mRNA binding protein staufen 1-dependent regulation of pyramidal cell spine morphology via NMDA receptor-mediated synaptic plasticity
© Lebeau et al; licensee BioMed Central Ltd. 2011
Received: 18 April 2011
Accepted: 2 June 2011
Published: 2 June 2011
Staufens (Stau) are RNA-binding proteins involved in mRNA transport, localization, decay and translational control. The Staufen 1 (Stau1) isoform was recently identified as necessary for the protein synthesis-dependent late phase long-term potentiation (late-LTP) and for the maintenance of mature dendritic spines and synaptic activity in hippocampal CA1 pyramidal cells, strongly suggesting a role of mRNA regulation by Stau1 in these processes. However, the causal relationship between these impairments in synaptic function (spine shape and basal synaptic activity) and plasticity (late-LTP) remains unclear. Here, we determine that the effects of Stau1 knockdown on spine shape and size are mimicked by blocking NMDA receptors (or elevating extracellular Mg2+) and that Stau1 knockdown in the presence of NMDA receptor blockade (or high Mg2+) has no further effect on spine shape and size. Moreover, the effect of Stau1 knockdown on late-LTP cannot be explained by these effects, since when tested in normal medium, slice cultures that had been treated with high Mg2+ (to impair NMDA receptor function) in combination with a control siRNA still exhibited late-LTP, while siRNA to Stau1 was still effective in blocking late-LTP. Our results indicate that Stau1 involvement in spine morphogenesis is dependent on ongoing NMDA receptor-mediated plasticity, but its effects on late-LTP are independent of these changes. These findings clarify the role of Stau1-dependent mRNA regulation in physiological and morphological changes underlying long-term synaptic plasticity in pyramidal cells.
KeywordsSchaffer collateral synapses RNA transport late LTP spontaneous activity-driven potentiation spine morphogenesis
Localization of mRNAs to synaptic sites and their subsequent translation have emerged as important mechanisms contributing to synapse-specific plasticity [1, 2]. Thus, mRNA binding proteins (RBPs), which are key players in the transport of mRNAs, may be selectively implicated in various forms of plasticity that depend on the transport and local translation of specific transcripts. Staufen (Stau) [3, 4], fragile × mental retardation protein (FMRP) [5, 6], zipcode-binding proteins  and cytoplasmic polyadenyation element binding protein (CPEB) [8, 9] are RBPs known to be implicated in mRNA dendritic localization and translation in neurons.
Notably, Stau is implicated in regulation of mRNAs required for memory formation in Drosophila and Aplysia [10, 11]. In mammals, the two members of the Stau family, Stau1 and Stau2, are present in distinct ribonucleoprotein (RNP) complexes  and associate with different mRNAs . Stau1 is required for the transport of mRNAs necessary for long-term potentiation at hippocampal synapses, as knockdown of Stau1 impaired dendritic transport of CaMKIIα mRNA in hippocampal neurons . Moreover, downregulation of Stau1 also prevented the translation-dependent late phase LTP (late-LTP) induced by forskolin in CA1 pyramidal cells. However, the translation-independent early phase LTP was intact, suggesting an essential role of Stau1-dependent mRNA regulation in protein synthesis associated with late-LTP . Interestingly, we recently found that Stau2-dependent regulation of mRNA was essential specifically for translation-dependent mGluR long-term depression, uncovering selective mechanisms of mRNA regulation for different forms of translation-dependent long-term synaptic plasticity .
Long-term changes in synaptic function are associated with changes in dendritic spines [16, 17]. Indeed, we found that, in association with the impairment in late-LTP, Stau1 knockdown resulted in a shift from regular short spines to longer thin spines, suggesting a role in the formation and/or maintenance of mature spine shape . However, since a form of NMDA-mediated plasticity, referred to as spontaneous activity-driven potentiation (SAP) , may be ongoing in our slice culture conditions and induce changes in spine shape [19–21], it is unknown whether the effects of Stau1 knockdown on late-LTP were due to its actions on spine morphogenesis, or vice versa. Thus, our aims were to test directly if preventing SAP by blocking NMDAR function (or elevating extracellular Mg2+) would influence the changes in dendritic spine morphology induced by Stau1 knockdown, and whether the changes induced by blocking SAP were in turn required for the effect on Stau1 knockdown on late-LTP. We found that while Stau1 is involved in spine morphogenesis through NMDAR-mediated SAP, the change in spine morphogenesis was not important for the effect of Stau1 on late-LTP.
Organotypic hippocampal slice cultures
All experiments were done in accordance with animal care guidelines at Université de Montréal, with the approval of the ethics committee at Université de Montréal (CDEA #10-003), and followed internationally recognized guidelines. Organotypic hippocampal slices were prepared and maintained in culture as previously described [14, 22].
siRNAs and transfections
siRNA target sequences for rat were as described . Biolistic transfection of neurons in organotypic slice cultures was performed using a Helios gene gun (Bio-Rad, CA) following manufacturer's instructions as previously [14, 22]. Electrophysiological recordings and cell imaging experiments were performed 48 hours after transfection and the experimenter was blind to transfection treatments.
Individual slice cultures were transferred to a submerged-type recording chamber continuously perfused (at 1-2 ml/min) with artificial cerebrospinal fluid (ACSF) composed of (in mM): 124 NaCl, 2.5 KCl, 1.25 NaH2PO4, 1.3 MgSO4, 26 NaHCO3, 10 dextrose, 2.5 CaCl2, 2 μM adenosine, saturated with 95% O2 and 5% CO2, pH 7.4, as previously . Field excitatory postsynaptic potentials (fEPSPs) were evoked by Schaffer collateral stimulation (30s-1) and recorded from CA1 stratum radiatum with a glass microelectrode (2-3 MΩ) filled with 2M NaCl, as previously .
Imaging and morphological analysis
Slices were fixed with 4% paraformaldehyde and EYFP-transfected CA1 pyramidal neurons were randomly selected based on green fluorescence and characteristic morphology. Z-stacks were collected from the secondary branches of apical dendrites using a confocal laser scanning microscope LSM 510 (Carl Zeiss, Kirkland QC) and spines were analyzed using LSM 510 software as previously . Briefly, spines were categorized in three different classes on the basis of length and shape : 1 - filopodia, long protrusions (> 1 μm) without a spine head; 2 - elongated spines, long protrusions (> 1 μm) with a small head at the tip; and 3 - regular spines, short protrusions (< 1 μm) including stubby and mushroom-type spines.
Spine changes induced by NMDA receptor blockade, high Mg2+ and Stau1 siRNA treatment.
High Mg2+ (12 mM)
High Mg2+ (12 mM)
Spine density (spine/μm)
0.29 ± 0.02
0.21 ± 0.02*
0.34 ± 0.03
0.28 ± 0.02
0.19 ± 0.02
0.34 ± 0.03
Spine length (μm)
1.15 ± 0.02
1.3 ± 0.02*
1.3 ± 0.02*
1.29 ± 0.02§
1.35 ± 0.03
1.32 ± 0.03
(% of total)
49.75 ± 3.1
32.3 ± 2.7*
37.9 ± 2.2*
31.77 ± 2.2§
30.19 ± 3
36.8 ± 2.6
40.92 ± 2.3
54.68 ± 2.3*
50.3 ± 2.3*
51.49 ± 2§
51.35 ± 2.7
53.1 ± 2.7
9.33 ± 1.5
13.02 ± 1.9
11.8 ± 1.6
16.74 ± 1.4
15.57 ± 3
10.2 ± 1.5
Although spine density was not affected by Stau1 down-regulation, spine length and shape were modified (Table 1). Interestingly, blocking SAP had the same effect on spine length and shape as Stau1 knockdown. Indeed, spine length was increased in medium containing high Mg2+ or AP5 (compared to normal medium) in siRNA-CTL transfected cells (Table 1 and Figure 1C), consistent with the idea that impairing NMDAR-mediated SAP prevents the formation of mature short spines. A similar increase in spine length was also observed in siRNA-STAU1 transfected cells (compared to siRNA-CTL) in normal medium as previously reported . However, siRNA-STAU1 transfection in slices incubated in high Mg2+ or AP5 had no further effect on spine length (compared to siRNA-CTL CTL in high Mg2+ or AP5, respectively) (Table 1 and Figure 1C), suggesting that NMDAR-mediated SAP blockade occludes Stau1 knockdown consequences on spine length. Likewise in the case of spine shape, changes in the proportion of regular and elongated spines were similar in siRNA-CTL transfected cells treated with high Mg2+ or AP5 (compared to normal medium) and in siRNA-STAU1 transfected cells in normal medium (compared to siRNA-CTL in normal medium): a decrease in regular spines and an increase in elongated spines (Table 1 and Figure 1D). Once again, there was no further effect of high Mg2+ or AP5 medium in siRNA-STAU1 transfected cells (relative to siRNA-CTL in high Mg2+ or AP5, respectively). These results indicate that NMDAR-mediated SAP blockade occludes Stau1 knockdown consequences on spine shape. Overall, these results suggest that SAP, mediated by NMDA receptors, leads to changes in spine size and shape over time in slice cultures and that these effects require Stau1. Thus, blocking either NMDA receptor mediated activity or Stau1 expression has the same effect on spine size and shape, and there are no additive effects when the two treatments are combined.
Our principal findings suggest that the mRNA binding protein Stau1 is implicated in the transport or regulation of mRNAs that are involved in long-term alterations of pyramidal cell dendritic spine morphology through NMDA receptor-mediated synaptic plasticity. NMDA receptors are crucial for synaptic plasticity and learning and memory . During LTP induction, Ca2+ entry through NMDAR activates multiple signalling pathways . The maintenance of the enduring changes in synaptic efficacy consists in two phases. An early phase (early-LTP) is protein synthesis-independent and is characterized by phosphorylation of pre-existing proteins present at the synapse and synaptic insertion of AMPA receptors . A longer-lasting late phase of LTP (late-LTP) is transcription- and translation-dependent  and is presumably associated with structural alterations of synapses that are reflected in part by changes in dendritic spine morphology . Indeed, normal NMDA receptor function is thought to support morphological and structural stability of spines  and blockade of NMDA receptor activity favours the formation of immature type of spines . In addition, spontaneous activity in hippocampal slice cultures induces NMDAR-mediated potentiation of synaptic transmission, referred to as spontaneous activity-driven potentiation (SAP; ). During SAP, NMDAR-activity leads to synaptic insertion of GluR1  and a stable increase in spine size , analogous to changes occurring during LTP . Our findings are consistent with a model in which NMDAR-dependent signalling activates Stau1-dependent mechanisms of mRNA regulation during LTP and SAP induction, which lead to translation of mRNAs necessary for a long-lasting increase in synaptic efficacy, ultimately reflected as stable increases in mature spine shape. Stau1 effects on spine morphology and late LTP may also reflect different cell biological processes (both requiring NMDA receptors and/or transmitter release from presynaptic neurons), with spine morphology changes reflecting a slow function over a much longer time scale (dependent on SAP and RNA transport), and late LTP implicating a more rapid regulation of RNA transport. In addition, we cannot rule out the possibility that more subtle effects of Stau1 on spine morphology, undetected in the present study, may be related to its blocking effect on late LTP.
Our findings that knockdown of Stau1 impairs late-LTP, without affecting the early form of LTP or basal transmission , is consistent with Stau1 regulation of the translation/transport of mRNAs, but the specific role that Stau1 plays is still not clear. In the context of late-LTP, the mRNAs that are translated can consist of previously transcribed plasticity-related mRNAs that were transported constitutively to synapses prior to LTP induction  or newly transcribed mRNAs that need to be transported to the activated synapse for local translation . Activity-dependent localization of specific mRNAs in dendrites has been demonstrated in cultured neurons [31–33] and in vivo [34, 35], providing compelling support for the idea that glutamate receptor signalling may regulate dendritic mRNA transport and docking at postsynaptic sites in long-term plasticity. Stau1 was shown to be involved in the constitutive transport in dendrites of plasticity-related mRNAs such as CaMKIIα mRNA  supporting a role for Stau1 in constitutive transport of plasticity-related mRNAs. Mutant mice with impaired dendritic translation of CaMKIIα mRNA show impairments in late-LTP and hippocampal-dependent memory . Thus, CaMKIIα mRNA is a likely mRNA regulated by Stau1 during both LTP  and SAP . It remains to be determined if other mRNAs known to be regulated in late-LTP, like Arc and PKMζ [37–39], are similarly regulated in Stau1-dependent fashion. Thus, LTP and SAP could be blocked due to the lack of these mRNAs in dendrites when plasticity is induced. It is also possible that Stau1 is critical for the translation/transport of mRNAs induced by LTP. Indeed, neuronal activity induced by depolarization was shown to significantly increase RNP containing Stau2 in dendrites of cultured neurons , indicating a role of Stau2 in activity-dependent transport of mRNA. Further studies will be required to define the precise manner by which Stau1 regulates SAP and LTP.
In a recent study with a mutant mouse expressing a truncated Stau1 protein lacking the functional RNA-binding domain 3 (RBD3), cultured hippocampal neurons displayed deficits in dendritic delivery of Stau1-containing RNP, as well as reduced dendritic tree and fewer synapses, indicating that Stau1 is crucial for synapse development in vitro . These mice showed impaired locomotor activity but no significant deficit in hippocampal-dependent learning and memory, although the lack of a deficit in hippocampal function may reflect compensatory changes involving other proteins or genetic background effects . It would be interesting to determine if impairments in late-LTP are present in these mice to examine if Stau1-dependent mRNA regulation in long-term plasticity is dependent on the functional RBD3 domain.
In conclusion, we found that Stau1 involvement in spine morphogenesis is dependent on NMDA receptor-mediated plasticity in hippocampal pyramidal cells. We also found that Stau1 is required for late-LTP, independently of its role in spine morphogenesis. These findings clarify the role of Stau1-dependent mRNA regulation in the physiological and morphological changes at pyramidal cell synapses during long-term plasticity underlying hippocampal-dependent learning and memory.
This research was supported by the Canadian Institutes of Health Research (CIHR Team in Memory Grant, grant #CTP-79858, JCL; CIHR grant MOP 15121, WS), Fonds de la recherche en santé du Québec (Groupe de recherche sur le système nerveux central; grant #5249; JCL, WS, LD) and the Canada Research Chair Program (Canada Research Chair in Cellular and Molecular Neurophysiology; grant #950-213424; JCL). GL was supported by a Savoy Foundation studentship. The authors would like to thank Julie Pepin and Catherine Bourgeois for excellent technical assistance.
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