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Erschienen in: Acta Diabetologica 6/2014

01.12.2014 | Original Article

Glypican-4 is increased in human subjects with impaired glucose tolerance and decreased in patients with newly diagnosed type 2 diabetes

verfasst von: Ke Li, Xiaohui Xu, Wenjing Hu, Minyan Li, Mengliu Yang, Yaxu Wang, Yong Luo, Xianxiang Zhang, Hua Liu, Ling Li, Gangyi Yang

Erschienen in: Acta Diabetologica | Ausgabe 6/2014

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Abstract

Context

Glypican-4 (GPC-4) has been identified as a novel adipokine capable of enhancing insulin signaling. A significant association between circulating GPC-4 levels and nonalcoholic fatty liver disease and cardiometabolic risk factors has been found in women.

Objective

The aim of the present study was to investigate the relationship between GPC-4 and insulin resistance in cross-sectional and interventional studies.

Patients and design

We measured circulating GPC-4 (determined with ELISA) in subjects with NGT, IGT, and nT2DM. Euglycemic-hyperinsulinemic clamps were performed in healthy and T2DM subjects. Real-time RT-PCR and Western blotting were used to assess mRNA and protein expression of GPC-4.

Results

Circulating GPC-4 levels were significantly higher in IGT subjects and lower in nT2DM subjects compared to controls. Circulating GPC-4 was positively correlated with BMI, WHR, HOMA-IS, and FAT%, while it was inversely correlated with FBG and HbA1c. Excluding diabetic subjects, increasing GPC-4 levels were associated with HOMA-IR and M values. Significantly lower GPC-4 mRNA and protein levels were found in muscle and fat of nT2DM patients, compared to controls. GPC-4 levels were significantly increased upon an oral glucose intake. The secretion of GPC-4 exhibited a characteristic diurnal rhythm in humans, with a major rise occurring between afternoon and midnight.

Conclusions

Circulating GPC-4 is elevated in prediabetic subjects and is reduced in nT2DM patients. The elevated GPC-4 appears to be associated with insulin resistance and obesity in IGT subjects.
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Literatur
1.
Zurück zum Zitat Oda E (2012) Metabolic syndrome: its history, mechanisms, and limitations. Acta Diabetol 49:89–95PubMedCrossRef Oda E (2012) Metabolic syndrome: its history, mechanisms, and limitations. Acta Diabetol 49:89–95PubMedCrossRef
2.
Zurück zum Zitat Ying X, Qian Y, Jiang Y, Jiang Z, Song Z, Zhao C (2012) Association of the apolipoprotein B/apolipoprotein A-I ratio and low-density lipoprotein cholesterol with insulin resistance in a Chinese population with abdominal obesity. Acta Diabetol 49:465–472PubMedCrossRef Ying X, Qian Y, Jiang Y, Jiang Z, Song Z, Zhao C (2012) Association of the apolipoprotein B/apolipoprotein A-I ratio and low-density lipoprotein cholesterol with insulin resistance in a Chinese population with abdominal obesity. Acta Diabetol 49:465–472PubMedCrossRef
3.
Zurück zum Zitat Lili Z, Ling L, Mengliu Y, Hua L, Gangyi Y (2011) Elevated circulating vaspin levels were decreased by rosiglitazone therapy in T2DM patients with poor glycemic control on metformin alone. Cytokine 56:399–402CrossRef Lili Z, Ling L, Mengliu Y, Hua L, Gangyi Y (2011) Elevated circulating vaspin levels were decreased by rosiglitazone therapy in T2DM patients with poor glycemic control on metformin alone. Cytokine 56:399–402CrossRef
4.
Zurück zum Zitat Qin S, Ling L, Renzhe L, Mengliu Y, Hua L, Gangyi Y (2009) Overexpression of visfatin/pbef/nampt alters whole-body insulin sensitivity and lipid profile in rats. Ann Med 41:311–320CrossRef Qin S, Ling L, Renzhe L, Mengliu Y, Hua L, Gangyi Y (2009) Overexpression of visfatin/pbef/nampt alters whole-body insulin sensitivity and lipid profile in rats. Ann Med 41:311–320CrossRef
5.
Zurück zum Zitat Gangyi Y, Ling L, Wenwen C, Hua L, Boden G, Ke L (2009) Circulating preptin levels in normal, impaired glucose tolerance, and type 2 diabetic subjects. Ann Med 41:52–56CrossRef Gangyi Y, Ling L, Wenwen C, Hua L, Boden G, Ke L (2009) Circulating preptin levels in normal, impaired glucose tolerance, and type 2 diabetic subjects. Ann Med 41:52–56CrossRef
6.
Zurück zum Zitat Gesta S, Bluher M, Yamamoto Y, Norris AW, Berndt J, Kralisch S, Boucher J, Lewis C, Kahn CR (2006) Evidence for a role of developmental genes in the origin of obesity and body fat distribution. Proc Natl Acad Sci USA 103:6676–6681PubMedCentralPubMedCrossRef Gesta S, Bluher M, Yamamoto Y, Norris AW, Berndt J, Kralisch S, Boucher J, Lewis C, Kahn CR (2006) Evidence for a role of developmental genes in the origin of obesity and body fat distribution. Proc Natl Acad Sci USA 103:6676–6681PubMedCentralPubMedCrossRef
7.
Zurück zum Zitat Ussar S, Bezy O, Blüher M, Kahn CR (2012) Glypican-4 enhances insulin signaling via interaction with the insulin receptor and serves as a novel adipokine. Diabetes 61:2289–2298PubMedCentralPubMedCrossRef Ussar S, Bezy O, Blüher M, Kahn CR (2012) Glypican-4 enhances insulin signaling via interaction with the insulin receptor and serves as a novel adipokine. Diabetes 61:2289–2298PubMedCentralPubMedCrossRef
8.
Zurück zum Zitat Yoo HJ, Hwang SY, Cho GJ, Hong HC, Choi HY, Hwang TG, Kim SM, Blüher M, Youn BS, Baik SH, Choi KM (2013) Association of glypican-4 with body fat distribution, insulin resistance, and nonalcoholic Fatty liver disease. J Clin Endocrinol Metab 98:2897–2901PubMedCrossRef Yoo HJ, Hwang SY, Cho GJ, Hong HC, Choi HY, Hwang TG, Kim SM, Blüher M, Youn BS, Baik SH, Choi KM (2013) Association of glypican-4 with body fat distribution, insulin resistance, and nonalcoholic Fatty liver disease. J Clin Endocrinol Metab 98:2897–2901PubMedCrossRef
9.
Zurück zum Zitat Alberti KG, Zimmet PZ (1998) Definition, diagnosis and classification of diabetes mellitus and its complications. 1. Diagnosis and classification of diabetes mellitus, provisional report of a WHO consultation. Diabet Med 15:539–553PubMedCrossRef Alberti KG, Zimmet PZ (1998) Definition, diagnosis and classification of diabetes mellitus and its complications. 1. Diagnosis and classification of diabetes mellitus, provisional report of a WHO consultation. Diabet Med 15:539–553PubMedCrossRef
10.
Zurück zum Zitat Mengliu Y, Rui L, Su L, Lili Z, Dongfang L, Yaxu W, Zhengai X, Boden G, Shirong C, Ling L, Gangyi Y (2013) Zinc-α2-glycoprotein is associated with insulin resistance in humans and is regulated by hyperglycemia, hyperinsulinemia or liraglutide administration: cross-sectional and interventional studies in normal, insulin-resistant, and newly diagnosed diabetic subjects. Diabetes Care 36:1074–1082CrossRef Mengliu Y, Rui L, Su L, Lili Z, Dongfang L, Yaxu W, Zhengai X, Boden G, Shirong C, Ling L, Gangyi Y (2013) Zinc-α2-glycoprotein is associated with insulin resistance in humans and is regulated by hyperglycemia, hyperinsulinemia or liraglutide administration: cross-sectional and interventional studies in normal, insulin-resistant, and newly diagnosed diabetic subjects. Diabetes Care 36:1074–1082CrossRef
11.
Zurück zum Zitat Wenjing H, Ling L, Mengliu Y, Xiaohe L, Wenxia R, Dongfang L, Zhengai X, Hua L, Gangyi Y (2013) Circulating Sfrp5 is a signature of obesity-related metabolic disorders and is regulated by glucose and liraglutide in humans. J Clin Endocrinol Metab 98:290–298CrossRef Wenjing H, Ling L, Mengliu Y, Xiaohe L, Wenxia R, Dongfang L, Zhengai X, Hua L, Gangyi Y (2013) Circulating Sfrp5 is a signature of obesity-related metabolic disorders and is regulated by glucose and liraglutide in humans. J Clin Endocrinol Metab 98:290–298CrossRef
12.
Zurück zum Zitat AlbaredaM Rodnguez-Espinosa J, Murugo M, de Leiva A, Corcoy R (2000) Assessment of insulin sensitivity and beta-cell function from measurements in the fasting state and during an oral glucose tolerance test. Diabetologia 43:1507–1511CrossRef AlbaredaM Rodnguez-Espinosa J, Murugo M, de Leiva A, Corcoy R (2000) Assessment of insulin sensitivity and beta-cell function from measurements in the fasting state and during an oral glucose tolerance test. Diabetologia 43:1507–1511CrossRef
14.
Zurück zum Zitat Sinha MK, Ohannesian JP, Heiman ML, Kriauciunas A, Stephens TW, Magosin S (1996) Nocturnal rise of leptin in lean, obese, and non-insulin dependent diabetes mellitus subjects. J Clin Invest 97:1344–1347PubMedCentralPubMedCrossRef Sinha MK, Ohannesian JP, Heiman ML, Kriauciunas A, Stephens TW, Magosin S (1996) Nocturnal rise of leptin in lean, obese, and non-insulin dependent diabetes mellitus subjects. J Clin Invest 97:1344–1347PubMedCentralPubMedCrossRef
15.
Zurück zum Zitat Traister A, Shi W, Filmus J (2007) Mammalian Notum induces the release of glypicans and other GPI-anchored proteins from the cell surface. Biochem J 410:503–511CrossRef Traister A, Shi W, Filmus J (2007) Mammalian Notum induces the release of glypicans and other GPI-anchored proteins from the cell surface. Biochem J 410:503–511CrossRef
16.
Zurück zum Zitat Brunner G, Metz CN, Nguyen H, Gabrilove J, Patel SR, Davitz MA, Rifkin DB, Wilson EL (1994) An endogenous glycosylphosphatidylinositol-specific phospholipase D releases basic fibroblast growth factor-heparan sulfate proteoglycan complexes from human bone marrow cultures. Blood 83:2115–2125PubMed Brunner G, Metz CN, Nguyen H, Gabrilove J, Patel SR, Davitz MA, Rifkin DB, Wilson EL (1994) An endogenous glycosylphosphatidylinositol-specific phospholipase D releases basic fibroblast growth factor-heparan sulfate proteoglycan complexes from human bone marrow cultures. Blood 83:2115–2125PubMed
17.
Zurück zum Zitat Raikwar NS, Bowen-Deeg RF, Du XS, Low MG, Deeg MA (2010) Glycosylphosphatidylinositol-specific phospholipase D improves glucose tolerance. Metabolism 59:1413–1420PubMedCrossRef Raikwar NS, Bowen-Deeg RF, Du XS, Low MG, Deeg MA (2010) Glycosylphosphatidylinositol-specific phospholipase D improves glucose tolerance. Metabolism 59:1413–1420PubMedCrossRef
18.
Zurück zum Zitat Saltiel AR, Cuatrecasas P (1988) In search of a second messenger for insulin. Am J Physiol 255:C1–C11PubMed Saltiel AR, Cuatrecasas P (1988) In search of a second messenger for insulin. Am J Physiol 255:C1–C11PubMed
19.
Zurück zum Zitat Bowen RF, Raikwar NS, Olson LK, Deeg MA (2001) Glucose and insulin regulate glycosylphosphatidylinositol-specific phospholipase D expression in islet beta cells. Metabolism 50:1489–1492PubMedCrossRef Bowen RF, Raikwar NS, Olson LK, Deeg MA (2001) Glucose and insulin regulate glycosylphosphatidylinositol-specific phospholipase D expression in islet beta cells. Metabolism 50:1489–1492PubMedCrossRef
Metadaten
Titel
Glypican-4 is increased in human subjects with impaired glucose tolerance and decreased in patients with newly diagnosed type 2 diabetes
verfasst von
Ke Li
Xiaohui Xu
Wenjing Hu
Minyan Li
Mengliu Yang
Yaxu Wang
Yong Luo
Xianxiang Zhang
Hua Liu
Ling Li
Gangyi Yang
Publikationsdatum
01.12.2014
Verlag
Springer Milan
Erschienen in
Acta Diabetologica / Ausgabe 6/2014
Print ISSN: 0940-5429
Elektronische ISSN: 1432-5233
DOI
https://doi.org/10.1007/s00592-014-0652-5

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