Encyclopedia
Phosphoinositides play a crucial role in regulating many cellular functions, such as actin dynamics, signaling, intracellular trafficking, membrane dynamics, and cell–matrix adhesion. Central to this process is phosphatidylinositol bisphosphate (PIP2). The levels of PIP2 in the membrane are rapidly altered by the activity of phosphoinositide-directed kinases and phosphatases, and it binds to dozens of different intracellular proteins. Despite the vast literature dedicated to understanding the regulation of PIP2 in cells over past 30 years, much remains to be learned about its cellular functions. In this review, we focus on past and recent exciting results on different molecular mechanisms that regulate cellular functions by binding of specific proteins to PIP2 or by stabilizing phosphoinositide pools in different cellular compartments. Moreover, this review summarizes recent findings that implicate dysregulation of PIP2 in many diseases.
- Phosphoinositides
- PIP2
- Cellular signaling pathways
- intracellular trafficking
- Cancer
- actin dynamics
- membrane dynamics
- Focal adhesion
- diseases
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1. Introduction
Phosphoinositides (PPIs), are inositol-containing glycerophospholipids bearing variable numbers of phosphate groups on their headgroups [1]. PPIs are multifaceted molecules that have recently become an interesting player in regulating cell function due to their involvement in cellular functions such as actin dynamics, membrane trafficking, regulation of transmembrane proteins and signal transduction [2,3,4,5,6,7,8]. Although the total amount of PPIs in eukaryotic cell membranes is low, they play critical roles in cellular dynamics by regulating multiprotein complexes [9,10]. The spatiotemporal regulation of PPI-mediated biological processes is achieved by interconversion (Figure 1) of the phosphorylation states of PPIs by specific kinases and phosphatases, followed by recruitment of PPI-specific effectors. Inter-conversion of the phosphate groups is spatially controlled by phosphoinositide-metabolizing kinases and phosphatases as required for cellular functions [11,12]. PPIs generate seven possible isoforms by phosphorylating the inositol ring at positions 3, 4, and 5. Three isoforms of PPIs with two phosphate groups connected to the inositol ring, phosphatidylinositol-(4,5)-bisphosphate (PI(4, 5)P2), phosphatidylinositol-(3,5)-bisphosphate (PI(3, 5)P2) and phosphatidylinositol-(3,4)-bisphosphate (PI(3, 4)P2) are the focus of this review. PI(3,4)P2 and PI(3,5)P2 are produced by the phosphorylation of PI3P, and PI(4,5)P2 is produced by the phosphorylation of PI4P or PI5P. The synthesis of PIP2 by phosphorylation of PI5P is regulated by PIP4K, which is one of the less studied pathways. In addition, PIP4K is able to phosphorylate PI3P, but only able to alter PI5P levels in vivo [13] (PI(4, 5)P2) can be further phosphorylated to (PI(3,4,5)P3) and (PI(3,4,5)P3) is converted to (PI(4,5)P2) by the enzyme phosphate and tensin homolog deleted from chromosome 10 (PTEN) [14]. PIP3 stimulates the activity of PDK1 and phosphorylates Akt [15,16]. This PIP3/Akt pathway is intensively studied and regulates many crucial processes in cells. PIP3 and PTEN have been the subjects of excellent recent reviews, and the focus here is on PIP2 [7].
Phosphoinositides control intracellular trafficking, membrane dynamics and cytoskeletal organization by interacting with many different proteins [17,18,19]. PIP2 regulates other membrane phospholipids and their signaling functions [7,17]. The major roles it plays in the cell membrane include cytoskeletal linkage, regulation of ion channels, and intracellular trafficking [20]. PI dynamics and mechanism are precisely controlled by kinase and phosphatase [21,22]. Recent studies showed the direct implication of these enzymes in diseases including liver cancer, glioblastoma or neurodegeneration [7,11,23]. Thus, many studies target phosphoinositide kinase inhibitors for pathological studies.
2. PIP2 in Actin Dynamics
Cytoskeletal dynamics play an important role in many cellular functions such as force generation, intracellular transport, or migration [24,25,26,27]. Actin forms the network inside the cell which is the most responsible for cellular architecture providing the cell a mechanical scaffold [24,27,28]. Accumulated evidence suggests that membrane PIP2 regulates the function of many acting binding proteins including formin, gelsolin, cofilin, profilin, filamin, WASP, ezrin, α- actinin, and others, which control the dynamical organization of the actin network [9,29,30,31,32,33]. PIP2 mostly inactivates actin binding proteins that inhibit actin polymerization and activates proteins which promote filamentous assembly [30,34]. Proteins bind to PIPs via numerus different structures, including the pleckstrin homology (PH) domain of phospholipase C-delta1, the Gag precursor protein Pr55 of HIV-1, phox homology (PX), C2, SH2, protein tyrosine binding, FYVE, PHD, GRAM, BAR, and espin N-terminal homology (ENTH)/ANTH domains, forming a large family of domains collectively [35,36].
Actin polymerization is regulated by a variety of actin binding proteins [28,37]. Actin dynamics depend upon the continuous attachment of G- actin at the barbed (+) end and dissociation at the pointed (−) end, and that defines the filament length [38]. Cofilin is an actin binding protein that binds to both F-actin and G-actin and is a severing protein responsible for actin depolymerization (Figure 2) [38,39,40]. ADF/ cofilin binds to PIP2 through a multivalent mechanism and the dissociation of ADF/cofilin to actin filament can accurately be regulated by changing PIP2 density at the cell membrane [41]. One study found that cofilin binds to PIP2 via a specific pocket which is pH dependent [42]. However, this result contrasts with recent finding showing that cofilin interaction with PIP2 is not pH dependent, but the interaction of profilin with membrane, actin and multiple PIP2 headgroup (clustering) is affected somewhat when pH is increased [41]. Cofilin’s activity depends on phosphorylation, which is regulated by Rho-GTPase and LIM kinase (LIMK) and by binding PPIs [43]. The rho-family small GTPases, Rho, Rac, and Cdc42, play a central role in regulating actin reorganization through their various downstream effectors [44]. LIMK1 and LIMK2 are activated by the GTPase-dependent protein kinases ROCK and PAK1 by phosphorylation of Thr508 and Thr-505, respectively, in the activation loop of the kinase domain [4,45]. LIMK1 and LIMK2 both regulate actin cytoskeletal reorganization by phosphorylating and inactivating cofilin/ADF [4,6]. Hence, cofilin is regulated by the signals from both the Rho and Rac pathways. Epidermal growth factor (EGF) induces sudden loss of PIP2 in membrane that activates local cofilin pool in membrane in carcinoma [46]. These altogether lead to a dramatic turnover of actin monomers (Figure 2).
Figure 2. Role of PIP2 in actin dynamics either by promoting polymerization or inhibiting severing. The figure summarizes gelsolin, profilin, cofilin, Arp2/3, and WASP dynamics in coordination with Rho- ROCK and Rac pathways.
3. PIP2 in Adhesion Dynamics
PIP2 binds to many focal adhesion proteins, such as vinculin, talin, and the focal adhesion kinase FAK. PIP2 serves as linkage to focal adhesion and actin binding proteins. There are actin binding proteins such as α-actinin, ezrin or filamin which also bind to focal adhesions. A synthetic peptide of α-actinin inhibits PLC-γ1 and PLC-δ1 activity and inhibition is induced by PIP2 competition [40]. PIP2 binding to α-actinin is inhibited by the treatment of cells with platelet derived growth factor, resulting in actin depolymerization. A recent study showed that the architecture of α-actinin-2 and 3 provides a suitable spatial orientation platform for PIP2 bonding by performing molecular dynamics (MD) simulations [65]. In smooth muscle in which α-actinin was discovered, PIP2 is found in large amounts which facilitates gelation of actin [66,67]. The length of smooth muscle depends upon the PIP2 synthesis, which regulates inositol phospholipid turnover [68]. Filamin A is another crosslinker protein which forms contacts between focal adhesions and F-actin. Filamin is associated to the cell membrane by β integrins. PIP2 bound to filamin A inhibits the gel formation of actin. Filamin has three isoforms called FLNa, FLNb, and FLNc. FLNa is recruited by CD28 followed by lipid raft accumulation at the immunological synapsis in T lymphocyte activation. PIP2 is essential for the clustering of lipid raft [69]. Ezrin is one of the ERM (ezrin, radixin, moesin) family proteins, which also forms linkages between the cellular membrane and cytoskeleton. Ezrin exists in both active and inactive states within cells. PIP2 activates Ezrin by binding with it and becomes available for phosphorylation by Rho-kinase and many PKC isoforms [70]. Neutron scattering experiment showed for the first-time, the conformational changes of ezrin when it simultaneously binds to PIP2 and F-actin [71].
Focal adhesion kinase (FAK) is a protein tyrosine kinase implicated in many signaling pathways to regulate cellular functions including migration. When a cell binds to the extracellular matrix (ECM), FAK is recruited to focal adhesion (FA) sites and undergoes conformational change, which is activated by phospholipids such as PIP2 by unblocking the FERM domain and kinase domain. Simulation results show that FAK transiently binds to PIP2 through electrostatic interactions [72]. Molecular dynamics simulation and fluorescence resonance energy transfer (FRET) experiments both showed that FAK binding to ATP decreases the FRET signal confirming that the PIP2 binding acts in the reverse direction [73,74]. Phosphatidylinositol 4-phosphate 5-kinase type Iγ (PIP5KIγ) is required for efficient FAK activation and generates PIP2 locally in FAs by PIP5KIγ. Thus, PIP2 is a strong mediator in integrin-FAK signaling pathways [73].
Talin plays a crucial role in activating integrins [75,76]. Within the cytosol talin is in an inactivated form, where its C-terminal rod domain binds to the N-terminal head domain. Many pathways lead to disruption of the interaction between talin’s C-terminal and N-terminal including binding with PIP5KIγ which generates PIP2 from PI4P [77]. Ye et al. delineate a detailed account of PIP2 in activating talin by using FRET. They showed interaction of talin with lipid bilayers is altered by PIP2 [78]. The FERM domain of talin-1 binds to the cytosolic domain of β3 -integrin weakly (Figure 3). However, the interaction affinity increases three-fold when it synergistically binds to acidic PIP2 [8,79,80]. Membrane bound talin recruits and activates vinculin. Vinculin localizes at the adhesion complex and interacts with PIP2 to associate with the membrane (Figure 3) [81]. Simulation data shows that PIP2 is not required for vinculin localization at FAs but is needed for the activation of FA turnover during mechanotransduction processes [81]. Other studies mentioned that PIP2 is required for FA formation and vinculin phosphorylation and trafficking [82].
Figure 3. Role of PIP2 in regulating focal adhesion assembly. Depiction of adhesion molecules talin, vinculin, ezrin, filamin and a-actinin. PIP2 synergistically binds to both talin and integrin and activates both of them. Talin binds directly to actin or activates vinculin and facilitates its binding to actin. PIP2 also binds to FERM domain of FAK and binds to vinculin via paxillin. PIP2 negatively regulates cross-linking activity of filamin and the actin bundle formation mediated by α-actinin.
4. Conclusions and outlook
Past evidence suggests that actin is connected to the membrane via actin binding proteins such as α-actinin or filamin which are regulated by phosphoinositides. These interactions also affect the binding of actin filaments with focal adhesion proteins such as paxillin, talin, FAK, or vinculin. The distribution of PIP2 in the membrane regulates cell signaling. PIP2 activity depends upon the concentration of cholesterol and divalent ions such as Ca2+, Mg2+, or Zn2+. In addition, PIP2 plays a crucial role in modulating many signaling pathways such as PIP3/Akt, mTORc1, or Rho dependent pathways that have implications in many diseases including cancer, neurodegenerative disease, or down syndrome.
Although PPIs are essential for many cellular functions, there are disparities in many processes which need further studies. PIP2 plays an important role in actin reorganization and filament dynamics. However, the role of PIP2 in any other cytoskeletal component has not yet been well studied. Among PIP2 binding actin proteins, LIMK1 and LIMK2 play an overlapping role in actin reorganization in the Rho-ROCK pathway. Further studies are required to differentiate the functional role of LIMK1 and LIMK2. Moreover, it is unclear if members of ROCK and PAK family proteins function as LIMK- activating kinases. Cortactin shows dependencies on PIP2 and Rac in dissociating from actin–myosin complex, although the direct implication of PIP2 in regulating cortactin still remains controversial [146], and other activators such as the endocytic protein Abp1p remain unclear. It has been shown that a synthetic peptide of α-actinin inhibits PLC-γ1 and PLC-δ1. It is ambiguous whether PIP2 bound to α-actinin is hydrolyzed by activated PLC-γ1 or not. The interaction of vinculin and membrane is based upon either full length or tail domain of vinculin in lipid bilayers or in cells. However, a specific lipid binding site has yet to be discovered.
This entry is adapted from the peer-reviewed paper 10.3390/ijms21218342
