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The protein phosphatase activity of PTEN is essential for regulating neural stem cell differentiation
Molecular Brain volume 8, Article number: 26 (2015)
The tumor suppressor gene Phosphatase and tensin homolog (PTEN) is highly expressed in neural progenitor cells (NPCs) and plays an important role in development of the central nervous system. As a dual-specificity phosphatase, the loss of PTEN phosphatase activity has been linked to various diseases.
Here we report that the protein phosphatase activity of Pten is critical for regulating differentiation of neural progenitor cells. First we found that deletion of Pten promotes neuronal differentiation. To determine whether the protein or lipid phosphatase activity is required for regulating neuronal differentiation, we generated phosphatase domain-specific Pten mutations. Interestingly, only expression of protein phosphatase-deficient mutant Y138L could mimic the effect of knocking down Pten, suggesting the protein phosphatase of Pten is critical for regulating NPC differentiation. Importantly, we showed that the wild-type and lipid phosphatase mutant (G129E) forms of Pten are able to rescue neuronal differentiation in Pten knockout NPCs, but mutants containing protein phosphatase mutant cannot. We further found that Pten-dependent dephosphorylation of CREB is critical for neuronal differentiation.
Our data indicate that the protein phosphatase activity of PTEN is critical for regulating differentiation of NSCs during cortical development.
Embryonic neural stem cells (NSCs) self-renew and also differentiate into neurons, astrocytes, and oligodendrocytes ; maintaining a balance between these two processes is essential for normal brain development [2,3], and requires the coordinate regulation of multiple signaling pathways .
Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) is a tumor suppressor and autism-related gene that regulates proliferation and differentiation in a variety of cell types [5-8]. As a dual-specificity phosphatase, the PTEN protein contains catalytic and C2 domains and a C-terminal PDZ-binding motif . The lipid phosphatase activity is required for antagonizing the phosphatidylinositol 3-kinase (PI3K)/AKT pathway, which controls cell proliferation and survival [10-13]; the major PTEN substrates are cyclic AMP response element-binding protein  and PTEN itself .
The complete inactivation of PTEN can lead to seizures, highlighting its importance in normal brain function. The G129E mutation, observed in Cowden syndrome, specifically abolishes the lipid phosphatase activity , while the Y138L mutation results in the loss of protein phosphatase function . Embryonic Pten null mice have enlarged brains [7,8,18], while Pten deletion in adult mice enhanced NSC proliferation and differentiation into neurons, suppressed cell death, and resulted in an increased cell size [5-8]. Despite these observations, the Pten deletion mouse model has not provided a clear insight into the role or mechanism of PTEN function in NSCs during embryonic development.
The present study investigated whether the catalytic activity of PTEN is involved in NSC differentiation in embryos. Using NSC-derived neurosphere cultures transduced with lentivirus expressing mutant protein, it was found that the protein phosphatase activity is specifically required for balancing NSCs fate determination.
Pten-deficient NSCs differentiate precociously into neurons
To evaluate the function of Pten in embryonic NSCs, the fate of neurospheres derived from Pten loxP/loxP embryos at E12.5 and maintained under proliferating culture conditions was examined. We first isolated neural stem cells from mouse brain at E12.5 and stained with neural progenitor marker Nestin and found that majority of neural stem cells were Nestin positive cells (Additional file 1: Figure S1A). After five days, neurospheres were infected with lentivirus expressing GFP (control) or Cre-GFP (for Pten deletion), and cells were induced to differentiate as described in section 2.2. After 4–5 days, there was no PTEN protein expressed by NSCs transduced with Cre-GFP (Figure 1A). Cells were examined the expression of the differentiated neuron marker Tuj1 (Figure 1B). The number of Tuj1+GFP+ cells was 53.2% higher in PTEN-deficient cells than controls (11.9 ± 1.4 vs. 7.8 ± 1.6; P < 0.01) (Figure 1C).
We further examined whether deletion of Pten may affect the proliferation of neural stem cells. Indeed, we found that deletion of Pten leads to a significant increase of diameter of neurospheres, comparing to GFP only virus infections (Figure 1D, E). We also stained neural stem cells with Caspase3 and found that there was not significant neuronal cell death when Pten was knockout (Additional file 1: Figure S1B). To address whether Pten deletion would affect glial differentiation, we examined the glia cells by staining GFAP in NSCs under differentiation condition with or without Pten deletion. We found that Pten deletion did not affect GFAP-positive cell numbers (Additional file 2: Figure S2A, B). We speculate that in our preparation and culture conditions, NSCs preferred to undergo neuronal differentiation rather than glial differentiation. Neither we found that PTEN lipid and protein phosphatase activity show effect on the glial differentiation (Additional file 3: Figure S3).
To determine whether PTEN-deficient neurons are able to develop normally, we stained neuronal marker MAP-2 and NeuN on the neurons cultured over 14–17 days after neuronal differentiation and found that PTEN-deficient neurons were still able to differentiate into mature neurons (Additional file 4: Figure S4A, B). Interestingly, we found that the total neurite length is significantly increased when Pten was deleted, in consistent with previous finding that Pten is critical for neuronal dendritic growth (Additional file 5: Figure S5A,B). Thus we think that the increase of neurite growth after Pten deletion in our experiments echo this previous finding that loss of Pten lead to increased dendritic length by regulating Akt/mTOR/S6K pathway.
PTEN protein phosphatase activity maintains NSCs in a progenitor state
To evaluate the mechanism underlying the observed effects of PTEN in NSC differentiation, WT or mutant PTEN—harboring a loss-of-function mutation in either the protein (Y138L) or lipid (G129E) phosphatase domain, or both (C124S)—or PTEN shRNA was overexpressed in NSCs. PTEN protein expression was absent in PTEN RNAi cells (Figure 2A). A 55 kDa band was observed upon lentiviral transduction of NSCs with WT, Y138L, G129E, and C124S, corresponding to the PTEN protein (Figure 2B). NSCs were infected with lentivirus expressing GFP, PTEN shRNA, or WT, Y138L, G129E, or C124S (Figure 2C). There was no difference in the number of Tuj1+ neurons upon infection of cells with GFP control, WT, G129E, or C124S constructs. However, an increase in neuronal production was observed upon overexpression of Y138L (10.0 ± 0.9 vs. 7.48 ± 0.6 in GFP controls; P < 0.001), 34.2% more than for PTEN WT overexpression (10.0 ± 0.9 vs. 7.48 ± 1.1; P < 0.05) (Figure 2D).
To further confirm this result, we made RNAi-resistant rescue constructs of wild-type, G129E, and Y138L mutant of PTEN (Figure 3A, B). In experiments described above, we found that shRNA-resistant HA-PTEN WT, shRNA-resistant HA-PTEN G129E rescued the effect of PTEN shRNA (Figure 3A-D). Surprisingly, an increase in neuronal production was still observed upon shRNA-resistant HA-PTEN Y138L (Figure 3C, D). The results of this experiment provide further evidence that PTEN protein phosphatase is critical for neuronal differentiation in embryonic NSCs.
Expression of WT PTEN rescues the precocious differentiation induced by inactivation of PTEN protein phosphatase function
To confirm that the protein phosphatase activity of PTEN mediates NSC differentiation, Pten loxP/loxP NSCs were co-transduced with Cre-GFP and GFP, WT PTEN, Y138L, G129E, or C124S constructs (Figure 4A). Overexpression of WT PTEN abolished the increase in the number of Tuj1+ cells induced by the loss of PTEN (12.9 ± 0.3 vs. 10.3 ± 3.0 for GFP only; P = 0.13), while this was not observed when the GFP control lentivirus was co-infected with Cre-GFP (Figure 4B). G129E, which retains protein phosphatase activity, also rescued the excessive differentiation induced by PTEN deficiency (13.6 ± 1.1 Tuj1+ cells vs. 10.3 ± 3.0 for GFP only; P = 0.09).
Previous studies have shown that PTEN is required for the physiological function of NSCs, and PTEN ablation in the mouse cortex and hippocampus leads to macrocephaly, social behavior and learning deficits, seizures, and increased anxiety [5,8,18]. More recently, increased proliferation and differentiation rates have been observed in Pten-deficient adult NSCs, leading to the production of hypertrophic neurons and ultimately to the early depletion of the NSCs pool. In Pten mutant mice, NSCs in the hippocampus preferentially differentiated into astrocytes rather than neurons [6,7]. In accordance with effects observed in adult NSCs , the results of present study provide evidences for increased neuronal differentiation in embryonic NSCs upon loss of PTEN.
PTEN-dependent CREB dephosphorylation is critical for neural stem cell differentiation
It is reported that PTEN dephosphorylated CREB directly through its protein phosphatase activity . Indeed, we confirmed that the CREB phosphorylation significantly increased in PTEN-depleted neurons by RNAi, indicating PTEN also dephosphorylate CREB protein at S133 site in NSCs and mouse neurons (Figure 5B). Next we would like to examine whether CREB is required for PTEN-regulated neural differentiation. We overexpressed wild-type and phosphorylation mutant S133A form of CREB after knocking down PTEN (Figure 5A, C). Interestingly, we found that wild-type CREB, but not S133A mutant, could rescue the abnormal neuronal differentiation caused by PTEN deletion, suggesting that PTEN may regulate neuronal differentiation through dephosphorylating CREB at S133 site (Figure 5A, C).
The loss of PTEN phosphatase activity has been linked to various diseases. For instance, PTEN G129E was identified in two families with Cowden disease . In glioblastoma cells, PTEN lipid and protein phosphatase activities independently inhibit cell proliferation, and both are coordinately required to effectively inhibit cell invasion . The protein but not the lipid phosphatase activity is involved in the decrease in dendritic spine density of neurons overexpressing wild-type PTEN . Here it was shown that NSC maintenance is abolished when the protein phosphatase domain of PTEN is inactivated, leading to accelerated neuronal differentiation. This activity may be self-directed (i.e., via dephosphorylation of PTEN) , and is likely distinct from its role in the PI3K/AKT pathway, which is antagonized by PTEN lipid phosphatase activity and regulates cell proliferation, survival, and motility . Moreover, several reports have highlighted the link between PTEN protein phosphatase activity and the regulation of cell migration and invasion .
In summary, the findings of this study demonstrate that PTEN deficiency promotes neurogenesis in embryonic NSCs, and the protein phosphatase activity of PTEN is specifically required to maintain NSCs in a self-renewing state during embryonic development. Additional experiments are required to determine if there are other substrates targeted by PTEN-mediated dephosphorylation in the differentiation of the NSC population during embryonic development.
Materials and methods
Pten loxP/loxP mice were purchased from the Jackson Laboratory (Farmington, CT, USA). All experimental procedures were performed according to the guidelines and under the approval of the Animal Care and Use Committee of the Institute of Neuroscience of the Chinese Academy of Sciences.
Neurosphere cultures and lentivirial transduction
NSCs were obtained from mice at embryonic day (E)12.5. Briefly, the cortex was dissected and placed in ice-cold phosphate-buffered saline (PBS; Invitrogen); the tissue was triturated, then passed through a 70-μm nylon cell strainer (BD Biosciences, Franklin Lakes, NJ, USA) to dissociate the cells, which were plated at 2 × 105 cells/ml in Dulbecco’s Modified Eagle’s Medium (DMEM)/F12 medium with 2% B27 supplement without vitamin A, 1% N2 supplements, and 10 ng/ml each of recombinant human basic fibroblast growth factor (bFGF) and epidermal growth factor (EGF; all from Invitrogen, Carlsbad, CA, USA). Neurospheres were passaged every five days. To induce NSC differentiation, resuspended cells were plated in poly-l-ornithine-coated wells of an 8-well chambered slide (Nunc Lab-Tek II; Thermo Fisher Scientific, Waltham, MA, USA) at a density of 5 × 104 cells/well in the same supplemented DMEM/F12 medium, but with 1% fetal bovine serum (Invitrogen) and without growth factors. Lentiviruses (108–9 vg/ml) were tansduced in a single-cell suspension. Cells were allowed to differentiate for five days. For measuring the size of neurospheres, the NSCs were transfected with lentivirus expressing GFP or CreGFP at Day 1. At Day 3, GFP positive cells were collected by flow cytometry. The GFP positive cells were cultured at a density of 5000 cells/well in a 6-well plate. At day 6, the neurospheres were pictured and the sizes were measured.
Cells were fixed in 4% paraformaldehyde in PBS. After washing in PBS, cells were blocked in blocking buffer (3% bovine serum albumin and 0.2% Triton X-100 in PBS), then incubated with primary and secondary antibodies diluted in blocking buffer. Cell nuclei were stained with DAPI. The following primary antibodies were used: goat α-green fluorescent protein (GFP; 1:500; Millipore, Billerica, MA, USA), rabbit α-Tuj1 (1:1,000; Invitrogen), goat α-HA (1:1,000; Millipore), and mouse α-GFP (1:2,000; Millipore), chicken α-GFAP (1:1000; Abcam, Cambridge, UK), mouse α-nestin (1:1000; R&D system), mouse α-MAP-2(1:500, Millipore), rabbit α-NeuN(1:1000, Miliipore).
Total protein was extracted from NSCs cultured samples in RIPA buffer using a standard protocol. Samples were resolved by 8% SDS-PAGE and transferred to a polyvinylidene fluoride membrane (Millipore). Membranes were probed with the following primary antibodies: α-PTEN (1:1000; Cell Signaling Technology, Danvers, MA, USA), α-HA (1:2500; Abmart, Arlington, MA, USA), α-CREB (1:1000; Cell Signaling Technology, Danvers, MA, USA), α-p-CREB(S133) (1:1000; Cell Signaling Technology, Danvers, MA, USA) and α-glyceraldehyde 3-phosphate dehydrogenase (GAPDH; 1:5000; Abcam, Cambridge, UK), followed by incubation with a horseradish peroxidase-conjugated secondary antibody and processing with an enhanced chemiluminescence kit (Thermo Fisher Scientific).
The RNAi targeting sequence for mouse Pten was 5′-AGA CAA GGC CAA CCG ATAC-3′. The wild-type (WT) Pten overexpression construct was generated by subcloning the ORF with an HA tag between the BamHI and EcoRI sites of the FUGW vector (Addgene). For the replacement construct, the Pten shRNA sequence was inserted into the PacI site of the expression vector under the control of H1 promoter. The following forward and reverse primer pairs were used to generate the PTEN mutation constructs: C124S, 5′-TCA TGT TGC AGC AAT TCA CTC T-3′ and 5′-CCG TCC CTT TCC AGC TTT-3′; G129E, 5′-ACT GTA AAG CTG GAA AGG AA-3′ and 5′-CAC AAA TCA TTA CAC CAG TCC G-3′; Y138L, 5′-CTC TTA TTG CAT CGG GGC AAA TTT TTA AA-3′ and 5′-AAT TTG CCC CGA TGC AAT AA-3′. The shRNA-resistant HA-PTEN was generated by introduction of six silent mutations into the sequence of Pten targeted by the shRNA, indicated in the following by lower case letters: 5′-GAt AAa GCt AAt aGg TAC-3′.
For counting percentage of differentiated cells, five images/sections were acquired randomly under a 10х object lens, immunolabeled cells were counted manually. Over 800 cells were counted per group from each experiment. For measurement of total neurite length, the images were obtained under a 40х object lens. The lengths of 30 neurons in each experimental group were measured from 4 independent experiments. All the data were measured using Image J.
All results were expressed as mean ± SD and were analyzed using Stata v. 10 software (Stata Corporation, College Station, TX USA). A two-sample t test with equal variance was used to compare results from each group. A P value < 0.05 was considered statistically significant.
Basic fibroblast growth factor
Epidermal growth factor
Green fluorescent protein
Neural stem cells
Phosphatase and tensin homolog deleted on chromosome 10
CAMP response element-binding protein
Gage FH. Mammalian neural stem cells. Science. 2000;287:1433–8.
El SR, Huisman MA, Lowik CW, Frijns JH. Uncomplicated differentiation of stem cells into bipolar neurons and myelinating glia. Biochem Biophys Res Commun. 2008;376:358–62.
Svendsen CN, Bhattacharyya A, Tai YT. Neurons from stem cells: preventing an identity crisis. Nat Rev Neurosci. 2001;2:831–4.
Molofsky AV, Pardal R, Morrison SJ. Diverse mechanisms regulate stem cell self-renewal. Curr Opin Cell Biol. 2004;16:700–7.
Gregorian C, Nakashima J, Le Belle J, Ohab J, Kim R, Liu A, et al. Pten deletion in adult neural stem/progenitor cells enhances constitutive neurogenesis. J Neurosci. 2009;29:1874–86.
Bonaguidi MA, Wheeler MA, Shapiro JS, Stadel RP, Sun GJ, Ming GL, et al. In vivo clonal analysis reveals self-renewing and multipotent adult neural stem cell characteristics. Cell. 2011;145:1142–55.
Amiri A, Cho W, Zhou J, Birnbaum SG, Sinton CM, McKay RM, et al. Pten deletion in adult hippocampal neural stem/progenitor cells causes cellular abnormalities and alters neurogenesis. J Neurosci. 2012;32:5880–90.
Groszer M, Erickson R, Scripture-Adams DD, Lesche R, Trumpp A, Zack JA, et al. Negative regulation of neural stem/progenitor cell proliferation by the Pten tumor suppressor gene in vivo. Science. 2001;294:2186–9.
Waite KA, Eng C. Protean PTEN: form and function. Am J Hum Genet. 2002;70:829–44.
Zhang QG, Wu DN, Han D, Zhang GY. Critical role of PTEN in the coupling between PI3K/Akt and JNK1/2 signaling in ischemic brain injury. FEBS Lett. 2007;581:495–505.
Zhao H, Sapolsky RM, Steinberg GK. Phosphoinositide-3-kinase/akt survival signal pathways are implicated in neuronal survival after stroke. Mol Neurobiol. 2006;34:249–70.
Salmena L, Carracedo A, Pandolfi PP. Tenets of PTEN tumor suppression. Cell. 2008;133:403–14.
Zhang QG, Wang XT, Han D, Yin XH, Zhang GY, Xu TL. Akt inhibits MLK3/JNK3 signaling by inactivating Rac1: a protective mechanism against ischemic brain injury. J Neurochem. 2006;98:1886–98.
Gu T, Zhang Z, Wang J, Guo J, Shen WH, Yin Y. CREB is a novel nuclear target of PTEN phosphatase. Cancer Res. 2011;71:2821–5.
Zhang XC, Piccini A, Myers MP, Van Aelst L, Tonks NK. Functional analysis of the protein phosphatase activity of PTEN. Biochem J. 2012;444:457–64.
Myers MP, Pass I, Batty IH, Van der Kaay J, Stolarov JP, Hemmings BA, et al. The lipid phosphatase activity of PTEN is critical for its tumor supressor function. Proc Natl Acad Sci U S A. 1998;95:13513–8.
Davidson L, Maccario H, Perera NM, Yang X, Spinelli L, Tibarewal P, et al. Suppression of cellular proliferation and invasion by the concerted lipid and protein phosphatase activities of PTEN. Oncogene. 2010;29:687–97.
Kwon CH, Luikart BW, Powell CM, Zhou J, Matheny SA, Zhang W, et al. Pten regulates neuronal arborization and social interaction in mice. Neuron. 2006;50:377–88.
Liaw D, Marsh DJ, Li J, Dahia PL, Wang SI, Zheng Z, et al. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat Genet. 1997;16:64–7.
Tibarewal P, Zilidis G, Spinelli L, Schurch N, Maccario H, Gray A, et al. PTEN protein phosphatase activity correlates with control of gene expression and invasion, a tumor-suppressing phenotype, but not with AKT activity. Sci Signal. 2012;5:a18.
This work has been supported by grants from the National Natural Science Foundation of China (no. 91232712, 81070519); Scientific Research Foundation of the Graduate School of Fudan University; and the Scientific Research Foundation of Shanghai Medical School of Fudan University
The authors declare that they have no competing interests.
JL, QZ and WZ drafted the manuscript. JL conceived the study, carried out western blotting, immunofluorescence, cell culture, plasmid construction, and statistical analysis. XY, LH and TC participated in the western blotting, plasmid construction, and cell counting. JZ and GC participated in the cell counting and statistical analysis. CC participated in the plasmid construction. ZC conceived of the study and participated in its design. All authors read and approved final manuscript.
Typical neurosphere and cell death detection. (A) Neurosphere after 5 days culture was shown by nestin staining (red). (B) Rarely cell death (Caspase 3 positive cells) was observed in differentiated cells after GFP or CreGFP lentivirus transfection.
PTEN deletion in NSCs has no effect on differentiation of glial cells. (A) The fate change of differentiated NSCs was ascertained by labeling with an antibody against the astrocyte marker GFAP. GFP+ cells represent the cells transfected with lentivirus. Nuclei were stained with DAPI. Scale bar = 40 μm. (B) No significant changes on GFAP+GFP+ cells was observed upon Pten deletion compared to Pten loxP/loxP controls. Data are expressed as mean ± SD. (n > 800 cells per group from each experiment).
PTEN lipid and protein phosphatase activity shows no effect on the glial differentiation of NSCs. (A) The fate change of differentiated NSCs was ascertained by labeling with an antibody against the astrocyte marker GFAP. GFP+ cells represent the cells transfected with lentivirus. Nuclei were stained with DAPI. Scale bar = 40 μm. (B) No significant changes on GFAP positive cells after each PTEN mutant overexpression were observed. Data are expressed as mean ± SD. (n > 800 cells per group from each experiment).
Neurons, differentiated from NSCs, develop into mature neurons. (A-B) Cells differentiated from NSCs 10 days after GFP or CreGFP lentivirus transfectionwere labeled with mature neuronal markers MAP2 and NeuN. Scale bar = 40 μm.
Total neurite length of control and Pten −/− neurons. (A) Representative image of neurite growth of differentiated neurons at 5 days after transfectionwith GFP or CreGFP lentivirus. Scale bar = 40 μm (B) The quantification plot of neurite length of differentiated neurons. Transfection with lentivirus expressing CreGFP showed a remarkable increase in neurite length compared to control.
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Lyu, J., Yu, X., He, L. et al. The protein phosphatase activity of PTEN is essential for regulating neural stem cell differentiation. Mol Brain 8, 26 (2015). https://doi.org/10.1186/s13041-015-0114-1
- Protein phosphatase activity
- Neural stem cells