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Inputs and outputs of insulin receptor

  • Yipeng Du ,
  • Taotao Wei
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  • National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China

Received date: 28 Dec 2013

Accepted date: 26 Jan 2014

Published date: 23 Jun 2014

Copyright

2014 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

The insulin receptor (IR) is an important hub in insulin signaling and its activation is tightly regulated. Upon insulin stimulation, IR is activated through autophosphorylation, and consequently phosphorylates several insulin receptor substrate (IRS) proteins, including IRS1-6, Shc and Gab1. Certain adipokines have also been found to activate IR. On the contrary, PTP, Grb and SOCS proteins, which are responsible for the negative regulation of IR, are characterized as IR inhibitors. Additionally, many other proteins have been identified as IR substrates and participate in the insulin signaling pathway. To provide a more comprehensive understanding of the signals mediated through IR, we reviewed the upstream and downstream signal molecules of IR, summarized the positive and negative modulators of IR, and discussed the IR substrates and interacting adaptor proteins. We propose that the molecular events associated with IR should be integrated to obtain a better understanding of the insulin signaling pathway and diabetes.

Cite this article

Yipeng Du , Taotao Wei . Inputs and outputs of insulin receptor[J]. Protein & Cell, 2014 , 5(3) : 203 -213 . DOI: 10.1007/s13238-014-0030-7

1
Adeghate E (2008) Visfatin: structure, function and relation to diabetes mellitus and other dysfunctions. Curr Med Chem15: 1851-1862

DOI

2
Ahmad F, Goldstein BJ (1997) Functional association between the insulin receptor and the transmembrane protein-tyrosine phosphatase LAR in intact cells. J Biol Chem272: 448-457

DOI

3
Ahmed Z, Smith BJ, Pillay TS (2000) The APS adapter protein couples the insulin receptor to the phosphorylation of c-Cbl and facilitates ligand-stimulated ubiquitination of the insulin receptor. FEBS Lett475: 31-34

DOI

4
Alonso A, Sasin J, Bottini N, Friedberg I, Friedberg I, Osterman A, Godzik A, Hunter T, Dixon J, Mustelin T (2004) Protein tyrosine phosphatases in the human genome. Cell117: 699-711

DOI

5
Andersen JN, Mortensen OH, Peters GH, Drake PG, Iversen LF, Olsen OH, Jansen PG, Andersen HS, Tonks NK, Moller NP (2001) Structural and evolutionary relationships among protein tyrosine phosphatase domains. Mol Cell Biol21: 7117-7136

DOI

6
Andersen JN, Jansen PG, Echwald SM, Mortensen OH, Fukada T, Del Vecchio R, Tonks NK, Moller NP (2004) A genomic perspective on protein tyrosine phosphatases: gene structure, pseudogenes, and genetic disease linkage. FASEB J18: 8-30

DOI

7
Auberger P, Falquerho L, Contreres JO, Pages G, Le Cam G, Rossi B, Le Cam A (1989) Characterization of a natural inhibitor of the insulin receptor tyrosine kinase: cDNA cloning, purification, and anti-mitogenic activity. Cell58: 631-640

DOI

8
Baltensperger K, Karoor V, Paul H, Ruoho A, Czech MP, Malbon CC (1996) The beta-adrenergic receptor is a substrate for the insulin receptor tyrosine kinase. J Biol Chem271: 1061-1064

DOI

9
Baron V, Calleja V, Ferrari P, Alengrin F, Van Obberghen E (1998) p125Fak focal adhesion kinase is a substrate for the insulin and insulin-like growth factor-I tyrosine kinase receptors. J Biol Chem273: 7162-7168

DOI

10
Benaim G, Villalobo A (2002) Phosphorylation of calmodulin. Functional implications. Eur J Biochem269: 3619-3631

DOI

11
Bollag GE, Roth RA, Beaudoin J, Mochly-Rosen D, Koshland DE Jr (1986) Protein kinase C directly phosphorylates the insulin receptor in vitro and reduces its protein-tyrosine kinase activity. Proc Natl Acad Sci USA83: 5822-5824

DOI

12
Boucher J, Quilliot D, Praderes JP, Simon MF, Gres S, Guigne C, Prevot D, Ferry G, Boutin JA, Carpene C (2005) Potential involvement of adipocyte insulin resistance in obesity-associated up-regulation of adipocyte lysophospholipase D/autotaxin expression. Diabetologia48: 569-577

DOI

13
Braiman L, Alt A, Kuroki T, Ohba M, Bak A, Tennenbaum T, Sampson SR (2001) Insulin induces specific interaction between insulin receptor and protein kinase C delta in primary cultured skeletal muscle. Mol Endocrinol15: 565-574

DOI

14
Buelt MK, Shekels LL, Jarvis BW, Bernlohr DA (1991) In vitro phosphorylation of the adipocyte lipid-binding protein (p15) by the insulin receptor. Effects of fatty acid on receptor kinase and substrate phosphorylation. J Biol Chem266: 12266-12271

15
Cai D, Dhe-Paganon S, Melendez PA, Lee J, Shoelson SE (2003) Two new substrates in insulin signaling, IRS5/DOK4 and IRS6/ DOK5. J Biol Chem278: 25323-25330

DOI

16
Chen J, Sadowski HB, Kohanski RA, Wang LH (1997) Stat5 is a physiological substrate of the insulin receptor. Proc Natl Acad Sci USA94: 2295-2300

DOI

17
Costanzo BV, Trischitta V, Di Paola R, Spampinato D, Pizzuti A, Vigneri R, Frittitta L (2001) The Q allele variant (GLN121) of membrane glycoprotein PC-1 interacts with the insulin receptor and inhibits insulin signaling more effectively than the common K allele variant (LYS121). Diabetes50: 831-836

DOI

18
Dadke S, Kusari A, Kusari J (2001) Phosphorylation and activation of protein tyrosine phosphatase (PTP) 1B by insulin receptor. Mol Cell Biochem221: 147-154

DOI

19
Delahaye L, Rocchi S, Van Obberghen E (2000) Potential involvement of FRS2 in insulin signaling. Endocrinology141: 621-628

DOI

20
Delibegovic M, Bence KK, Mody N, Hong EG, Ko HJ, Kim JK, Kahn BB, Neel BG (2007) Improved glucose homeostasis in mice with muscle-specific deletion of protein-tyrosine phosphatase 1B. Mol Cell Biol27: 7727-7734

DOI

21
Delibegovic M, Zimmer D, Kauffman C, Rak K, Hong EG, Cho YR, Kim JK, Kahn BB, Neel BG, Bence KK (2009) Liver-specific deletion of protein-tyrosine phosphatase 1B (PTP1B) improves metabolic syndrome and attenuates diet-induced endoplasmic reticulum stress. Diabetes58: 590-599

DOI

22
Di Cristofano A, Carpino N, Dunant N, Friedland G, Kobayashi R, Strife A, Wisniewski D, Clarkson B, Pandolfi PP, Resh MD (1998) Molecular cloning and characterization of p56dok-2 defines a new family of RasGAP-binding proteins. J Biol Chem273: 4827-4830

DOI

23
Dubois MJ, Bergeron S, Kim HJ, Dombrowski L, Perreault M, Fournes B, Faure R, Olivier M, Beauchemin N, Shulman GI (2006) The SHP-1 protein tyrosine phosphatase negatively modulates glucose homeostasis. Nat Med12: 549-556

DOI

24
Emanuelli B, Peraldi P, Filloux C, Sawka-Verhelle D, Hilton D, Van Obberghen E (2000) SOCS-3 is an insulin-induced negative regulator of insulin signaling. J Biol Chem275: 15985-15991

DOI

25
Fantin VR, Sparling JD, Slot JW, Keller SR, Lienhard GE, Lavan BE (1998) Characterization of insulin receptor substrate 4 in human embryonic kidney 293 cells. J Biol Chem273: 10726-10732

DOI

26
Formisano P, Najjar SM, Gross CN, Philippe N, Oriente F, Kern-Buell CL, Accili D, Gorden P (1995) Receptor-mediated internalization of insulin. Potential role of pp120/HA4, a substrate of the insulin receptor kinase. J Biol Chem270: 24073-24077

27
Galic S, Klingler-Hoffmann M, Fodero-Tavoletti MT, Puryer MA, Meng TC, Tonks NK, Tiganis T (2003) Regulation of insulin receptor signaling by the protein tyrosine phosphatase TCPTP. Mol Cell Biol23: 2096-2108

DOI

28
Galic S, Hauser C, Kahn BB, Haj FG, Neel BG, Tonks NK, Tiganis T (2005) Coordinated regulation of insulin signaling by the protein tyrosine phosphatases PTP1B and TCPTP. MolCell Biol25: 819-829

DOI

29
Goustin AS, Abou-Samra AB (2011) The “thrifty” gene encoding Ahsg/Fetuin-A meets the insulin receptor: Insights into the mechanism of insulin resistance. Cell Signal23: 980-990

DOI

30
Griffin ME, Marcucci MJ, Cline GW, Bell K, Barucci N, Lee D, Goodyear LJ, Kraegen EW, White MF, Shulman GI (1999) Free fatty acid-induced insulin resistance is associated with activation of protein kinase C theta and alterations in the insulin signaling cascade. Diabetes48: 1270-1274

DOI

31
Grupe A, Alleman J, Goldfine ID, Sadick M, Stewart TA (1995) Inhibition of insulin receptor phosphorylation by PC-1 is not mediated by the hydrolysis of adenosine triphosphate or the generation of adenosine. J Biol Chem270: 22085-22088

DOI

32
Gual P, Baron V, Lequoy V, Van Obberghen E (1998) Interaction of Janus kinases JAK-1 and JAK-2 with the insulin receptor and the insulin-like growth factor-1 receptor. Endocrinology139: 884-893

DOI

33
Hanke S, Mann M (2009) The phosphotyrosine interactome of the insulin receptor family and its substrates IRS-1 and IRS-2. Mol Cell Proteomics8: 519-534

DOI

34
Hansen H, Svensson U, Zhu J, Laviola L, Giorgino F, Wolf G, Smith RJ, Riedel H (1996) Interaction between the Grb10 SH2 domain and the insulin receptor carboxyl terminus. J Biol Chem271: 8882-8886

DOI

35
Hashimoto N, Feener EP, Zhang WR, Goldstein BJ (1992) Insulin receptor protein-tyrosine phosphatases. Leukocyte common antigen-related phosphatase rapidly deactivates the insulin receptor kinase by preferential dephosphorylation of the receptor regulatory domain. J Biol Chem267: 13811-13814

36
Hayashi H, Nishioka Y, Kamohara S, Kanai F, Ishii K, Fukui Y, Shibasaki F, Takenawa T, Kido H, Katsunuma N (1993) The alpha-type 85-kDa subunit of phosphatidylinositol 3-kinase is phosphorylated at tyrosines 368, 580, and 607 by the insulin receptor. J Biol Chem268: 7107-7117

37
Holt LJ, Siddle K (2005) Grb10 and Grb14: enigmatic regulators of insulin action-and more? Biochem J388: 393-406

DOI

38
Hotamisligil GS, Johnson RS, Distel RJ, Ellis R, Papaioannou VE, Spiegelman BM (1996) Uncoupling of obesity from insulin resistance through a targeted mutation in aP2, the adipocyte fatty acid binding protein. Science274: 1377-1379

DOI

39
Hresko RC, Mueckler M (2000) A novel 68-kDa adipocyte protein phosphorylated on tyrosine in response to insulin and osmotic shock. J Biol Chem275: 18114-18120

DOI

40
Hresko RC, Mueckler M (2002) Identification of pp68 as the tyrosinephosphorylated form of SYNCRIP/NSAP1. A cytoplasmic RNAbinding protein. J Biol Chem277: 25233-25238

DOI

41
Itani SI, Zhou Q, Pories WJ, MacDonald KG, Dohm GL (2000) Involvement of protein kinase C in human skeletal muscle insulin resistance and obesity. Diabetes49: 1353-1358

DOI

42
Jornayvaz FR, Shulman GI (2012) Diacylglycerol activation of protein kinase Cepsilon and hepatic insulin resistance. Cell Metab15: 574-584

DOI

43
Jornayvaz FR, Birkenfeld AL, Jurczak MJ, Kanda S, Guigni BA, Jiang DC, Zhang D, Lee HY, Samuel VT, Shulman GI (2011) Hepatic insulin resistance inmicewith hepatic overexpression of diacylglycerol acyltransferase 2. Proc Natl Acad Sci USA108: 5748-5752

DOI

44
Joyal JL, Crimmins DL, Thoma RS, Sacks DB (1996) Identification of insulin-stimulated phosphorylation sites on calmodulin. Biochemistry35: 6267-6275

DOI

45
Kalabay L, Cseh K, Pajor A, Baranyi E, Csakany GM, Melczer Z, Speer G, Kovacs M, Siller G, Karadi I (2002) Correlation of maternal serum fetuin/alpha2-HS-glycoprotein concentration with maternal insulin resistance and anthropometric parameters of neonates in normal pregnancy and gestational diabetes. Eur J Endocrinol147: 243-248

DOI

46
Karoor V, Wang L, Wang HY, Malbon CC (1998) Insulin stimulates sequestration of beta-adrenergic receptors and enhanced association of beta-adrenergic receptors with Grb2 via tyrosine 350. J Biol Chem273: 33035-33041

DOI

47
Kasus-Jacobi A, Bereziat V, Perdereau D, Girard J, Burnol AF (2000) Evidence for an interaction between the insulin receptor and Grb7. A role for two of its binding domains, PIR and SH2. Oncogene19: 2052-2059

DOI

48
Kato K, Nishimasu H, Okudaira S, Mihara E, Ishitani R, Takagi J, Aoki J, Nureki O (2012) Crystal structure of Enpp1, an extracellular glycoprotein involved in bone mineralization and insulin signaling. Proc Natl Acad Sci USA109: 16876-16881

DOI

49
Kharitonenkov A, Schnekenburger J, Chen Z, Knyazev P, Ali S, Zwick E, White M, Ullrich A (1995) Adapter function of proteintyrosine phosphatase 1D in insulin receptor/insulin receptor substrate-1 interaction. J Biol Chem270: 29189-29193

DOI

50
Kong M, Wang CS, Donoghue DJ (2002) Interaction of fibroblast growth factor receptor 3 and the adapter protein SH2-B. A role in STAT5 activation. J Biol Chem277: 15962-15970

DOI

51
Kotani K, Wilden P, Pillay TS (1998) SH2-Balpha is an insulinreceptor adapter protein and substrate that interacts with the activation loop of the insulin-receptor kinase. Biochem J335(Pt 1): 103-109

52
Krebs DL, Uren RT, Metcalf D, Rakar S, Zhang JG, Starr R, De Souza DP, Hanzinikolas K, Eyles J, Connolly LM (2002) SOCS-6 binds to insulin receptor substrate 4, and mice lacking the SOCS-6 gene exhibit mild growth retardation. Mol Cell Biol22: 4567-4578

DOI

53
Kwon YK, Jang HJ, Kole S, He HJ, Bernier M (2003) Role of the pleckstrin homology domain of PLCgamma1 in its interaction with the insulin receptor. J Cell Biol163: 375-384

DOI

54
Lammers R, Bossenmaier B, Cool DE, Tonks NK, Schlessinger J, Fischer EH, Ullrich A (1993) Differential activities of protein tyrosine phosphatases in intact cells. J Biol Chem268: 22456-22462

55
Laurino JP, Colca JR, Pearson JD, DeWald DB, McDonald JM (1988) The in vitro phosphorylation of calmodulin by the insulin receptor tyrosine kinase. Arch Biochem Biophys265: 8-21

DOI

56
Lavan BE, Fantin VR, Chang ET, Lane WS, Keller SR, Lienhard GE (1997a) A novel 160-kDa phosphotyrosine protein in insulintreated embryonic kidney cells is a new member of the insulin receptor substrate family. J Biol Chem272: 21403-21407

DOI

57
Lavan BE, Lane WS, Lienhard GE (1997b) The 60-kDa phosphotyrosine protein in insulin-treated adipocytes is a new member of the insulin receptor substrate family. J Biol Chem272: 11439-11443

DOI

58
Le MN, Kohanski RA, Wang LH, Sadowski HB (2002) Dual mechanism of signal transducer and activator of transcription 5 activation by the insulin receptor. Mol Endocrinol16: 2764-2779

DOI

59
Lehr S, Kotzka J, Herkner A, Sikmann A, Meyer HE, Krone W, Muller-Wieland D (2000) Identification of major tyrosine phosphorylation sites in the human insulin receptor substrate Gab-1 by insulin receptor kinase in vitro. Biochemistry39: 10898-10907

DOI

60
Lemay S, Davidson D, Latour S, Veillette A (2000) Dok-3, a novel adapter molecule involved in the negative regulation of immunoreceptor signaling. Mol Cell Biol20: 2743-2754

DOI

61
Li Y, Soos TJ, Li X, Wu J, Degennaro M, Sun X, Littman DR, Birnbaum MJ, Polakiewicz RD (2004) Protein kinase C Theta inhibits insulin signaling by phosphorylating IRS1 at Ser(1101). J Biol Chem279: 45304-45307

DOI

62
Lin WH, Huang CJ, Liu MW, Chang HM, Chen YJ, Tai TY, Chuang LM (2001) Cloning, mapping, and characterization of the human sorbin and SH3 domain containing 1 (SORBS1) gene: a protein associated with c-Abl during insulin signaling in the hepatoma cell line Hep3B. Genomics74: 12-20

DOI

63
Liu F, Roth RA (1995) Grb-IR: a SH2-domain-containing protein that binds to the insulin receptor and inhibits its function. Proc Natl Acad Sci USA92: 10287-10291

DOI

64
Ma YM, Tao RY, Liu Q, Li J, Tian JY, Zhang XL, Xiao ZY, Ye F (2011) PTP1B inhibitor improves both insulin resistance and lipid abnormalities in vivo and in vitro. Mol Cell Biochem357: 65-72

DOI

65
Maddux BA, Goldfine ID (2000) Membrane glycoprotein PC-1 inhibition of insulin receptor function occurs via direct interaction with the receptor alpha-subunit. Diabetes49: 13-19

DOI

66
Masse K, Bhamra S, Allsop G, Dale N, Jones EA (2010) Ectophosphodiesterase/ nucleotide phosphohydrolase (Enpp) nucleotidases: cloning, conservation and developmental restriction. Int J Dev Biol54: 181-193

DOI

67
Mathews ST, Chellam N, Srinivas PR, Cintron VJ, Leon MA, Goustin AS, Grunberger G (2000) Alpha2-HSG, a specific inhibitor of insulin receptor autophosphorylation, interacts with the insulin receptor. Mol Cell Endocrinol164: 87-98

DOI

68
McAteer JB, Prudente S, Bacci S, Lyon HN, Hirschhorn JN, Trischitta V, Florez JC, Consortium E (2008) The ENPP1 K121Q polymorphism is associated with type 2 diabetes in European populations: evidence from an updated meta-analysis in 42, 042 subjects. Diabetes57: 1125-1130

DOI

69
Mitchell F (2012) Obesity: glypican-4: role in insulin signalling. Nat Rev Endocrinol8: 505

DOI

70
Moodie SA, Alleman-Sposeto J, Gustafson TA (1999) Identification of the APS protein as a novel insulin receptor substrate. J Biol Chem274: 11186-11193

DOI

71
Mooney RA, Senn J, Cameron S, Inamdar N, Boivin LM, Shang Y, Furlanetto RW (2001) Suppressors of cytokine signaling-1 and-6 associate with and inhibit the insulin receptor. A potential mechanism for cytokine-mediated insulin resistance. J Biol Chem276: 25889-25893

DOI

72
Moore AF, Jablonski KA, Mason CC, McAteer JB, Arakaki RF, Goldstein BJ, Kahn SE, Kitabchi AE, Hanson RL, Knowler WC (2009) The association of ENPP1 K121Q with diabetes incidence is abolished by lifestyle modification in the diabetes prevention program. J Clin Endocrinol Metab94: 449-455

DOI

73
Nouaille S, Blanquart C, Zilberfarb V, Boute N, Perdereau D, Roix J, Burnol AF, Issad T (2006) Interaction with Grb14 results in sitespecific regulation of tyrosine phosphorylation of the insulin receptor. EMBO Rep7: 512-518

74
O’Neill TJ, Zhu Y, Gustafson TA (1997) Interaction of MAD2 with the carboxyl terminus of the insulin receptor but not with the IGFIR. Evidence for release from the insulin receptor after activation. J Biol Chem272: 10035-10040

DOI

75
Patti ME, Sun XJ, Bruening JC, Araki E, Lipes MA, White MF, Kahn CR (1995) 4PS/insulin receptor substrate (IRS)-2 is the alternative substrate of the insulin receptor in IRS-1-deficient mice. J Biol Chem270: 24670-24673

DOI

76
Picardi PK, Calegari VC, Prada PO, Moraes JC, Araujo E, Marcondes MC, Ueno M, Carvalheira JB, Velloso LA, Saad MJ (2008) Reduction of hypothalamic protein tyrosine phosphatase improves insulin and leptin resistance in diet-induced obese rats. Endocrinology149: 3870-3880

DOI

77
Pillay TS, Sasaoka T, Olefsky JM (1995) Insulin stimulates the tyrosine dephosphorylation of pp125 focal adhesion kinase. J Biol Chem270: 991-994

DOI

78
Poy MN, Ruch RJ, Fernstrom MA, Okabayashi Y, Najjar SM (2002a) Shc and CEACAM1 interact to regulate the mitogenic action of insulin. J Biol Chem277: 1076-1084

DOI

79
Poy MN, Yang Y, Rezaei K, Fernstrom MA, Lee AD, Kido Y, Erickson SK, Najjar SM (2002b) CEACAM1 regulates insulin clearance in liver. Nat Genet30: 270-276

DOI

80
Rosenzweig T, Aga-Mizrachi S, Bak A, Sampson SR (2004) Src tyrosine kinase regulates insulin-induced activation of protein kinaseC (PKC) delta in skeletal muscle. Cell Signal16: 1299-1308

DOI

81
Rui L, Carter-Su C (1998) Platelet-derived growth factor (PDGF) stimulates the association of SH2-Bbeta with PDGF receptor and phosphorylation of SH2-Bbeta. J Biol Chem273: 21239-21245

DOI

82
Sacks DB, McDonald JM (1988) Insulin-stimulated phosphorylation of calmodulin by rat liver insulin receptor preparations. J Biol Chem263: 2377-2383

83
Sacks DB, McDonald JM (1989) Calmodulin as substrate for insulinreceptor kinase. Phosphorylation by receptors from rat skeletal muscle. Diabetes38: 84-90

DOI

84
Sacks DB, Fujita-Yamaguchi Y, Gale RD, McDonald JM (1989) Tyrosine-specific phosphorylation of calmodulin by the insulin receptor kinase purified from human placenta. Biochem J263: 803-812

85
Sacks DB, Davis HW, Crimmins DL, McDonald JM (1992) Insulinstimulated phosphorylation of calmodulin. Biochem J286(Pt 1): 211-216

86
Sacks DB, Mazus B, Joyal JL (1995) The activity of calmodulin is altered by phosphorylation: modulation of calmodulin function by the site of phosphate incorporation. Biochem J312(Pt 1): 197-204

87
Sadowski CL, Choi TS, Le M, Wheeler TT, Wang LH, Sadowski HB (2001) Insulin Induction of SOCS-2 and SOCS-3 mRNA expression in C2C12 Skeletal Muscle Cells Is Mediated by Stat5*. J Biol Chem276: 20703-20710

DOI

88
Salmeen A, Andersen JN, Myers MP, Tonks NK, Barford D (2000) Molecular basis for the dephosphorylation of the activation segment of the insulin receptor by protein tyrosine phosphatase 1B. Mol Cell6: 1401-1412

DOI

89
Samuel VT, Liu ZX, Wang A, Beddow SA, Geisler JG, Kahn M, Zhang XM, Monia BP, Bhanot S, Shulman GI (2007) Inhibition of protein kinase Cepsilon prevents hepatic insulin resistance in nonalcoholic fatty liver disease. J Clin Invest117: 739-745

DOI

90
Sanchez-Margalet V, Najib S (1999) p68 Sam is a substrate of the insulin receptor and associates with the SH2 domains of p85 PI3K. FEBS Lett455: 307-310

DOI

91
Sanchez-Margalet V, Najib S (2001) Sam68 is a docking protein linking GAP and PI3K in insulin receptor signaling. Mol Cell Endocrinol183: 113-121

DOI

92
Sanchez-Margalet V, Gonzalez-Yanes C, Najib S, Fernandez-Santos JM, Martin-Lacave I (2003) The expression of Sam68, a protein involved in insulin signal transduction, is enhanced by insulin stimulation. Cell Mol Life Sci60: 751-758

DOI

93
Sasaoka T, Kobayashi M (2000) The functional significance of Shc in insulin signaling as a substrate of the insulin receptor. Endocr J47: 373-381

DOI

94
Saville MK, Houslay MD (1994) Phosphorylation of calmodulin on Tyr99 selectively attenuates the action of calmodulin antagonists on type-I cyclic nucleotide phosphodiesterase activity. Biochem J299(Pt 3): 863-868

95
Sawka-Verhelle D, Filloux C, Tartare-Deckert S, Mothe I, Van Obberghen E (1997) Identification of Stat 5B as a substrate of the insulin receptor. Eur J Biochem250: 411-417

DOI

96
Sawka-Verhelle D, Tartare-Deckert S, Decaux JF, Girard J, Van Obberghen E (2000) Stat 5B, activated by insulin in a Jakindependent fashion, plays a role in glucokinase gene transcription. Endocrinology141: 1977-1988

DOI

97
Sciacchitano S, Taylor SI (1997) Cloning, tissue expression, and chromosomal localization of the mouse IRS-3 gene. Endocrinology138: 4931-4940

DOI

98
Seely BL, Staubs PA, Reichart DR, Berhanu P, Milarski KL, Saltiel AR, Kusari J, Olefsky JM (1996) Protein tyrosine phosphatase 1B interacts with the activated insulin receptor. Diabetes45: 1379-1385

DOI

99
Senn JJ, Klover PJ, Nowak IA, Zimmers TA, Koniaris LG, Furlanetto RW, Mooney RA (2003) Suppressor of cytokine signaling-3 (SOCS-3), a potential mediator of interleukin-6-dependent insulin resistance in hepatocytes. J Biol Chem278: 13740-13746

DOI

100
Shome K, Vasudevan C, Romero G (1997) ARFproteinsmediate insulindependent activation of phospholipase D. Curr Biol7: 387-396

DOI

101
Smith FM, Holt LJ, Garfield AS, Charalambous M, Koumanov F, Perry M, Bazzani R, Sheardown SA, Hegarty BD, Lyons RJ (2007) Mice with a disruption of the imprinted Grb10 gene exhibit altered body composition, glucose homeostasis, and insulin signaling during postnatal life. Mol Cell Biol27: 5871-5886

DOI

102
Srinivas PR, Wagner AS, Reddy LV, Deutsch DD, Leon MA, Goustin AS, Grunberger G (1993) Serum alpha 2-HS-glycoprotein is an inhibitor of the human insulin receptor at the tyrosine kinase level. Mol Endocrinol7: 1445-1455

DOI

103
Storz P, Doppler H, Pfizenmaier K, Muller G (1999) Insulin selectively activates STAT5b, but not STAT5a, via a JAK2-independent signalling pathway in Kym-1 rhabdomyosarcoma cells. FEBS Lett464: 159-163

DOI

104
Suchy D, Labuzek K, Machnik G, Kozlowski M, Okopien B (2013) SOCS and diabetes-ups and downs of a turbulent relationship. Cell Biochem Funct31: 181-195

DOI

105
Sun XJ, Crimmins DL, Myers MG Jr, Miralpeix M, White MF (1993) Pleiotropic insulin signals are engaged by multisite phosphorylation of IRS-1. Mol Cell Biol13: 7418-7428

106
Taniguchi CM, Emanuelli B, Kahn CR (2006) Critical nodes in signalling pathways: insights into insulin action. Nat Rev Mol Cell Biol7: 85-96

DOI

107
Tanti JF, Ceppo F, Jager J, Berthou F (2012) Implication of inflammatory signaling pathways in obesity-induced insulin resistance. Front Endocrinol ( Lausanne)3: 181

108
Tonks NK (2006) Protein tyrosine phosphatases: from genes, to function, to disease. Nat Rev Mol Cell Biol7: 833-846

DOI

109
Uchida T, Matozaki T, Noguchi T, Yamao T, Horita K, Suzuki T, Fujioka Y, Sakamoto C, Kasuga M (1994) Insulin stimulates the phosphorylation of Tyr538 and the catalytic activity of PTP1C, a protein tyrosine phosphatase with Src homology-2 domains. J Biol Chem269: 12220-12228

110
Ueki K, Kondo T, Kahn CR (2004) Suppressor of cytokine signaling 1 (SOCS-1) and SOCS-3 cause insulin resistance through inhibition of tyrosine phosphorylation of insulin receptor substrate proteins by discrete mechanisms. Mol Cell Biol24: 5434-5446

DOI

111
Ussar S, Bezy O, Bluher M, Kahn CR (2012) Glypican-4 enhances insulin signaling via interaction with the insulin receptor and serves as a novel adipokine. Diabetes61: 2289-2298

DOI

112
Van Horn DJ, Myers MG Jr, Backer JM (1994) Direct activation of the phosphatidylinositol 3’-kinase by the insulin receptor. J Biol Chem269: 29-32

113
Waltermann C, Klipp E (2011) Information theory based approaches to cellular signaling. Biochim Biophys Acta1810: 924-932

DOI

114
Wang J, Riedel H (1998) Insulin-like growth factor-I receptor and insulin receptor association with a Src homology-2 domaincontaining putative adapter. J Biol Chem273: 3136-3139

DOI

115
Wang LL, Richard S, Shaw AS (1995) P62 association with RNA is regulated by tyrosine phosphorylation. J Biol Chem270: 2010-2013

DOI

116
Wang X, Chen L, Maures TJ, Herrington J, Carter-Su C (2004) SH2- B is a positive regulator of nerve growth factor-mediated activation of the Akt/Forkhead pathway in PC12 cells. J Biol Chem279: 133-141

DOI

117
Wang L, Balas B, Christ-Roberts CY, Kim RY, Ramos FJ, Kikani CK, Li C, Deng C, Reyna S, Musi N (2007) Peripheral disruption of the Grb10 gene enhances insulin signaling and sensitivity in vivo. Mol Cell Biol27: 6497-6505

DOI

118
Waters SB, Pessin JE (1996) Insulin receptor substrate 1 and 2 (IRS1 and IRS2): what a tangled web we weave. Trends Cell Biol6: 1-4

DOI

119
White MF, Kahn CR (1994) The insulin signaling system. J Biol Chem269: 1-4

120
Wick MJ, Dong LQ, Hu D, Langlais P, Liu F (2001) Insulin receptormediated p62dok tyrosine phosphorylation at residues 362 and 398 plays distinct roles for binding GTPase-activating protein and Nck and is essential for inhibiting insulin-stimulated activation of Ras and Akt. J Biol Chem276: 42843-42850

DOI

121
Wick KR, Werner ED, Langlais P, Ramos FJ, Dong LQ, Shoelson SE, Liu F (2003) Grb10 inhibits insulin-stimulated insulin receptor substrate (IRS)-phosphatidylinositol 3-kinase/Akt signaling pathway by disrupting the association of IRS-1/IRS-2 with the insulin receptor. J Biol Chem278: 8460-8467

DOI

122
Williams JP, Jo H, Sacks DB, Crimmins DL, Thoma RS, Hunnicutt RE, Radding W, Sharma RK, McDonald JM (1994) Tyrosinephosphorylated calmodulin has reduced biological activity. Arch Biochem Biophys315: 119-126

DOI

123
Wong EC, Sacks DB, Laurino JP, McDonald JM (1988) Characteristics of calmodulin phosphorylation by the insulin receptor kinase. Endocrinology123: 1830-1836

DOI

124
Xu H, LeeK W, Goldfarb M (1998) Novel recognition motif on fibroblast growth factor receptor mediates direct association and activation of SNTadapter proteins. J Biol Chem273: 17987-17990

DOI

125
Yokouchi M, Suzuki R, Masuhara M, Komiya S, Inoue A, Yoshimura A (1997) Cloning and characterization of APS, an adaptor molecule containing PH and SH2 domains that is tyrosine phosphorylated upon B-cell receptor stimulation. Oncogene15: 7-15

DOI

126
Yu C, Chen Y, Cline GW, Zhang D, Zong H, Wang Y, Bergeron R, Kim JK, Cushman SW, Cooney GJ (2002) Mechanism by which fatty acids inhibit insulin activation of insulin receptor substrate-1 (IRS-1)-associated phosphatidylinositol 3-kinase activity in muscle. J Biol Chem277: 50230-50236

DOI

127
Zeng L, Sachdev P, Yan L, Chan JL, Trenkle T, McClelland M, Welsh J, Wang LH (2000) Vav3 mediates receptor protein tyrosine kinase signaling, regulates GTPase activity, modulates cell morphology, and induces cell transformation. Mol Cell Biol20: 9212-9224

DOI

128
Zhang W, Zong CS, Hermanto U, Lopez-Bergami P, Ronai Z, Wang LH (2006) RACK1 recruits STAT3 specifically to insulin and insulin-like growth factor 1 receptors for activation, which is important for regulating anchorage-independent growth. Mol Cell Biol26: 413-424

DOI

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