Analysis of Phosphatidylinositol 3,4,5-Trisphosphates of PTEN Expression on Mammalian Cells
Analysis of Phosphatidylinositol 3,4,5-Trisphosphates of PTEN Expression on Mammalian Cells
Mass Spectrometry Letters. 2013. Sep, 4(3): 41-46
Copyright ©2013, Korean Society Mass Spectrometry
  • Received : July 22, 2013
  • Accepted : September 24, 2013
  • Published : September 30, 2013
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About the Authors
Nusrat, Jahan
Department of Applied Biochemistry
Taeseong, Park
Division of Mass Spectrometry Research, Korea Basic Science Institute, Ochang 363-883, Korea
Young Hwan, Kim
Graduate School of Analytical Science and Technology, Chungnam National University, Daejeon 305-764, Korea
Dongsun, Lee
Department of Applied Biochemistry
Hackyoung, Kim
Department of Applied Biochemistry
Kwangmo, Noh
Nanotechnology Research Center, Konkuk University, Chung-ju 380-701, Korea
Young Jun, Kim
Nanotechnology Research Center, Konkuk University, Chung-ju 380-701, Korea

The goal of this study is to find an experimental condition which enables us to perform enzymatic studies on the cellular behavior of PTEN (phosphatase and tensine homolog) through identification of molecular species of phosphatidylinositol 3,4,5-trisphosphates and their quantitative analysis in a mammalian cell line using mass spectrometry. We initially exployed a two-step extraction process using HCl for extraction of phosphatidylinositol 3,4,5-trisphosphates from two mammalian cell lines and further analyzed the extracted phosphatidylinositol 3,4,5-trisphosphates using tandem mass spectrometry for the identification of them. We finally quantified the concentration of phosphatidylinositol 3,4,5-trisphosphates using internal standard calibration. From these observation, we found that HEK 293-T cells is a good model to examine the enzymatic behavior of PTEN in a cell, and the minimum amount of phosphatidylinositol 3,4,5-trisphosphates is more than 50 pmol for quantification in a mass spectrometer. These results suggest that the well-optimized experimental conditions are required for the investigation of the cellular PTEN in terms of the catalytic mechanism and further for the detailed identification of cellular substrates.
Phosphoinositides, the phosphorylated derivatives of phosphatidylinositol (PI) are negatively charged phospholipids. Phosphatidylinositol 3,4,5-trisphosphates, also known as PtdIns(3,4,5)P 3 s, PI(3,4,5)P 3 s or PIP 3 s among the phosphoinositides are the most difficult to characterize due to their presence in low concentration into cell. 1 - 3 Several evidences showed that PIP 3 s principally were accumulated into cell in response to a variety of stimuli, such as growth factors and oxidative stress, where phosphatidylinositol 4,5-disphosphates (PtdIns(4,5)P 2 s or PI(4,5)P 2 s) are phosphorylated at 3 position of the inositol ring by the action of PI3-Kinase. 4 - 8 PIP 3 s act as an important secondary messenger in incorporating multiple intracellular signaling pathways and in adjusting a large range of cellular activities. 2 , 4 , 5 PIP 3 s can activate the downstream signaling events, like cell motility, cell proliferation, cell growth and cell survival via recruiting downstream signaling molecules (PKB/Akt) containing pleckstrin homology (PH) domain. 9 , 10 Several studies showed that natural oncogenic form of PI3-Kinases caused elevation in PIP 3 levels, activation of Akt and tumor progression. 8 , 11 , 12
Some recent studies showed that PIP 3 s were degraded by the two inositol phosphatases, SHIP (SH2-containing inositol phosphatase, dephosphorylates PIP 3 at the 5 position to produce PI(3,4)-P 2 ) and PTEN (phosphatase and tensine homolog, hydrolyzes PIP 3 at the 3-position to produce PI(4,5-P 2 ). 5 , 13 , 14 PTEN (phosphatase and tensine homolog deleted on chromosome ten)/MMAC (mutated in multiple advanced cancers) is a tumor suppressor gene located at 10q23 15 , 16 , which encodes a 55 kDa protein composed of 403 amino acids. 13 , 15 , 16 PTEN protein contains the consensus motif of HCXXGXXR(S/T) found in all protein tyrosine phosphatases (PTPs). 5 Studies on tumor cell line showed that certain mutated PTEN induced elevated levels of PI(3,4,5)P 3 and of Akt activity 13 , 17 , 18 , and the introduction of wild type PTEN reduced levels of both. 18 , 19 In another study, it was found that PTEN inactivation by oxidative stress also caused an increase in cellular PtdIns(3,4,5)P 3 levels. 20
Recently, characterization of PIP 3 s has received great attention in the field of lipidomics due to their involvement in lipid related diseases. There are different methods to identify them in cell extracts including receptor displacement assays, metabolic labeling, and chromatographic separation of the radiolabeled products after deacylation, 6 , 21 - 23 but these techniques are technically demanding and suffer some limitations. Use of mass spectrometry based lipidomics can overcome these technical limitations and improve the detection process without previous separation through HPLC or TLC because of its high resolving power. Recently phosphatidylinositols were characterized in murine brain extracts using matrix-assisted laser desorption/ionization(MALDI)-time-of-flight(TOF)mass spectrometer(MS). 24 Use of electrospray ionization (ESI)-MS also reported for phosphatidylinositol monophosphates (PIPs) and phosphatidylinositol diphosphates (PIP 2 s) profiling in lipid extracts from cultured cells and rat brain 3 and for PIPs, PIP 2 s and PIP 3 s in murine macrophage extracts. 6
In the present study we searched experimental conditions to characterize molecular species of PIP 3 s upon expression of PTEN protein in HeLa and HEK 293-T cell lines by using mass spectrometry. We initially found that more than 50 pmol of PIP 3 s are required for quantitation of them in a mass spectrometry and HEK 293-T cell is proper for study of cellular PTEN on enzymatic behavior in a cell. We recognized that the level of most of PIP 3 s slightly reduced in HEK 293-T cells expressing of wild type PTEN protein and quantitatively increased in HEK-293T cells expressing of C124S mutant PTEN protein.
Experimental Section
- Chemicals and plasmid DNA
Media and reagents for cell culture were obtained from WelGENE Inc. (Daegu, Korea), transfection reagents (Lipofectamine™ LTX and PLUS™ Reagents) and OPTIMEM® I Reduced Serum Medium from Invitrogen (San Diego, CA, USA). HA-probe (Y-11) and PTEN (FL-403) antibodies used as primary antibody in western blot were purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA), BCA kits for protein concentration determination from Thermo Scientific. Standard phosphoinositides (PtdIns-(1,2-dipalmitoyl) (ammonium salt), PtdIns-(3)-P (1,2- dipalmitoyl) (ammonium salt), PtdIns-(4)-P (1,2-dipalmitoyl) (ammonium salt), PtdIns-(5)-P (1,2-dipalmitoyl) (ammonium salt), PtdIns-(3,5)-P 2 (1,2-dipalmitoyl) (sodium salt), PtdIns- (3,4)-P 2 (1,2-dipalmitoyl) (sodium salt), PtdIns-(4,5)-P 2 (1,2- dipalmitoyl) (sodium salt), and PtdIns-(3,4,5)-P 3 (1,2- dipalmitoyl) (sodium salt)) and internal standards (PtdIns- (3,4,5)-P 3 (1,2-dipalmitoyl)-d 62 (sodium salt)) were obtained from Cayman Chemical (Ann Arbor, MI, USA). Plasmid DNA pSG5L HA PTEN wt (ampR) and pSG5L HA PTEN C124S were purchased from Addgene (Cambridge, MA, USA).
- Cell culture and transfection
HeLa and HEK 293-T cells were cultured in DMEM containing 10% fetal bovine serum, 100 U/mL penicillin and 100 μg/mL streptomycin and maintained at 37℃ in a humidified atmosphere with 5% (v/v) CO 2 . For a transfection, cells were plated in a 10 cm cell culture dish 24 h before a transfection. When cells were 50% to 80% confluent, transfection was performed using Lipofectamine™ LTX and PLUS™ Reagents with Opti-MEM® I Reduced Serum Medium according to the manufacture’s instruction.
- Phosphoinositdes extraction
Phosphoinositides were extracted as described 1 , 3 , 6 and slightly modified. Sample (~10 7 cells of 2 days after transfection) was transferred into 15 mL polypropylene centrifuge tube. 3 mL of ice-cold chloroform/methanol (1:2) containing 5 ng of internal standard (PtdIns-(3,4,5)-P 3 (1,2- dipalmitoyl)-d 62 (sodium salt)) was added to centrifuged cell pellets. After vigorous vortexing, the sample was incubated on ice for 15 min. Ice-cold chloroform (1 mL) was added, followed by phase splitting buffer (1 mL of 1.76% KCl, 100 mM citric acid, 100 mM Na 2 HPO 4 , 5 mM EDTA, and 5 mM tetrabutyl ammonium hydrogen sulphate, pH 3.6) to induce a phase-split. After mixing, the sample was incubated on ice for 5 min. To complete the phase-split the sample was centrifuged (200 x g, 5 min). The lower, organic phase was transferred into a clean tube. The upper, aqueous phase was reextracted with 2 mL synthetic lower phase (150 μL of water, 2 mL of 0.25 M methanolic acid, 4 ml of chloroform, and 1.5 mL of phase splitting buffer) and centrifuged (200 x g, 5 min) and the resultant lower phase combined with the previous lower phase extract. 0.88% KCl (2 mL) was added to the remaining aqueous phase prior to extraction with 2 mL water-saturated butanol (30 min incubation on ice). The resultant butanol-rich upper phase was combined with the previous lower phase extracts. After drying, the sample was reextracted using 800 μL of chloroform/methanol (1:1) and 500 μL of 0.4% acetic acid. The solvent from the collected lower layer was evaporated in a vacuum centrifuge and resuspended in 50 μL of chloroform/methanol/isopropanol (with ammonium acetate 5mM) (1:2:4).
- Protein determination and western blot
Protein expression was analyzed by western blotting. A 10 cm culture dish of transfected cells was collected by centrifugation at 500 x g for 5 min, washed with phosphate buffered saline (PBS). After 30 min incubation at −80℃, the cells were lysed in RIPA buffer supplemented with protease inhibitor and phosphatase inhibitor cocktail 1 & 2 (Sigma Aldrich Korea), and then vortexed for 15 min, and cell lysates were centrifuged at 14,000 x g for 10 min to remove insoluble material. Protein concentration was determined by BCA assay. Protein samples were prepared by boiling lysates in reducing SDS-sample buffer for 5 min. Proteins were separated by 12.5% SDS-PAGE, and blotted to nitrocellulose transfer and immobilized membrane. The blotted membranes were blocked with 3% nonfat dry milk in TBS-T buffer (10 mM Tris, 150 mM NaCl, 0.2% Tween- 20, pH 8.0). The membrane was probed with an appropriate primary antibody for overnight at 4℃ and subsequently probed with secondary antibody for 1 h. Immunoreactive bands were visualized using a chemiluminescence kit from Amershan Bioscience Co. (Piscaraway, NJ, USA).
- Mass spectrometry
Mass spectral analysis was performed on SYNAPT® G2 High Definition MS™ System with Q-TOF technology (Waters Corporation, MA, USA). The instrument was equipped with NanoMate (Advion, NY, USA), as an electrospray source. Samples were analyzed at an infusion rate of 20 μL/min in negative ionization mode over the range of m/z 50-1,500. The ion spray voltage was set at −1.2 kV and the source temperature was 80℃. Data were collected with the MassLynx™ application managers (Waters Corporation MA, USA).
Results and Discussion
- PTEN expression on mammalian cells
The main target of this study is to measure quantitative variation of PIP 3 species which have different combination of fatty acid chain, among the wild type PTEN and mutant type PTEN expressing cells. In this regard we transfected HeLa and HEK 293-T cells with wild and mutant type (C124S) plasmid DNA each. To check the PTEN expression we performed western blotting probing with appropriate antibodies (HA and PTEN antibody) ( Figure 1 ). The western blot images in HeLa cells showed that wild type PTEN expressed a little less than C124S mutant PTEN and transfected PTEN was in a more amount than endogenous
PPT Slide
Lager Image
Western blot images of wild and mutant type PTEN expression in HeLa and HEK 293-T cell line. (a) Probed with HA antibody (HeLa cell), (b) Probed with PTEN antibody (HeLa cell), (c) Probed with HA antibody (HEK 293T cell line) and (d) Probed with PTEN antibody (HEK 293T cell line). C, control; WT, wild type; and MT, mutant type.
PTEN in both mutant and wild type expressing cells. The western blot images in HEK 293-T cells showed that both
PPT Slide
Lager Image
Mass spectrometric data of phosphoinositide standards (a) and general chemical structure of phosphoinositides, which is adapted from ref. 25 with slight modification (b).
wild type and C124S mutant PTEN expressed in a similar amount and endogenous PTEN was observed in a negligible amount. Based upon the different behavior of PTEN expression between HeLa and HEK 293-T cells, we thought that focusing on the lipidomic analysis of PIP 3 s in HEK 293- T cells is decent because observing quantitative variation of PIP 3 s needs measurement in a condition of the same amount of enzyme between wild type and active site mutant.
- Mass spectrometric analysis of phosphoinositide standards
To validate the sensitivity of the mass spectrometer in phosphoinositides’ detection, mass spectrometric analysis of phosphoinositide standards (PI, PIP, PIP 2 and PIP 3 ) with different concentration was performed ( Figure 2 (a)). The experiment showed the gradual increase of ion intensity of the phosphoinositide standards with their increased concentration. This suggests the lower limitation of detection of PIP 3 using the mass spectrometric condition was found to be ≥50 pmol for PIP 3 . Therefore, we found that required amount of PIP3s extracted from mammalian cells is at least 50 pmol in order to quantify molecular species of them. Based upon this observation, we checked the change of PIP 3 s’ amount
PPT Slide
Lager Image
Representative mass spectrum (a, b) and MS/MS analysis (c, d) of phosphoinositides extracted from (a) HeLa cell line and (b) HEK 293-T cell line. (c) PIP3 (34:1) was identified at m/z 1075.80 and (d) PIP3 (36:3) was identified at m/z 1099.81.
with different numbers of extracted cells (data not shown) and found that the minimum number of extracted cells is more than 10 7 so as to quantify the PIP 3 s. Additionally we provided general chemical structure of phosphoinositides in Figure 2 (b) for clear understanding of their mass spectrum.
- Mass spectrometric analyses of phosphoinositides extracted from mammalian cells
To verify the effect of transfected PTEN on cellular PIP 3 s, phosphoinositides’ were extracted from the transfected mammalian cell lines (HeLa cell and HEK 293-T cell) and subjected to the mass spectrometry analyses. We followed a 2 step extraction method of PIP 3 s from cell based on phase splitting using HCl. In order to confirm if PIP 3 s are extracted in a proper way, we checked recovery amount of PIP 3 with PIP 3 standard (50 pmol) through extraction process of this experiment and found that more 95% of PIP 3 standard was recovered through comparing the intensity of it in a mass spectrum before extraction and after extraction (data not shown). Relatively higher numbers of mass peaks were observed in mass spectrum of PIPs extracted from HeLa cell ( Figure 3 (a)) than them extracted from HEK 293-T cell ( Figure 3 (b)) due to more complex composition of extracted lipids in HeLa cell line. We tried to identify PIP 3 s from this mass spectrum through MS/MS analysis, and found that a certain number of PIP 3 s which further were quantified through internal standard calibration. MS/MS analysis was performed so as to confirm identity and fatty acid composition of PIP 3 s. MS/MS spectra ( Figure 3 . (c) and (d)) of PIP 3 (34:1) and PIP 3 (36:3) among them of identified PIP 3 s were representatively presented here. MS/MS analysis of the precursor ion peak at m/z 1075.80 was visibly assigned as PIP 3 (34:1). Two characterized fragments of the polar head group appeared at m/z 241.00 (inositolphosphate-H 2 O) and m/z 96.96, which is from the [H 2 PO 4 ] anion and one fragment of glycerol part was found at m/z 153.00 (glycerophosphate-H 2 O). Two fatty acid fragments were identified at m/z 281.20, which corresponds to oleic acid 18:1, and at m/z 255.20, which corresponds to palmitic acid 16:0. Another characteristic phosphoinositide PIP 3 (36:3) was identified at m/z 1099.82. Three characterized fragments from polar head group and glycerol part were appeared as above. Two fatty acid fragments were identified at m/z 281.20, which corresponds to oleic acid 18:1, and at m/z 279.20, which corresponds to linoleic acid 18:2.
- Quantitative analysis of PIP3s
Quantitative study of the identified PIP 3 s using a PIP 3 internal standard showed the concentration of PIP 3 s obtained from both HeLa and HEK 293-T cell in ng of lipid/mg of protein. We identified and quantified 7 PIP 3 s from both HeLa and HEK 293-T cell ( Table 1 ). In case of HeLa cell, PIP 3 (34:1) and PIP 3 (32:0) were found in a higher concentration than other PIP 3 s, and the effect of both
Identified phosphatidylinositol 3,4,5-trisphosphates in HeLa and HEK 293-T cell line upon PTEN expression.a: ng of lipid/mg of protein, represents average ± standard deviation from triplicate experiments
PPT Slide
Lager Image
Identified phosphatidylinositol 3,4,5-trisphosphates in HeLa and HEK 293-T cell line upon PTEN expression. a: ng of lipid/mg of protein, represents average ± standard deviation from triplicate experiments
wild type and mutant PTEN expression showed strangely increasing concentration of all PIP 3 s except PIP 3 (34:1). This strange behavior might be originated from difficult interference of endogenous PTEN behavior due to complicate circumstance of HeLa cell. In case of HEK 293-T cell, PIP 3 (32:0) was found in a higher concentration that other PIP 3 s, and the concentrations of identified PIP 3 s were higher in mutant type than wild type expressing cells since the functionally active PTEN can convert PIP 3 to PIP 2 by dephosphorylating at 3 position of the inositol head. Therefore, we conclude that HEK 293-T cell line is an appropriate system to study enzymatic behaviors of PTEN in a cell.
In conclusion, we found that in order to enzymatically study cellular activity of PTEN through mass spectrometry the extracted amount of PIP 3 s should be more than 50 pmol, which is extracted from more than 10 7 mammalian cells. Additionally, we found that HEK 293-T cell is proper to see enzymatic manner of PTEN in a cell. These results suggest that several experimentally optimized conditions are required for investigation of cellular PTEN on a catalytic mechanism and a detailed identification of cellular substrates. We will further investigate on more detailed identification of molecular species of cellular PIP 3 s based upon PTEN enzymatic activity in HEK 293-T cells with these optimized conditions and more experiments. In addition, we will study quantitative change of PIP 3 s with differently expressed levels of PTEN in mammalian cells obtained through inducible expression system for kinetic study of cellular PTEN.
This work was supported by the Basic Science Research Program (2010-0002609) through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science, and Technology and by the Visiting Researcher Program in 2011 of Korea Basic Science Institute.
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