Aquaporin Adipose, a Putative Glycerol Channel in Adipocytes*

Adipose tissue is a major site of glycerol production in response to energy balance. However, molecular basis of glycerol release from adipocytes has not yet been elucidated. We recently cloned a novel member of the aquaporin family, aquaporin adipose (AQPap), which has glycerol permeability. The current study was designed to examine the hypothesis that AQPap serves as a glycerol channel in adipocytes. Adipose tissue expressed AQPap mRNA in high abundance, but not the mRNAs for the other aquaglyceroporins, AQP3 and AQP9, indicating that AQPap is the only known aquaglyceroporin expressed in adipose tissue. Glycerol release from 3T3-L1 cells was increased during differentiation in parallel with AQPap mRNA levels and suppressed by mercury ion, which inhibits the function of AQPs, supporting AQPap functions as a glycerol channel in adipocytes. Fasting increased and refeeding suppressed adipose AQPap mRNA levels in accordance with plasma glycerol levels and oppositely to plasma insulin levels in mice. Insulin dose-dependently suppressed AQPap mRNA expression in 3T3-L1 cells. AQPap mRNA levels and adipose glycerol concentrations measured by the microdialysis technique were increased in obese mice with insulin resistance. Accordingly, negative regulation of AQPap expression by insulin was impaired in the insulin-resistant state. Exposure of epinephrine translocated AQPap protein from perinuclear cytoplasm to the plasma membrane in 3T3-L1 adipocytes. These results strongly suggest that AQPap plays an important role in glycerol release from adipocytes.

[1]  A. Green,et al.  Long-term regulation of lipolysis and hormone-sensitive lipase by insulin and glucose. , 1999, Diabetes.

[2]  M. Hediger,et al.  Molecular Characterization of a Broad Selectivity Neutral Solute Channel* , 1998, The Journal of Biological Chemistry.

[3]  J. Peters,et al.  Expression of Putative Fatty Acid Transporter Genes Are Regulated by Peroxisome Proliferator-activated Receptor α and γ Activators in a Tissue- and Inducer-specific Manner* , 1998, The Journal of Biological Chemistry.

[4]  D. Thomas,et al.  Prediction of functional residues in water channels and related proteins , 1998, Protein science : a publication of the Protein Society.

[5]  C. Wernstedt,et al.  Identification of Novel Phosphorylation Sites in Hormone-sensitive Lipase That Are Phosphorylated in Response to Isoproterenol and Govern Activation Properties in Vitro * , 1998, The Journal of Biological Chemistry.

[6]  Y. Matsuzawa,et al.  Molecular cloning and expression of a novel human aquaporin from adipose tissue with glycerol permeability. , 1997, Biochemical and biophysical research communications.

[7]  Tadashi Yamamoto,et al.  Molecular Cloning of a New Aquaporin from Rat Pancreas and Liver* , 1997, The Journal of Biological Chemistry.

[8]  F. Marumo,et al.  Cloning and functional expression of a second new aquaporin abundantly expressed in testis. , 1997, Biochemical and biophysical research communications.

[9]  F. Marumo,et al.  Cloning and Functional Expression of a New Water Channel Abundantly Expressed in the Testis Permeable to Water, Glycerol, and Urea* , 1997, The Journal of Biological Chemistry.

[10]  R. O’Brien,et al.  Regulation of gene expression by insulin. , 1996, The Biochemical journal.

[11]  S. Yamashita,et al.  Enhanced expression of PAI–1 in visceral fat: Possible contributor to vascular disease in obeisty , 1996, Nature Medicine.

[12]  P. Grimaldi,et al.  Expression of the CD36 homolog (FAT) in fibroblast cells: effects on fatty acid transport. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[13]  F. Marumo,et al.  cAMP-dependent Phosphorylation Stimulates Water Permeability of Aquaporin-collecting Duct Water Channel Protein Expressed in Xenopus Oocytes(*) , 1995, The Journal of Biological Chemistry.

[14]  R. Wolfe,et al.  Glycerol gluconeogenesis in fasting humans. , 1995, Nutrition.

[15]  S. Nielsen,et al.  Vasopressin increases water permeability of kidney collecting duct by inducing translocation of aquaporin-CD water channels to plasma membrane. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[16]  P. Agre,et al.  Molecular Cloning and Characterization of an Aquaporin cDNA from Salivary, Lacrimal, and Respiratory Tissues (*) , 1995, The Journal of Biological Chemistry.

[17]  J. Baraban,et al.  Molecular characterization of an aquaporin cDNA from brain: candidate osmoreceptor and regulator of water balance. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[18]  E. Windhager,et al.  Cloning and expression of AQP3, a water channel from the medullary collecting duct of rat kidney. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[19]  H. Lodish,et al.  Expression cloning and characterization of a novel adipocyte long chain fatty acid transport protein , 1994, Cell.

[20]  P. Kern,et al.  Hormonal regulation of hormone-sensitive lipase activity and mRNA levels in isolated rat adipocytes. , 1994, Journal of lipid research.

[21]  M. Knepper The aquaporin family of molecular water channels. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[22]  T. Gojobori,et al.  Molecular cloning and expression of a member of the aquaporin family with permeability to glycerol and urea in addition to water expressed at the basolateral membrane of kidney collecting duct cells. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[23]  B. V. van Oost,et al.  Requirement of human renal water channel aquaporin-2 for vasopressin-dependent concentration of urine. , 1994, Science.

[24]  A. Kimmel,et al.  Isolation of cDNAs for perilipins A and B: sequence and expression of lipid droplet-associated proteins of adipocytes. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[25]  A. Verkman,et al.  Cloning of a novel rat kidney cDNA homologous to CHIP28 and WCH-CD water channels. , 1993, Biochemical and biophysical research communications.

[26]  Y. Hirata,et al.  Cloning and expression of apical membrane water channel of rat kidney collecting tubule , 1993, Nature.

[27]  P. Agre,et al.  The mercury-sensitive residue at cysteine 189 in the CHIP28 water channel. , 1993, The Journal of biological chemistry.

[28]  A. Verkman,et al.  Functional reconstitution of the isolated erythrocyte water channel CHIP28. , 1992, The Journal of biological chemistry.

[29]  P. Jansson,et al.  Glycerol production in subcutaneous adipose tissue in lean and obese humans. , 1992, The Journal of clinical investigation.

[30]  P. Arner,et al.  Microdialysis of adipose tissue , 1991, Journal of internal medicine.

[31]  A. Greenberg,et al.  Perilipin, a major hormonally regulated adipocyte-specific phosphoprotein associated with the periphery of lipid storage droplets. , 1991, The Journal of biological chemistry.

[32]  G. Kimmich,et al.  Low-affinity intestinal L-aspartate transport with 2:1 coupling stoichiometry for Na+/Asp. , 1988, The American journal of physiology.

[33]  M. Kasuga,et al.  Studies with antipeptide antibody suggest the presence of at least two types of glucose transporter in rat brain and adipocyte. , 1988, The Journal of biological chemistry.

[34]  G. Dhillon,et al.  cAMP-dependent protein kinase and lipolysis in rat adipocytes. II. Definition of steady-state relationship with lipolytic and antilipolytic modulators. , 1985, The Journal of biological chemistry.

[35]  J. Revel,et al.  The major intrinsic protein (MIP) of the bovine lens fiber membrane: Characterization and structure based on cDNA cloning , 1984, Cell.

[36]  G. Guilbault,et al.  Fluorometric and colorimetric enzymic determination of triglycerides (triacylglycerols) in serum. , 1980, Clinical chemistry.

[37]  O. Rosen,et al.  Development of hormone receptors and hormonal responsiveness in vitro. Insulin receptors and insulin sensitivity in the preadipocyte and adipocyte forms of 3T3-L1 cells. , 1978, The Journal of biological chemistry.

[38]  S. Kihara,et al.  Troglitazone enhances glucose uptake and inhibits mitogen-activated protein kinase in human aortic smooth muscle cells. , 1998, Atherosclerosis.

[39]  R. Bergman,et al.  Central Role of the Adipocyte in Insulin Resistance , 1998, Journal of basic and clinical physiology and pharmacology.

[40]  D. Janero,et al.  Hydroperoxide-induced oxidative stress impairs heart muscle cell carbohydrate metabolism. , 1994, The American journal of physiology.

[41]  Y. Yazaki,et al.  Expression of glucose transporter isoforms with aging. , 1992, Gerontology.

[42]  A. Consoli,et al.  Increased lipolysis and its consequences on gluconeogenesis in non-insulin-dependent diabetes mellitus. , 1992, The Journal of clinical investigation.

[43]  P. Spooner,et al.  Effect of epinephrine and other lipolytic agents on intracellular lipolysis and lipoprotein lipase activity in 3T3-L1 adipocytes. , 1986, Journal of lipid research.

[44]  W. Stremmel,et al.  Isolation and partial characterization of a fatty acid binding protein in rat liver plasma membranes. , 1985, Proceedings of the National Academy of Sciences of the United States of America.