Abstract
We previously showed that a phosphate-deficient diet resulting in hypophosphatemia upregulated the catalytic subunit p36 of rat liver glucose-6-phosphatase, which is responsible for hepatic glucose production. A possible association between phosphate and glucose homeostasis was now further evaluated in the Hyp mouse, a murine homologue of human X-linked hypophosphatemia. We found that in the Hyp mouse as in the dietary Pi deficiency model, serum insulin was reduced while glycemia was increased, and that liver glucose-6-phosphatase activity was enhanced as a consequence of increased mRNA and protein levels of p36. In contrast, the Hyp model had decreased mRNA and protein levels of the putative glucose-6-phosphate translocase p46 and liver cyclic AMP was not increased as in the phosphate-deficient diet rats. It is concluded that in genetic as in dietary hypophosphatemia, elevated glucose-6-phosphatase activity could be partially responsible for the impaired glucose metabolism albeit through distinct mechanisms.
Key words
Glucose Intolerance - Phosphate Homeostasis - Mouse Liver
References
1
Foster J DF, Pederson B A, Nordlie R C.
Glucose-6-phosphatase structure, regulation, and function: an update.
Proc Soc Exp Biol Med.
1997;
215
314-332
2
Lei K J, Shelly L L, Pan C J, Sidbury J B, Chou J Y.
Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a.
Science.
1993;
262
580-583
3
Gerin I, Veiga-da-Cunha M, Achouri Y, Collet J F, van Schaftingen E.
Sequence of a putative glucose-6-phosphate translocase, mutation in glycogen storage disease type Ib.
FEBS Lett.
1997;
419
235-238
4
van de Werve G, Lange A, Newgard C, Méchin M C, Li Y, Berteloot A.
New lessons in the regulation of glucose metabolism taught by the glucose 6-phosphatase system.
Eur J Biochem.
2000;
267
1533-1549
5
Li Y, Méchin M C, van de Werve G.
Diabetes affects similarly the catalytic subunit and putative glucose-6-phosphate translocase of glucose-6-phosphatase.
J Biol Chem.
1999;
274
33 866-33 868
6
Li Y, van de Werve G.
Distinct hormone stimulation and counteraction by insulin of the expression of the two components of glucose 6-phosphatase in HepG2 cells.
Biochem Biophys Res Commun.
2000;
272
41-44
7
Trinh K Y, O’Doherty R M, Anderson P, Lange A J, Newgard C B.
Perturbation of fuel homeostasis caused by over-expression of the glucose-6-phosphatase catalytic subunit in liver of normal rats.
J Biol Chem.
1998;
273
31 615-31 620
8
Econs M J.
New insights into the pathogenesis of inherited phosphate wasting disorders.
Bone.
1999;
25
131-135
9
Lajeunesse D, Meyer Jr. R A, Hamel L.
Direct demonstration of a humorally-mediated inhibition of renal phosphate transport in the Hyp mouse.
Kidney Int.
1996;
50
1531-1538
10
The HYP Consortium .
A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets.
Nature Genet.
1995;
11
130-136
11
Du L, Desbarats M, Viel J, Glorieux F H, Cawthorn C, Ecarot B.
cDNA cloning of the murine Pex gene implicated in X-linked hypophosphatemia and evidence for expression in bone.
Genomics.
1996;
36
22-28
12
Guo R, Quarles L D.
Cloning and sequencing of human PEX from a bone cDNA library: evidence for its developmental stage-specific regulation in osteoblasts.
J Bone Miner Res.
1997;
12
1009-1017
13
DeFronzo R A, Lang R.
Hypophosphatemia and glucose intolerance: evidence for tissue insensitivity to insulin.
N Engl J Med.
1980;
303
1259-1263
14
Paula F J, Plens A E, Foss M C.
Effects of hypophosphatemia on glucose tolerance and insulin secretion.
Horm Metab Res.
1998;
30
281-284
15
Xie W S, Li Y, Méchin M C, van de Werve G.
Upregulation of liver glucose-6-phosphatase in rats fed with a Pi -deficient diet.
Biochem J.
1999;
343
393-396
16
Xie W S, Tran T L, Finegood D T, van de Werve G.
Dietary phosphate deprivation in rats affects liver cyclic AMP, glycogen, key steps of gluconeogenesis and glucose production.
Biochem J.
2000;
352
227-232
17
Méchin M C, Annabi B, Pegorier J P, van de Werve G.
Ontogeny of the catalytic subunit and putative glucose-6-phosphate transporter proteins of the rat microsomal liver glucose-6-phosphatase system.
Metabolism.
2000;
49
1200-1203
18
Tenenhouse H S.
X-linked hypophosphatemia: a homologous disorder in humans and mice.
Nephrol Dial Transplant.
1999;
14
333-341
19
Kido S, Miyamoto K, Mizobuchi H, Taketani Y, Ohkido I, Ogawa N, Kaneko Y, Harashima S, Takeda E.
Identification of regulatory sequences and binding proteins in the type II sodium/phosphate cotransporter NPT2 gene responsive to dietary phosphate.
J Biol Chem.
1999;
274
28 256-28 263
20
Cowgill L D, Goldfarb S, Lau K, Slatopolsky E.
Evidence for an intrinsic renal tubular defect in mice with genetic hypophosphatemic rickets.
J Clin Invest.
1979;
63
1203-1210
21
Kiebzak G M, Roos B A, Meyer Jr. R A.
Secondary hyperparathyroidism in X-linked hypophosphatemic mice.
Endocrinol.
1982;
111
650-652
22
Zhou X J, Fadda G Z, Perna A F, Massry S G.
Phosphate depletion impairs insulin secretion by pancreatic islets.
Kidney Int.
1991;
39
120-128
23
Moore E E, Kuestner R E, Conklin D C, Whitmore T E, Downey W, Buddle M M, Adams R L, Bell L A, Thompson D L, Wolf A, Chen L, Stamm M R, Grant F J, Lok S, Ren H, de Jongh K S.
Stanniocalcin 2: characterization of the protein and its localization to human pancreatic alpha cells.
Horm Metab Res.
1999;
31
406-414
24
Drezner M K.
PHEX gene and hypophosphatemia.
Kidney Int.
2000;
57
9-18
25
Shimada T, Mizutani S, Muto T, Vonega T, Hino R, Takeda S, Takeuchi Y, Fujita T, Fukumoto S, Yamashita T.
Cloning and characterization of FGF-23 as a causative factor of tumor-induced osteomalacia.
Proc Natl Acad Sci.
2001;
98
6500-6505
26
Bowe A E, Finnegan R, Jan de Beur S M, Cho J, Levine M A, Kumar R, Schiavi S C.
FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate.
Biochem Biophysical Res Comm.
2001;
284
977-981
27
Rowe P S, de Zoysa P A, Dong R, Wang H R, White K E, Econs M J, Oudet C L.
MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia.
Genomics.
2000;
67
54-68
28
Argiro L, Desbarats M, Glorieux F H, Ecarot B.
MEPE, the gene encoding a tumor-secreted protein in oncogenic hypophosphatemic osteomalacia, is expressed in bone.
Genomics.
2001;
74
342-351
G. van de Werve, Ph.D.
Département de Nutrition · Centre de Recherche du CHUM · Hôpital Notre-Dame ·
8ième Pavillon Malloux · 1560 rue Sherbrooke Est · Montréal · Québec H2L 4M1 · Canada ·
Fax: + 1 (514) 412 76 03
eMail: gerald_van_de_werve@hotmail.com