on the expression, regulation, and activity of GS2 and GS2-Like compared with Adiponutrin and Desnutrin/ATGL. GS2-Like is expressed and regulated in a manner similar to Adiponutrin; however, the absolute levels of mRNA are significantly lower than those of Adiponutrin or Desnutrin/ATGL. GS2 transcripts were identified only in humans and are highly expressed in adipose as well as other tissues. All four proteins show lipase activity in vitro, which is dependent on the presence of the active site serine for Adiponutrin, Desnutrin/ATGL, and GS2. Overexpression of Desnutrin/ATGL, GS2, and GS2-Like, but not Adiponutrin, decreases intracellular triglyceride levels. This is consistent with a function for Desnutrin/ATGL, GS2, and GS2-Like in lipolysis, but not for Adiponutrin. Consistent with previously reported data, Desnutrin/ATGL is upregulated by fasting in adipose tissue, whereas Adiponutrin is downregulated. Additionally, Adiponutrin and GS2-Like, but not Desnutrin/ATGL, are strongly induced in the liver of ob/ob mice. Our data support distinct functions for Adiponutrin and Desnutrin/ATGL and raise the possibility that GS2 may contribute significantly to lipolysis in human adipose tissue.
脂肪营养蛋白和一种相关蛋白,即脂肪细胞甘油三酯脂肪酶(ATGL;也称为去营养蛋白),最近被描述为具有脂质水解酶活性的脂肪细胞特异性蛋白。通过生物信息学,我们鉴定出另外三个脂肪营养蛋白家族成员(GS2、GS2样蛋白和PNPLA1)。在此,我们报告了GS2和GS2样蛋白与脂肪营养蛋白和去营养蛋白/ATGL相比的表达、调控及活性。GS2样蛋白的表达和调控方式与脂肪营养蛋白相似;然而,其mRNA的绝对水平显著低于脂肪营养蛋白或去营养蛋白/ATGL。GS2转录本仅在人类中被鉴定出,且在脂肪组织以及其他组织中高表达。所有这四种蛋白在体外均表现出脂肪酶活性,这对于脂肪营养蛋白、去营养蛋白/ATGL和GS2而言依赖于活性位点丝氨酸的存在。去营养蛋白/ATGL、GS2和GS2样蛋白(而非脂肪营养蛋白)的过表达降低细胞内甘油三酯水平。这与去营养蛋白/ATGL、GS2和GS2样蛋白在脂肪分解中的作用一致,而与脂肪营养蛋白的作用不一致。与先前报道的数据一致,去营养蛋白/ATGL在脂肪组织中因禁食而上调,而脂肪营养蛋白则下调。此外,脂肪营养蛋白和GS2样蛋白(而非去营养蛋白/ATGL)在ob/ob小鼠的肝脏中被强烈诱导。我们的数据支持脂肪营养蛋白和去营养蛋白/ATGL具有不同功能,并提出GS2可能对人类脂肪组织中的脂肪分解有显著贡献的可能性。