A steady state analysis indicates that negative feedback regulation of PTP1B by Akt elicits bistability in insulin-stimulated GLUT4 translocation
© Giri et al; licensee BioMed Central Ltd. 2004
Received: 22 June 2004
Accepted: 03 August 2004
Published: 03 August 2004
The phenomenon of switch-like response to graded input signal is the theme involved in various signaling pathways in living systems. Positive feedback loops or double negative feedback loops embedded with nonlinearity exhibit these switch-like bistable responses. Such feedback regulations exist in insulin signaling pathway as well.
In the current manuscript, a steady state analysis of the metabolic insulin-signaling pathway is presented. The threshold concentration of insulin required for glucose transporter GLUT4 translocation was studied with variation in system parameters and component concentrations. The dose response curves of GLUT4 translocation at various concentration of insulin obtained by steady state analysis were quantified in-terms of half saturation constant.
We show that, insulin-stimulated GLUT4 translocation can operate as a bistable switch, which ensures that GLUT4 settles between two discrete, but mutually exclusive stable steady states. The threshold concentration of insulin required for GLUT4 translocation changes with variation in system parameters and component concentrations, thus providing insights into possible pathological conditions.
A steady state analysis indicates that negative feedback regulation of phosphatase PTP1B by Akt elicits bistability in insulin-stimulated GLUT4 translocation. The threshold concentration of insulin required for GLUT4 translocation and the corresponding bistable response at different system parameters and component concentrations was compared with reported experimental observations on specific defects in regulation of the system.
KeywordsInsulin signaling pathway GLUT4 Translocation Enzyme cascade Feedback loops Bistable switch
In living systems, extracellular information is processed through signal transduction machinery to appropriately regulate cellular function. This information processing machinery is made up of a complex web of enzyme cascades, allosteric interactions and feedback loops. Depending on their regulatory design these signaling networks elicit diverse responses, but display many common operating principles. A recurring theme in signaling systems is switch-like responses to graded or transient input signal. Various mechanisms are known to generate such all-or-none responses . Bistability is one such system level property, in which, the system switches between two discrete stable steady states without being able to rest in an intermediate state. Bistable systems exhibit hysteresis wherein, the value of input stimulus required for system transition from one state to another is quite different from the value required for reverse transition. Both computational and experimental analyses have shown that bistability plays a significant role in cellular differentiation and cell cycle progressions [2–5], production of biochemical memory , microbial metabolic systems , lateral signal propagation  and protein translocations . Existence of bistability in cellular regulation has been attributed to nonlinearity embedded in positive feedback loop or double negative feedback loop . Here, we present steady state simulation results of metabolic insulin signaling pathway comprising of positive feedback loops and show that this system can convert graded inputs into switch-like bistable output response.
Insulin is the most potent anabolic peptide hormone known that elicits myriad biological responses by specifically binding to insulin receptor and simultaneously stimulating multiple signaling pathways to regulate growth, differentiation and metabolism. Insulin maintains glucose homeostasis by stimulating the uptake, utilization and storage of glucose in muscle and adipose tissue, and inhibits hepatic glucose production . Defects in any of the pathway components lead to disturbance in growth, differentiation, and in the homeostasis of glucose and lipid levels. This leads to disease conditions such as type 2 diabetes, hypertension, obesity and a cluster of abnormalities characterized by insulin resistance or deficiency. In such a condition, normal circulating concentration of insulin is insufficient to elicit appropriate response [12, 13]. Studies over the last century have identified the major insulin signaling components involved in the regulation of glucose uptake into cells and its various defects in diseased states.
Although studies on various cell lines, transgenic and knock-out mice, have helped to uncover and characterize the different components involved in insulin signaling pathway, there are many voids in our understanding of the precise molecular mechanisms of signal transduction and cellular effects of insulin [16, 17]. The major hurdles are complexity of insulin signaling pathway and technical problems like experimental methodology employed for system level quantification. For example, depending upon different techniques employed, quantification of GLUT4 translocation in response to insulin binding yielded different results in the same cell type . Recent technical developments however have helped in studying the localization and translocation of signaling proteins and overall quantification of signaling processes in single cells has been possible . In such a scenario, it is pertinent to ask questions regarding the design principles involved in intracellular regulation. For example, what does a particular regulatory structure accomplish and how does it help in exhibiting different physiological responses. Based on available experimental data, computational and mathematical analysis can answer some of these questions and possibly propose new experiments and hypotheses. Earlier mathematical modeling studies of insulin signaling pathways have focused on subsystems of the pathway, like insulin receptor binding kinetics [20, 21], receptor recycling  and GLUT4 translocation [23–25]. Recently a comprehensive dynamic model of metabolic insulin signaling pathway was presented, which involved most of the known signaling components . Although the model correlated well with the published experiment data, authors did not discuss the system level regulatory design of insulin signaling system.
In the present work, we have developed a steady state model of insulin signaling to generate dose response curves for fractional translocation of GLUT4 to varying input insulin stimuli. One of the main objectives was to investigate the effect of inherent signaling structure made up of phosphorylation cycles, allosteric interactions and feedback loops on the system level response of insulin on GLUT4 translocation. Furthermore, we were interested in examining whether the regulatory design consisting of positive feedback loops in insulin signaling pathway exhibits bistable response. We solved the steady state equations for the entire metabolic insulin pathway including the positive feedback loops numerically, and found that GLUT4 gets translocated to the plasma membrane in an all-or-none manner in response to a varying concentration of input insulin stimuli. We show that GLUT4 translocation switches between the on-state and off-state and exhibits hysteresis in its response to increasing and decreasing input insulin concentration. This input-output relationship was then studied at various concentration of signaling components and system parameters in order to monitor the range over which this response persisted. We discuss these results by comparing with the known specific defects in regulation of the system (insulin dependent diseases) that lead to improper glucose uptake into the cell.
Insulin initiates its biological action by interacting with the insulin receptor, which belongs to a superfamily of tyrosine kinase receptors. On binding to the first insulin molecule, the receptor gets auto-phosphorylated and is dephosphorylated by phosphatase PTP1B . The phosphorylated insulin receptor can either bind with another insulin molecule or undergoes dissociation. Binding of the second insulin molecule does not affect the phosphorylation state of the receptor. Here we have assumed that the concentration of unbound phosphorylated receptor is negligible. Thus, phosphorylated receptors can exist as species bound to either singly or doubly bound molecules of insulin. Insulin bound phosphorylated receptor rapidly gets internalized into the endosomal apparatus of the cell before it gets dephosphorylated by PTP1B and incorporated into intracellular receptor pool . However recent studies indicate that, PTP1B might interact with insulin receptor directly and deactivate it without internalization . We have assumed that, the membrane bound phosphorylated insulin-receptor and its internalized form, both get dephosphorylated by PTP1B. The rate equation for intracellular receptor at steady state is represented as
where kp is rate constant and Kmr is Michaelis-Menten constant for dephosphorylation of internalized insulin receptors XIPi and XI2Pi. The term kd is first order degradation rate constant and ks is zero order synthesis rate constant of intracellular receptor Xi. The receptor exocytosis and endocytosis are assumed to be at quasi-equilibrium because of their faster time scales than the synthesis and degradation of receptors .
The phosphorylated active receptors further catalyze phosphorylation of several intracellular substrates including the IRS proteins, GAB-1, Shc and c-Cab1 . Among these, IRS-1 protein is known to participate in the regulation of GLUT4 translocation. In the present study we have assumed that, at steady state the twice-bound phosphorylated receptor catalyses the phosphorylation of IRS-1 protein while neglecting the activation of GAB-1, Shc, c-Cab1.
The phosphorylated active IRS-1 further binds and activates PI3 kinase and this association is assumed to occur with a stoichiometry of 1:1. Activated PI3 kinase further phosphorylates phosphatidylinositol-(4,5)-bisphosphate (PI-4,5-P2) to form phosphatidylinositol -3,4,5-triphosphate, (PIP3). The dephosphorylation of PIP3 to form PI-4,5-P2 is catalyzed by phosphatase PTEN, whereas, PIP3 is dephosphorylated to form PI-3,4-P2 by phosphatase SHIP2. Active PIP3 then is known to interact allosterically with phosphosinsositide-dependent kinase 1 (PDK1) and which in turn appears to phosphorylate kinase Akt (or protein kinase B) and protein kinase C-ζ (PKC-ζ) . However, as the interaction due to PDK1 is unclear, active PIP3 is assumed to play a role in phosphorylation of Akt and PKC-ζ. Since the parameters affecting the modification-demodification of Akt and PKC-ζ are considered to be similar, their modification is represented as a single enzyme cascade (Fig. 2).
The downstream elements of Akt and PKC-ζ, which effect GLUT4 translocation, are also unknown [11–13]. Therefore, we have assumed that phosphorylated Akt and PKC-ζ directly activate the GLUT4 translocation to the plasma membrane. In the basal state, GLUT4 slowly recycles between the plasma membrane and intracellular vesicular compartment. The phosphorylated Akt and PKC-ζ favor GLUT4 translocation (exocytosis) to the plasma membrane and thus increase glucose uptake as a response to insulin binding to the receptor . Here, total GLUT4 (Gt) is assumed to be sum of GLUT4 concentration in the cytosol (GC) and on the membrane (GM). The rate equation for GLUT4 species in cytoplasm at steady state is represented by,
where, k9 is the basal zero order synthesis rate of GLUT4, k10 is basal first order degradation rate, k11 is the insulin-activated GLUT4 exocytosis, k12 and k13 are basal first order rate of exocytosis and endocytosis, respectively. As assumed by Sedaghat, et al. , the basal equilibrium distribution of cell surface GLUT4 and GLUT4 in the intracellular pool are taken as 4% and 96%.
The insulin signaling pathway has been shown to consist of multiple feedback loops . Active Akt is known to phosphorylate and thereby negatively regulate the upstream phosphatase PTP1B. This phosphorylation impairs the ability of PTP1B to dephosphorylate insulin receptor and IRS-1 by 25% . This represents overall positive feedback loop as Akt inhibits signal attenuation enzyme PTP1B. The resulting circuit also represents a double negative feedback loop, in which phosphorylated protein negatively regulate the phosphatase that dephosphorylates it. To incorporate these feedback loops we assumed that active Akt affects the total active PTP1B enzyme and thus inhibits the dephosphorylation of the receptor and IRS-1. The feedback effect of Akt on PTP1B was incorporated by following relationship
where, [PTP]max is maximum PTP1B concentration, PTPt is the total active PTP1B concentration after incorporating the effects of feedback, AktP represents the phosphorylated Akt concentration influencing the PTPase activity, and kf represents the half saturation constant quantifying feedback. The value of kf was estimated based on the assumption that 25% of PTP1B is inactivated by total AktP . Thus, kf is appropriately calculated so that the first term [kf /[kf + AktP]] is equal to 0.75. In absence of feedback effects, PTPt equals PTPmax.
The set of equations given in 'appendix' and in 'methods' section were solved numerically using fsolve program of Matlab (The MathWorks Inc. USA). The accuracy of the simulation was verified by numerically checking the mass balance of all species. The steady state modeling of entire insulin signaling was evaluated including the feedback loops and estimating the fractions of GLUT4 translocated to the plasma membrane for a particular concentration of insulin. Thus, the overall action of insulin on GLUT4 translocation is quantified as,
where, f is fractional GLUT4 on plasma membrane, GM is GLUT4 concentration on plasma membrane and Gt is total GLUT4 concentration with respect to whole cell volume.
Bistability in GLUT4 translocation to plasma membrane
The observed hysteresis is characteristic of a bistable response obtained due to negative feedback regulation of upstream signal attenuation enzyme PTP1B by downstream kinase Akt. Experimental data available in the literature indicates a subsensitive response of insulin, requiring ~130 fold change in insulin concentration for the maximal GLUT4 translocation to plasma membrane . Our results show an ultrasensitive response in insulin-stimulated GLUT4 translocation due to bistability (~4-fold change in insulin concentration); however, the half saturation values match with that of experimental data. The response was ultrasensitive (Hill coefficient ~3.1) and not bistable in absence of feedback loops (curve a, Fig 3A).
Effect of system component concentration on GLUT4 translocation
To examine the influence of pathological conditions arising due to variations in protein expression levels on final output response of insulin, we varied the concentration of individual signaling components IRS-1, PI3K, lipids, PKC-ζ, Akt and phosphatases, PTP1B, PTEN and SHIP2 over a wide range. For each case, the dose response curve of fractional GLUT4 on the plasma membrane at various insulin concentrations was obtained and the response was quantified in-terms of half saturation constant. To illustrate this, we consider a case of increase in PTP1B concentration. Fig. 3B shows the dose response curves for insulin stimulated GLUT4 translocation at plasma membrane at two different concentrations of PTP1B. At high PTP1B concentration, the bistable dose response curve becomes monostable (but, still ultrasensitive) and shifts to the right. This indicates a nullifying effect of negative feedback regulation on PTP1B by Akt and higher requirement of insulin for maximal translocation of GLUT4. Thus, in Fig 3B curve 'a' and curve 'b' can be characterized by two and one half saturation values respectively.
To study the effect of signal attenuation enzymes such as phosphatases on the output response, the concentrations of PTP1B, PTEN and SHIP2 were altered over a wide range, keeping other parameters constant. Fig. 4C and 4D show the influence of variation in concentrations of PTP1B and PTEN on half saturation constant of insulin. Increase in PTP1B and PTEN concentration results in a drastic increase in the threshold concentration of insulin required to switch-on or switch-off GLUT4 translocation. This illustrates that more insulin than physiological concentration is required at higher phosphatase (PTP1B or PTEN) concentrations to translocate GLUT4 from cytoplasm to plasma membrane. For example, around 16-fold change in the insulin concentration is observed for a 1.5-fold increase in PTP1B concentration from 0.039 nM to 0.06 nM. The system looses bistability beyond a narrow range of PTP1B concentration between 0.02 nM to 0.05 nM. Thus, the response of GLUT4 translocation to insulin is particularly sensitive to PTP1B concentration.
Influence of feedback on GLUT4 translocation
The steady state analysis of metabolic insulin-signaling pathway demonstrated signal amplification as signal propagates down the cascades. The amount of insulin required for 50% activation of insulin receptor, IRS-1, PIP3, Akt, PKC-ζ and GLUT4 was estimated to decrease in presence or absence of feedback loops (results not shown).
Effect of system parameter values on GLUT4 translocation
In this work we have demonstrated that, the dose response curves of fractional GLUT4 concentration on plasma membrane at various concentration of insulin exhibit hysteresis-a property of bistable systems. The analysis of bistable response in presence of feedback loops was done at varying concentration of signaling components and system parameters in physiological range. The overall response of insulin demonstrated signal amplification as the signal propagates down the cascade, thus requiring less insulin for GLUT4 translocation. The insulin sensitivity increased by increasing the concentration of proteins that amplify the insulin action and decreasing the concentration of proteins that attenuate insulin-signaling pathway. This indicates that the bistability and the half saturation constant are dependent on the component concentrations and system parameters.
It is known that defects in insulin signaling pathway leads to pathological conditions like diabetes, wherein normal or elevated levels of insulin produces impaired biological response. This characteristic decrease or increase in insulin sensitivity is mainly attributed to post-receptor defects including mutational changes in protein expression levels or other parameters like dissociation constants and Michaelis-Menten constants [13, 33]. Numerous experimental studies like targeted deletions/mutations of signaling components have yielded insights about the disease states. In the present work, to study the influence of pathological conditions on final output response of insulin, the concentration of individual signaling components was varied over a wide range, by keeping other parameters constant. The predicted results are consistent with various reported experimental observations and thus validate our steady state model. (i) Decreased concentration of phosphorylated insulin receptor and IRS-1 are observed in muscle from morbidly obese subjects  and those with diabetes . This decreased phosphorylation can be either due to decrease in protein concentration itself or impaired phosphorylation event. (ii) Increase in the level and activity of several tyrosine phosphatases (PTP1B) was found to be associated with insulin resistance and reduced insulin sensitivity [12, 13, 33, 36]. (iii) Overexpression of PI3K and its downstream targets Akt and PKC in cell culture models increased GLUT4 translocation . (iv) Decrease in the association of PI3K with phosphorylated IRS-1 and subsequent activation appears to be a characteristic abnormality in type 2 diabetes and obesity [13, 33–35]. (v) Single gene knockout experiments have shown that, mice with PTP1B knockout , mice with SHIP2 knockout  and targeted deletion of PTEN in murine lever , all results in hypersensitivity towards insulin. In the present work, though we have not done in-silico perturbation analysis by deleting a particular protein, we have changed the concentration of specific protein over wide range to bring about the similar effect of deficiency. Thus, our simulation results show that the insulin sensitivity dramatically increased when we decreased the concentration of phosphatases like PTP1B, PTEN and SHIP2.
Increase in the concentration of Akt, makes the signal amplification increased along with slight increase in the degree of bistability. This effect is brought about by the enhanced nonlinearity in the feedback loop due to zero order ultrasensitivity  imposed by increasing the concentration of Akt or percentage feedback. At high Akt concentration (or when overexpressed), the system can respond in constitutively active mode or might also function as a memory module. That is, once insulin switches on the system, the high Akt concentration or percentage feedback by itself can keep the switch on even after insulin is removed. This may be the reason for the experimental observation of insulin independent GLUT4 translocation to plasma membrane when Akt is overexpressed [12, 40]. This insulin independent translocation of GLUT4 is thought to be due to activation of PI3K independent pathway or by amplification of residual signal. Our analysis indicates that the inherent feedback structure present in the insulin-signaling pathway by itself can induce this phenomenon.
Does GLUT4 translocation show a bistable response to insulin in-vivo?
Bistability has been shown to be the outcome of regulatory structure with feedback loops and non-linearity in the system . The non-linearity in the system is brought about by an ultrasensitive response typically obtained through enzyme cascades. Such ultrasensitive responses exhibit steep dose response curves with Hill coefficient greater than one . The cascade systems use energy for their operation and are optimally operated under zero order sensitivity (i.e., cascades operating under saturating interconvertable enzymes) requiring minimum energy [42, 43]. Presence of feedback loops may further optimize the requirement of energy. Enzyme cascades and multiple positive feedback loops are observed in insulin-signaling pathway. Experimental results have shown that the dose response curve of insulin-stimulated glucose uptake is subsensitive with a Hill coefficient of about 0.8 [calculated from ref. ]. Thus the question arises as to what may be the significance of the cascade signaling system with positive feedback loops in insulin signaling pathway. The reason for this discrepancy may be because, the experimental data represents a profile of glucose uptake in ensemble of cells , and furthermore, glucose uptake may not be proportional to the amount of GLUT4 on cell surface .
Recently, bistability has been experimentally demonstrated in many cellular regulation systems . Experiments on cellular differentiation and cell-cycle progression have shown that, to demonstrate bistability it is essential to measure the amount of input required to switch-on the system from a low activity state to a high activity state, and amount of input required to hold-on the system in high activity state [3–5]. Reynolds et al. , have shown experimentally that, the reaction network of PTPase inhibition by activated epidermal growth factor receptor (EGFR, a receptor tyrosine kinase, RTK) through reactive oxygen species, can generate highly amplified and switch like bistable response to a threshold concentration of ligand stimulus. In this system, PTPase is a negative regulator of active RTK and thus, PTPase inhibition by reactive oxygen species serves as a positive feedback loop.
Our simulation results indicate that similar bistable response can be obtained in insulin-stimulated GLUT4 translocation because of the positive feedback loops (inhibitory action of Akt on PTP1B). Though experimental verification of this property is awaited, there are indications that insulin signaling pathway possesses many requisite components to exhibit bistable response. The simulation results presented here showed that, the ultrasensitivity in absence of feedback effects and the regulatory structure of feedback loops are main reasons for a bistable response. Other than the positive feedback loops considered in the present work, Insulin signaling system is also known to contain many feedback loops which have not been entirely characterized . One possible reason for having so many interlocking positive feedback and negative feedback loops may be to cause oscillations in GLUT4 translocation or to make the bistability of GLUT4 translocation – more robust.
Recently, it has been shown that insulin stimulation in a variety of cell types elicit a rapid production of hydrogen peroxide and which reversibly inhibit PTP1B enhancing propagation of the early insulin signal . This regulatory mechanism was also found to be essential for PI3K mediated Akt activation, GLUT4 translocation to plasma membrane and insulin-stimulated glucose uptake . However, unlike EGFR system  existence of bistable behavior is yet to be shown in insulin signaling system. In insulin signaling pathway other than GLUT4, proteins like Akt and PKC get translocated to plasma membrane and such inter-compartmental translocations can also exhibit switch like bistable response .
It is becoming clear that quantification studies have to be performed in single cell rather than cell populations . This is true especially while addressing the system level questions like ultrasensitivity, bistability and oscillations [4–7, 46]. Recently, this was also found to be of immense value in case of insulin signaling pathway to uncover the PIP3 activation mode . Simultaneous measurement of PIP3 production and GLUT4 insertion in individual 3T3L1 adipocytes suggested that a threshold for PIP3 signals exists. Below this threshold, GLUT4 transporters are minimally inserted into the plasma membrane and their insertion increases once this threshold is overcome. In summary, it is essential to show through experiments that, the stimulus-response curve for insulin-stimulated GLUT4 translocation exhibits hysteresis, – a distinctive splitting in stimulus response curve. There should be a particular concentration of insulin, which is not sufficient to translocate GLUT4 to plasma membrane, but is sufficient to maintain GLUT4 on plasma membrane.
What may be the significance of such a bistable behavior in GLUT4 translocation? Though there is no obvious answer to this question yet, it is known that, bistability can maintain a biological response even when the input stimulus is brief and the high activity level is maintained only as long as the system requires. Insulin binding to its cell surface receptor is rapidly followed by internalization of insulin-receptor complex. This internalization of receptor has been implicated in receptor down regulation, attenuation of insulin sensitivity and insulin clearance from the circulation [12, 13]. Thus a brief input stimulation should be sufficient to balance the translocation of GLUT4 to plasma membrane and its reversal depending on glucose concentration. Additionally, due to small absolute stimulus concentrations, the probability of noise occurrence is high. A bistable response having distinct threshold concentration to switch-on and switch-off offers advantage in handling noise.
In cellular regulation, different structural motifs such as enzyme cascades, feedforward control and multiple feedback loops yield complex regulatory networks. These are shown to be responsible for exhibiting system level properties including bistability and robustness [10, 48, 49]. Other than multiple feedback loops, structural regulatory motifs like multisite covalent modification cycles have been shown to induce bistability . The interconnections between these regulatory motifs at the system level may elicit a multistable response to particular stimuli, which have to be theoretically uncovered and demonstrated through experiments.
Equilibrium relationships, rate equations, mass balance equations and model parameters used for simulation of metabolic insulin signaling system at steady state (refer Fig. 2 for nomenclature and interaction details). Equations were solved simultaneously, for evaluating fractional GLUT4 translocation at a particular insulin concentration, using fsolve function of Matlab (The MathWorks Inc. USA). Most of the values of model parameters for steady state analysis are taken from Sedaghat et al. . Nomenclature, parameter values are:
It, total insulin concentration varied over a wide range; Xt, total receptor = 0.003 nM; At, total IRS-1= 0.01 nM, Bt, total PI3-Kinase = 0.5 nM, PTENt, total PTEN= 0.007 nM; CP2t, total lipid = 0.01 nM; SHIP2t, total SHIP2 = 0.001 nM; Ft, total Akt+PKC-ξ = 0.02 nM, PTPmax, total PTP1B= 0.039 nM; Gt, total GLUT4 = 9 nM; E6t, total E6 = 0.001 nM; E8t, total E8 = 0.001 nM;
k0 = 2500 min-1; k = 0.2 min-1; k1= 4.16 min-1; k2 = 1.4 min-1; k3 = 50 min-1 (assumed); k4 = 42.1 min-1; k5 = 2.8 min-1; k6 = 3 min-1; k7 = 20 min-1 (assumed); k8 = 6.9 min-1; k9 = 0.11 min-1; k10 = 0.0012 min-1; k11 = 3.47 min-1 (assumed); k12 = 6.96*10-3 min-1; k13 = 0.17 min-1; kp = 0.461 min-1 ; kd = 1.67 × 10-18 min-1 ; ks = 1.67*10-25 nM min -1;
Kd1= 3.33 nM; Kd2 = 333.3 nM; Kd3 = 0.014 nM;
Kd4 = 9 nM; Kd5 = 0.1 nM;
Kmr, Km1 to Km8 = 10-4 nM
The total molar balances for different species are given below.
Rate expression with pseudo-steady state representation of complexes for modification-demodification cycles
Receptor autophosphorylation and dephosphorylation cycle
Glucose-transporter isoform 4
Phosphatidylinositol (PI)-3,4,5-tiphosphate (PI-3,4,5-P3)
Protein kinase Akt or protein kinase B (PKB)
Protein kinase C
Protein tyrosine phosphatase 1B
3' lipid phosphatase
5' lipid phosphatase
- Ferrell JE: Tripping the switch fantastic: how a protein kinase cascade can convert graded inputs into switch-like outputs. Trends Biochem Sci. 1996, 21: 460-466. 10.1016/S0968-0004(96)20026-X.View ArticlePubMedGoogle Scholar
- Bagowski CP, Ferrell JE: Bistability in the JNK cascade. Curr Biol. 2001, 11: 1176-1182. 10.1016/S0960-9822(01)00330-X.View ArticlePubMedGoogle Scholar
- Becskei A, Seraphin B, Serrano L: Positive feedback in eukaryotic gene networks: cell differentiation by graded to binary response conversion. EMBO J. 2001, 20: 2528-2535. 10.1093/emboj/20.10.2528.PubMed CentralView ArticlePubMedGoogle Scholar
- Pomerening JR, Sontag ED, Ferrell JE: Building a cell cycle oscillator: hysteresis and bistability in the activation of Cdc2. Nat Cell Biol. 2003, 5: 346-351. 10.1038/ncb954.View ArticlePubMedGoogle Scholar
- Sha W, Moore J, Chen K, Lassaletta AD, Yi CS, Tyson JJ, Sible JC: Hysteresis drives cell-cycle transitions in Xenopus laevis egg extracts. Proc Natl Acad Sci USA. 2003, 100: 975-980. 10.1073/pnas.0235349100.PubMed CentralView ArticlePubMedGoogle Scholar
- Xiong W, Ferrell JE: A positive-feedback-based bistable memory module that governs a cell fate decision. Nature. 2003, 426: 460-465. 10.1038/nature02089.View ArticlePubMedGoogle Scholar
- Ozbudak EM, Thattai M, Lim HN, Shraiman BI, Oudenaarden AV: Multistability in the lactose utilization network of Escherichia coli. Nature. 2004, 427: 737-740. 10.1038/nature02298.View ArticlePubMedGoogle Scholar
- Reynolds AR, Tischer C, Verveer PJ, Rocks O, Bastiens PIH: EGFR activation coupled to inhibition of tyrosine phosphatases causes lateral signal propagation. Nature Cell Biol. 2003, 5: 447-453. 10.1038/ncb981.View ArticlePubMedGoogle Scholar
- Teruel MN, Meyer T: Parallel signal-cell monitoring of receptor-triggered membrane translocation of a calcium-sensing protein module. Science. 2002, 295: 1910-1912. 10.1126/science.1065028.View ArticlePubMedGoogle Scholar
- Ferrell Jr: Self-perpetuating states in signal transduction: positive feedback, double-negative feedback and bistability. Curr Opin Chem Biol. 2002, 14: 140-148. 10.1016/S0955-0674(02)00314-9.View ArticleGoogle Scholar
- Saltiel AR, Kahn CR: Insulin signaling and the regulation of glucose and lipid metabolism. Nature. 2001, 414: 799-806. 10.1038/414799a.View ArticlePubMedGoogle Scholar
- Nystrom FH, Quon MJ: Insulin signalling: Metabolic pathways and mechanisms for specificity. Cell Signal. 1999, 11: 563-574. 10.1016/S0898-6568(99)00025-X.View ArticlePubMedGoogle Scholar
- Shepherd PR, Kahn BB: Glucose transporters and insulin action: implication for insulin resistance and diabetes mellitus. N Engl J Med. 1999, 341: 248-257. 10.1056/NEJM199907223410406.View ArticlePubMedGoogle Scholar
- Bryant NJ, Govers R, James DE: Regulated transport of the glucose transporter GLUT4. Nat Rev Mol Cell Biol. 2002, 3: 267-277. 10.1038/nrm782.View ArticlePubMedGoogle Scholar
- Johnston AM, Pirola L, Obberghen EV: Molecular mechanisms of insulin receptor substrate protein-mediated modulation of insulin signaling. FEBS Lett. 2003, 546: 32-36. 10.1016/S0014-5793(03)00438-1.View ArticlePubMedGoogle Scholar
- Saltiel AR, Pessin JE: Insulin signaling pathways in time and space. Trends Cell Biol. 2002, 12: 65-71. 10.1016/S0962-8924(01)02207-3.View ArticlePubMedGoogle Scholar
- Watson RT, Kanzaki M, Pessin JE: Regulated membrane trafficking of the insulin-responsive glucose transporter 4 in adipocytes. Endocrine Rev. 2004, 25: 177-204. 10.1210/er.2003-0011.View ArticleGoogle Scholar
- Kandror KV: A long search for GLUT4 activation. Sci STKE. 2003, PE5-169
- Meyer T, Teruel MN: Fluorescence imaging of signaling networks. Trends Cell Biol. 2003, 13: 101-106. 10.1016/S0962-8924(02)00040-5.View ArticlePubMedGoogle Scholar
- Shymko RM, Dumont E, De Meyts P, Dumont JE: Timing-dependence of insulin-receptor mitogenic versus metabolic signalling: a plausible model based on coincidence of hormone and effector binding. Biochem J. 1999, 339: 675-683. 10.1042/0264-6021:3390675.PubMed CentralView ArticlePubMedGoogle Scholar
- Wanant S, Quon MJ: Insulin receptor binding kinetics: modeling and simulation studies. J Theor Biol. 2000, 205: 355-364. 10.1006/jtbi.2000.2069.View ArticlePubMedGoogle Scholar
- Quon MJ, Campfield LA: A mathematical model and computer simulation study of insulin receptor regulation. J Theor Biol. 1991, 150: 59-72.View ArticlePubMedGoogle Scholar
- Quon MJ: Advances in kinetic analysis of insulin-stimulated GLUT-4 translocation in adipose cells. Am J Physiol. 1994, 266: E144-E150.PubMedGoogle Scholar
- Holman GD, Lo Leggio L, Cushman SW: Insulin-stimulated GLUT4 glucose transporter recycling. A problem in membrane protein subcellular trafficking through multiple pools. J Biol Chem. 1994, 269: 17516-17524.PubMedGoogle Scholar
- Quon MJ, Campfield LA: A mathematical model and computer simulation study of insulin-sensitive glucose transporter regulation. J Theor Biol. 1991, 150: 93-107.View ArticlePubMedGoogle Scholar
- Sedaghat AR, Sherman A, Quon MJ: A mathematical model of metabolic insulin signaling pathways. Am J Physiol Endocrinol Metab. 2002, 283: E1084-E1101.View ArticlePubMedGoogle Scholar
- Elmendorf JS: Signals that regulate GLUT4 translocation. J Membr Biol. 2002, 190: 167-174. 10.1007/s00232-002-1035-3.View ArticlePubMedGoogle Scholar
- Goldbeter A, Koshland DE: An amplified sensitivity arising from covalent modification in biological systems. Proc Natl Acad Sci USA. 1981, 78: 6840-6844.PubMed CentralView ArticlePubMedGoogle Scholar
- Di Guglielmo GM, Drake PG, Baass PC, Authier F, Posner BI, Bergeron JJM: Insulin receptor internalization and signaling. Mol Cell Biochem. 1998, 182: 59-63. 10.1023/A:1006883311233.View ArticlePubMedGoogle Scholar
- Shi K, Egawa K, Maegawa H, Nakamura T, Ugi S, Nishio Y, Kashiwagi A: Protein-Tyrosine Phosphatase 1B Associates with Insulin Receptor and Negatively Regulates Insulin Signaling without Receptor Internalization. J Biochem. 2004, 136: 89-96. 10.1093/jb/mvh094.View ArticlePubMedGoogle Scholar
- Ravichandran LV, Chen H, Li Y, Quon MJ: Phosphorylation of PTP1B at Ser (50) by Akt impairs its ability to dephosphorylate the insulin receptor. Mol Endocrinol. 2001, 15: 1768-1780. 10.1210/me.15.10.1768.View ArticlePubMedGoogle Scholar
- Stagsted J, Hansen T, Roth RA, Goldstein A, Olsson L: Correlation between insulin receptor occupancy and tyrosine kinase activity at low insulin concentrations and effect of major histocompatibility complex class I-derived peptide. J Pharmacol Exp Ther. 1993, 267: 997-1001.PubMedGoogle Scholar
- Pessin JE, Saltiel AR: Signaling pathways in insulin action: molecular targets of insulin resistance. J Clin Invest. 2000, 106: 165-169.PubMed CentralView ArticlePubMedGoogle Scholar
- Goodyear LJ, Giorgino F, Sherman LA, Carey J, Smith RJ, Dohm GL: Insulin receptor phosphorylation, insulin receptor substrate-1 phosphorylation, and phosphatidylinositol 3-kinase activity are decreased in intact skeletal muscle strips from obese subjects. J Clin Invest. 1995, 95: 2195-2204.PubMed CentralView ArticlePubMedGoogle Scholar
- Bjornholm M, Kawano Y, Lehtihet M, Zierath JR: Insulin receptor substrate-1 phosphorylation and phosphatidylinositol 3-kinase activity in skeletal muscle from NIDDM subjects after in vivo insulin stimulation. Diabetes. 1997, 46: 524-527.View ArticlePubMedGoogle Scholar
- Ahmad F, Azevedo JL, Cortright R, Dohm GL, Goldstein BJ: Alterations in skeletal muscle protein-tyrosine phosphatase activity and expression in insulin-resistant human obesity and diabetes. J Clin Invest. 1997, 100: 449-458.PubMed CentralView ArticlePubMedGoogle Scholar
- Elchebly M, Payette P, Michaliszyn E, Cromlish W, Collins S, Loy AL, Normandin D, Cheng A, Himms-Hagen J, Chan CC, Ramachandran C, Gresser MJ, Tremblay ML, Kennedy BP: Increased insulin sensitivity and obesity resistance in mice lacking the protein tyrosine phosphatase-1B gene. Science. 1999, 283: 1544-1548. 10.1126/science.283.5407.1544.View ArticlePubMedGoogle Scholar
- Clément S, Krause U, Desmedt F, Tanti JF, Behrends J, Pesesse X, Sasaki T, Penninger J, Doherty M, Malaisse W, Dumont JE, Le Marchand-Brustel Y, Erneux C, Hue L, Schurmans S: The lipid phosphatase SHIP2 controls insulin sensitivity. Nature. 2001, 409: 92-7. 10.1038/35051094.View ArticlePubMedGoogle Scholar
- Stiles B, Wang Y, Stahl A, Bassilian A, Lee WP, Kim YJ, Sherwin R, Devaskar S, Lesche R, Magnuson MA, Wu H: Liver-specific deletion of negative regulator PTEN results in fatty liver and insulin hypersensitivity. Proc Natl Acad Sci USA. 2004, 101: 2082-2087. 10.1073/pnas.0308617100.PubMed CentralView ArticlePubMedGoogle Scholar
- Cong LN, Chen H, Li Y, Zhou L, McGibbon MA, Taylor SI, Quon MJ: Physiological role of Akt in insulin-stimulated translocation of GLUT4 in transfected rat adipose cells. Mol Endocrinol. 1997, 11: 1881-1890. 10.1210/me.11.13.1881.View ArticlePubMedGoogle Scholar
- Angeli D, Ferrell JE, Sontag ED: Detection of multistability, bifurcations, and hysteresis in a large class of biological positive-feedback systems. Proc Natl Acad Sci USA. 2004, 101: 1822-1827. 10.1073/pnas.0308265100.PubMed CentralView ArticlePubMedGoogle Scholar
- Shacter E, Chock PB, Stadtman ER: Energy consumption in a cyclic phosphorylation/dephosphorylation cascade. J Biol Chem. 1984, 259: 12260-12264.PubMedGoogle Scholar
- Goldbeter A, Koshland DE: Energy expenditure in the control of biochemical systems by covalent modification. J Biol Chem. 1987, 262: 4460-4471.PubMedGoogle Scholar
- Mahadev K, Zilbering A, Zhu L, Goldstein BJ: Insulin-stimulated hydrogen peroxide reversibly inhibits protein tyrosine phosphatase 1B in-vivo and enhances the early insulin action cascade. J Biol Chem. 2001, 276: 21938-21942. 10.1074/jbc.C100109200.View ArticlePubMedGoogle Scholar
- Mahadev K, Wu X, Zilbering A, Zhu L, Todd J, Lawrence R, Goldstein BJ: Hydrogen peroxide generated during cellular insulin stimulation is integral to activation of the distal insulin signaling cascade in 3T3-L1 adipocytes. J Biol Chem. 2001, 276: 48662-48669. 10.1074/jbc.M105061200.View ArticlePubMedGoogle Scholar
- Ferrell JE, Machleder EM: The biochemical basis of an all-or-none cell fate switch in Xenopus oocytes. Science. 1998, 280: 895-898. 10.1126/science.280.5365.895.View ArticlePubMedGoogle Scholar
- Tengholm A, Meyer T: A PI3-kinase code for insulin-triggered insertion of glucose transporters into the plasma membrane. Curr Biol. 2002, 12: 1871-1876. 10.1016/S0960-9822(02)01223-X.View ArticlePubMedGoogle Scholar
- Bhalla US, Ram PT, Iyengar R: MAP kinase phosphatase as a locus of flexibility in a mitogen-activated protein kinase signaling network. Science. 2002, 297: 1018-1023. 10.1126/science.1068873.View ArticlePubMedGoogle Scholar
- Venkatesh KV, Bhartiya S, Ruhela A: Multiple feedback loops are key to dynamic performance of tryptophan regulation in Escherichia coli. FEBS Lett. 2004, 563: 234-240. 10.1016/S0014-5793(04)00310-2.View ArticlePubMedGoogle Scholar
- Markevich NI, Hoek JB, Kholodenko BN: Signaling switches and bistability arising from multisite phosphorylation in protein kinase cascades. J Cell Biol. 2004, 164: 353-359. 10.1083/jcb.200308060.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.