- Research Article
- Open Access
The Nedd4-binding protein 3 (N4BP3) is crucial for axonal and dendritic branching in developing neurons
© Schmeisser et al.; licensee BioMed Central Ltd. 2013
- Received: 4 April 2013
- Accepted: 28 August 2013
- Published: 17 September 2013
Circuit formation in the nervous system essentially relies on the proper development of neurons and their processes. In this context, the ubiquitin ligase Nedd4 is a crucial modulator of axonal and dendritic branching.
Herein we characterize the Nedd4-binding protein 3 (N4BP3), a Fezzin family member, during nerve cell development. In developing rat primary hippocampal neurons, endogenous N4BP3 localizes to neuronal processes, including axons and dendrites. Transient in vitro knockdown of N4BP3 in hippocampal cultures during neuritogenesis results in impaired branching of axons and dendrites. In line with these findings, in vivo knockdown of n4bp3 in Xenopus laevis embryos results in severe alteration of cranial nerve branching.
We introduce N4BP3 as a novel molecular element for the correct branching of neurites in developing neurons and propose a central role for an N4BP3-Nedd4 complex in neurite branching and circuit formation.
- Xenopus laevis
Depending on the pattern and extent of how axons and dendrites undergo branching, a neuron has the ability to regulate the level of wiring and the strength of synaptic circuits. In this context, the ubiquitin proteasome system (UPS) has emerged as a decisive regulatory pathway[1–12]. Accumulating data underline the fact that Nedd4 (neural precursor cell expressed and developmentally downregulated), a HECT (homologous to E6-AP carboxyl terminus) domain ubiquitin ligase, is of special importance for neuronal network formation because of its capacity to regulate the growth and arborization of both dendrites and axons[14–18]. In the murine brain, for example, Nedd4 turns down Ras-related protein 2A (Rap2A) function, thus inhibiting Rap2 effector kinases of the Traf2- and Nck-interacting kinase (TINK) family and thereby promoting dendritic growth and arborization. Nedd4 was further shown to promote phosphatidylinositol 3-kinase (PI3K)-induced cytoskeletal rearrangements via UPS-mediated downregulation of the Nedd4 substrate phosphatase and tensin homolog (PTEN) to generate a terminally branched arbor in axons of Xenopus laevis retinal ganglion cells (RGCs). The same Nedd4-dependent regulatory mechanism was recently confirmed in axons of dorsal root ganglion (DRG) sensory neurons in the peripheral nervous system. In line with these findings, phrenic nerve fasciculation is severely disrupted in Nedd4-null mutants during embryonic development in vivo. Interestingly, various Nedd4-interacting proteins serving as accessory and/or adaptor molecules to recruit, sequester or modify Nedd4 have been identified in recent years[20, 21]. One of these potential adaptor proteins is the Nedd4-binding protein 3 (N4BP3). It was originally isolated as an interaction partner of Nedd4 in a yeast two-hybrid screen. On the basis of in vitro assays, the authors of that study subsequently identified the consensus PY motif (PPxY) in N4BP3 as the binding module for Nedd4, demonstrated that N4BP3 and Nedd4 colocalize in cytoplasmic vesicles and revealed that N4BP3 is not a ubiquitylation substrate of Nedd4.
In our present study, we show that N4BP3 is present in early neurites, growth cones, axons and dendrites of developing primary hippocampal neurons. We subsequently demonstrate that in vitro knockdown (KD) of N4BP3 in hippocampal cultures leads to impaired axonal and dendritic branching. We extend these findings in vivo by morpholino oligonucleotide (MO)-mediated KD of n4bp3 in developing X. laevis embryos, which results in abnormal branching of cranial nerves. On the basis of these findings, we propose that N4BP3 is essential for proper nerve cell development.
Nedd4-binding protein 3, a novel Fezzin family member
Nedd4-binding protein 3 is enriched in growth cones, axons and dendrites of developing hippocampal neurons
Knockdown of Nedd4-binding protein 3 in developing primary hippocampal cultures alters axonal and dendritic branching
n4bp3 is essential for cranial nerve branching in developing Xenopus laevis embryos
To investigate n4bp3 function in vivo, we made use of X. laevis as a model organism. First, we were interested in whether n4bp3 is expressed in the developing nervous system of X. laevis and investigated its expression profile during early embryogenesis by whole-mount in situ hybridization (WMISH) experiments using a specific antisense n4bp3 RNA probe. We found that n4bp3 transcripts are indeed detectable in developing brain structures, eyes, otic vesicles, heart, pronephros, liver and diverse cranial ganglia of X. laevis embryos (Figure 4A, Additional file2: Figure S2). The specific expression of n4bp3 in cranial nerves strongly argues for a role of n4bp3 during cranial ganglia development. To investigate this hypothesis, we designed an antisense MO based on the published X. tropicalis sequence [Xenbase:XM_002936850]. To test whether n4bp3 MO binds to its binding site, we cloned the n4bp3 MO binding site in front of and in frame with GFP (n4bp3 MO-GFP). Next, we injected the RNA of n4bp3 MO-GFP, together with either the control or n4bp3 MO. Coinjection of n4bp3 MO-GFP and the control MO led to GFP fluorescence, whereas embryos coinjected with n4bp3 MO-GFP, together with n4bp3 MO, showed no GFP fluorescence (Figure 4B). To test the specificity of n4bp3 MO, we injected the n4bp3 MO bilaterally into two-cell stage embryos, cultivated them until stage 15 and performed Western blot analysis to determine protein levels. Upon n4bp3 depletion, we found that n4bp3 protein level had strongly decreased compared to the wild type (WT) (Figure 4C).
Next, we injected n4bp3 MO into one animal dorsal blastomere of eight-cell stage X. laevis embryos to target anterior neural tissue, including developing cranial ganglia. As controls, we used either uninjected (WT) or control MO-injected embryos. At stage 46, we performed immunostaining experiments with the neurofilament-specific antibody 3A10 to detect cranial nerves using uninjected and MO-injected X. laevis embryos. Unilateral loss of n4bp3 function resulted in abnormal cranial ganglia development, including shorter, and even absent, ganglia, as well as reduced cranial nerve arborization at the injected site (Figure 4D and4E). In addition, significantly fewer arborization points were counted upon loss of n4bp3 (Figure 4F and4G). The control MO-injected or uninjected embryos revealed no changes in cranial nerve formation. These in vivo data strongly support our findings in primary hippocampal cultures showing disturbed branching of axons and dendrites upon loss of N4BP3 function.
Ubiquitylation plays a decisive regulatory role during the establishment of neural polarity, neuritogenesis and synapse formation[11, 12]. In this context, the ubiquitin ligase Nedd4 has emerged to be a crucial modulator. Previous studies have shown that Nedd4 is able to control axon arborization, dendrite branching and synaptic transmission[15, 16, 29, 30]. However, its molecular interactions, its regulation and its functions in neurons are still far from being completely understood. We have therefore started to uncover the functional role of N4BP3 in the developing nervous system. This hitherto uncharacterized protein not only contains a central Nedd4-binding motif but also exhibits a C-terminal Fez1 domain. This feature classifies N4BP3 as a member of the Fezzin family, a group of molecules that interacts with spine-associated Rap GTPase-activating proteins and the ProSAP/Shank platform in the postsynaptic density (PSD) of excitatory synapses via Fez1 and/or PDZ domain interaction, respectively[23–25]. However, N4BP3 exhibits the least conserved Fez1 domain among family members (see public databases such as NCBI) and contains only a rudimentary PDZ domain-binding motif. Therefore, N4BP3 might not exhibit its major functions within the PSD scaffold, as do other Fezzins. In fact, the presence of N4BP3 in neuronal processes, including axons and dendrites, implicates a role for this protein in early neuronal development. These observations are in line with the results of previous studies showing that N4BP3 interaction partner Nedd4 is also found in axons and growth cones of RGCs, as well as in neurites and growth cones of DRG sensory neurons. N4PB3 thus not only binds Nedd4 but also might have an impact on Nedd4-related processes in developing neurons. To test this hypothesis, we used an RNAi approach to transiently knock down N4PB3 and first conducted this experiment during the period of axonal branching of hippocampal neurons in culture. The resulting phenotype, a loss of predominantly secondary and tertiary branches and a significantly decreased ACI, does in fact resemble the Nedd4-KD phenotype in axons[15, 18]. Because Nedd4 is crucial not only for axonal branching but also for dendritic branching, we used the same approach used previously and transiently knocked down N4BP3 during the core period of dendritic branching in hippocampal cultures. Our subsequent analyses demonstrate that loss of N4BP3 leads to a less complex dendritic arbor. These data resemble the phenotypical alterations of Nedd4 deficiency on dendrites as described previously. Most interestingly, the Nedd4-binding motif in N4BP3 is conserved among species, including X. laevis. We reveal highly specific expression of n4bp3 in the X. laevis nervous system, including cranial nerve ganglia. Strikingly, loss of n4bp3 via MO-mediated KD severely disrupts cranial nerve development in X. laevis embryos in vivo. These results provide strong support for previous work in Nedd4-deficient mice, which exhibit a failure in caliber, growth, fasciculation and axon number of the phrenic nerve early in development.
On the basis of our loss of function studies in vitro and in vivo, we conclude that N4BP3 is essential for the proper development of neuronal processes among species. We further propose that N4BP3 could be crucial for Nedd4-related function during neural development. At this stage, however, two aspects are still unclear: (1) the molecular mechanism, that is, how N4BP3 might influence Nedd4 function; and 2) the consequences that a potential N4BP3-Nedd4 interplay in neurons have on Nedd4 substrates. In axons, for example, Nedd4 has repeatedly been shown to promote arborization via ubiquitylation of PTEN[15, 18], a central inhibitor of PI3K signaling and cytoskeletal growth[33, 34]. Moreover, Nedd4 is known to promote dendritic branching via ubiquitylation of Rap2, a negative regulator of dendrite growth. Based on the aforementioned facts, in future studies, it will be important to characterize a potential N4BP3-Nedd4 complex in neurons and analyze its impact on PTEN and Rap2 function during neurite development.
In silico analysis of the Nedd4-binding protein 3 domain structure
The domain structure of rat N4BP3 (coiled-coil and Fez1 domains) was analyzed online using the Pfam 26.0 database (Wellcome Trust Sanger Institute, Hinxton, UK).
Cloning of Nedd4-binding protein 3
We found the rat cDNA sequence of the Fezzin family member N4BP3 in public database homology searches. Using a polymerase chain reaction (PCR)-based approach, we cloned a full-length N4BP3 cDNA using a rat total brain cDNA library (Stratagene, La Jolla, CA, USA) as a template. The correct cDNA was confirmed by DNA sequencing and inserted into different bacterial and eukaryotic expression vectors, including pEGFP and pCMV-myc (both from Clontech Laboratories, Mountain View, CA, USA).
Antibodies and vector constructs
A partial cDNA of N4BP3 (encoding aa 1 to 309) was subcloned into the bacterial expression vector pGEX-4T (GE Healthcare, Freiburg, Germany). A glutathione S-transferase (GST)-N4BP3 fusion protein was expressed in Escherichia coli BL-21 and purified on Glutathione Sepharose 4B as recommended by the manufacturer (GE Healthcare). The purified fusion protein was used to generate a polyclonal N4BP3 antiserum in rabbits (Pineda Antibody Service, Berlin, Germany). This antiserum was subsequently affinity-purified using a HiTrap NHS-activated HP column loaded with GST-N4BP3 (GE Healthcare). The following primary antibodies were purchased from commercial suppliers: microtubule-associated protein 2 (MAP2; Aves Laboratories, Tigard, OR, USA), phospho-IκBα (Ser32/36) (Cell Signaling Technology, Danvers, MA, USA), GFP (Clontech Laboratories), neurofilament-associated antigen 3A10 (Developmental Studies Hybridoma Bank (DSHB), University of Iowa, Iowa City, IA, USA), Nedd4 (Novus Biologicals, Littleton, CO, USA), c-Myc (Roche Applied Science, Mannheim, Germany), β-tubulin (Sigma-Aldrich, Steinheim, Germany) and axonal growth cone antigen 2G13P (Thermo Scientific, Bonn, Germany).
The rat N4BP3- RNAi construct was generated following published methods using the pSUPER vector (Oligoengine, Seattle, WA, USA). We chose the target sequence for the N4BP3-RNAi (5′-AG ACT TGG CAG GAG GAA AA-3′) according to propositions made by Eurofins MWG Operon and the corresponding oligonucleotides were ordered from this company (Ebersberg, Germany). The RNAi-resistant Myc-N4BP3 construct was generated by site-directed mutagenesis using the QuikChange II XL Site-Directed Mutagenesis Kit (Stratagene) to introduce three different point mutations (5′-AG ACG TGG CAA GAG GAG AA-3′) within the RNAi target sequence.
For characterization of the affinity-purified N4BP3 antibody, recombinant Myc-N4BP3 protein (rat sequence) was generated using an in vitro TNT kit (Promega, Madison, WI, USA). Furthermore, HEK-293T cells (transfected with GFP-N4BP3 or Myc-N4BP3, as well as untransfected cells) or primary hippocampal cultures were lysed in Triton X-100 lysis buffer (150 mM NaCl, 50 mM Tris•HCl, 1% Triton X-100, pH 8.0, protease inhibitor mix; Roche Applied Science). Protein concentrations were determined by Bradford protein assay, and 15 μg of protein per lane were loaded for SDS-PAGE. Western blot analysis was conducted following standard protocols. Horseradish peroxidase-conjugated secondary antibodies (Dako, Glostrup, Denmark) and the SuperSignal Detection System (Thermo Scientific) were used to visualize protein bands on X-ray films (GE Healthcare).
Culturing of rat primary hippocampal neurons
The preparation of hippocampal cultures from rat was performed at embryonic stage 18 (E18), essentially as described previously. In brief, hippocampal neurons were seeded onto poly-L-lysine (0.1 mg/ml; Sigma-Aldrich) coated glass coverslips. Cells were grown in Neurobasal Medium complemented with B-27 supplement, 0.5 mM L-glutamine and penicillin/streptomycin at 100 U/ml (all reagents were purchased from Life Technologies, Darmstadt, Germany) and maintained at 37°C in a 5% CO2 atmosphere.
Cultured cells were fixed with 4% paraformaldehyde (PFA)/1.5% sucrose in phosphate-buffered saline (PBS) at room temperature for 20 min and processed for immunocytochemistry. After permeabilization of the cells with 0.1% Triton X-100 in PBS for 5 min, blocking was performed using 5% fetal calf serum in PBS followed by the primary antibody at 4°C overnight. Washing with PBS was followed by incubation with the secondary antibody coupled to Alexa Fluor 488, 568 or 647 (all from Molecular Probes) for 1 h at room temperature. The actin cytoskeleton was visualized using Alexa Fluor 647 phalloidin in some experiments. Cell nuclei were counterstained with 4′,6-diamidino-2-phenylindole, and, after further washing steps, cells were mounted in Mowiol medium. Images were captured using an upright fluorescence microscope (Axioskop 2; Zeiss, Oberkochen, Germany). For Sholl analysis, concentric circles (15, 30, 45, 60, 75, 90, 105 and 120 μm in diameter) were drawn around the soma of each neuron included in the analysis. The number of all dendrites crossing each circle was counted manually.
Vector constructs were transfected into HEK-293T or COS-7 cells using PolyFect reagent (QIAGEN, Hilden, Germany) or into hippocampal neurons using Lipofectamine 2000 reagent (Life Technologies).
Xenopus laevis embryos
X. laevis embryos were generated by in vitro fertilization, cultured in 0.1× modified Barth’s saline solution buffer (88 mM NaCl, 1 mM KCl, 2.4 mM NaHCO3, 0.82 mM MgSO4•7H2O, 0.33 mM Ca(NO3)2•4H2O, 0.41 mM CaCl•6H2O, 10 mM HEPES, pH 7.6) and staged according to a previously described protocol. Embryos were fixed either with MEMFA (0.1 M 3-(N-morpholino)propanesulfonic acid (pH 7.4), 2 mM ethylene glycol tetraacetic acid, 1 mM MgSO4 and 4% formaldehyde) for WMISH experiments or with 4% PFA in PBS for antibody staining. For later Western blot analysis, embryos were frozen at −80°C.
Whole-mount in situ hybridization and immunostaining in Xenopus laevis
To visualize the spatiotemporal expression pattern of n4bp3 during X. laevis embryogenesis, WMISH experiments were performed using a 1.447-kb digoxigenin-labeled antisense n4bp3 RNA probe detecting X. laevis n4bp3 mRNA. For cloning of the n4bp3 RNA probe, we used the following primers based on the published X. tropicalis sequence [Xenbase:XM_002936850]: n4bp3_l: 5′-ATG GGA AGT GTA AGC AGC CTA-3′; and n4bp3_r: 5′-TCT GGG CTT CAT TCT GAC GC-3′. PCR was performed using Phusion High-Fidelity DNA Polymerase (Thermo Fisher Scientific, Pittsburgh, PA, USA) and X. laevis cDNA isolated from stage 20 embryos. The PCR product was cloned into the pSC-B vector (Stratagene), and the antisense RNA probe was generated using NotI enzyme (New England Biolabs, Ipswich, MA, USA) and T3 RNA Polymerase (Roche Applied Science). WMISH experiments were performed using X. laevis embryos at different developmental stages according to standard protocols. For a more detailed analysis of n4bp3 expression, we studied vibratome sections. The monoclonal 3A10 antibody (DSHB) was further used to visualize cranial nerve fibers at E46 by immunohistochemical staining according to the method outlined by Schuff et al..
Microinjection in Xenopus laevis embryos
For loss of function experiments in X. laevis embryos, antisense MOs were obtained from Gene Tools (Philomath, OR, USA), resuspended in diethylpyrocarbonate-treated H2O and stored in aliquots at −20°C. The standard control MO sequence is 5′-CCT CTT ACC TCA GTT ACA ATT TAT A-3′, and the sequence of the n4bp3 MO is 5′-CAA TCA GGC TGC TTA CAC TTC CCA T-3′. Twenty to twenty-five nanograms of either MO were injected unilaterally in one animal dorsal blastomere of eight-cell stage embryos targeting anterior neural tissue. Correct injections were controlled by the coinjection of GFP RNA (Additional file3: Figure S3), which was generated by in vitro transcription using the mMESSAGE mMACHINE Kit (Life Technologies). To test the translational blocking efficiency of n4bp3 MO, the n4bp3 MO binding site was cloned in front of and in frame with GFP in pCS2+ vector (n4bp3 MO-GFP). One nanogram of n4bp3 MO-GFP RNA was then injected bilaterally into X. laevis embryos at two-cell stage, together with 25 ng of either the standard control or n4bp3 MO. GFP fluorescence was monitored at stage 24 of development. Furthermore, n4bp3 MO was injected bilaterally into two-cell stage X. embryos. At stage 15, embryos were fixed. Protein lysates were generated as described previously and subsequently analyzed by Western blotting.
For cell culture experiments, ten cells from three independent experiments per condition were analyzed using AxioVision version 4.8.2 software (Zeiss). For the statistical analysis of cranial nerve branching in X. laevis embryos, 20 embryos (WT, n4bp3 MO) and 23 control MO embryos from three experiments (WT, n4bp3 MO) and two experiments (control MO), respectively, were examined. All data were tested for significance by using Student’s t-test (*P < 0.05, **P < 0.01, ***P < 0.001). All animal experiments in this study were performed in accordance with the guidelines for the welfare of experimental animals issued by the federal government of Germany and by the local ethics committee at Ulm University (ID 0.103).
This study was supported by grants from the Deutsche Forschungsgemeinschaft (DFG; grants BO 1718/3-1 and 1718/4-1 to TMB and grant SFB497, TpA6 to MK). MJS is supported by Baustein 3.2, as is AMG (grant L.SBN.0081 to MJS and grant L.SBN.0083 to AMG). TMW and MS were supported by a thesis grant from the Experimental Medicine Program of the International Graduate School at Ulm University. The authors gratefully acknowledge the professional technical assistance of Maria Manz, Susanne Gerlach-Arbeiter and Petra Dietmann. They further want to thank Kristin Franke and Constantin Mett for helpful discussions.
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