Gene delivery in mouse auditory brainstem and hindbrain using in utero electroporation
© David et al. 2014
Received: 5 June 2014
Accepted: 14 July 2014
Published: 26 July 2014
Manipulation of gene expression via recombinant viral vectors and creation of transgenic knock-out/in animals has revolutionized our understanding of genes that play critical roles during neuronal development and pathophysiology of neurological disorders. Recently, target-specific genetic manipulations are made possible to perform in combination with specific Cre-lines, albeit costly, labor-intensive and time consuming. Thus, alternative methods of gene manipulations to address important biological questions are highly desirable. In this study, we utilized in utero electroporation technique which involves efficient delivery of hindbrain-specific enhancer/promoter construct, Krox20 into the third ventricle of live mouse embryo to investigate green fluorescent protein (GFP) expression pattern in mouse auditory brainstem and other hindbrain neurons.
We created a GFP/DNA construct containing a Krox20 B enhancer and β-globin promoter to drive GFP expression in the hindbrain via injection into the third ventricle of E12 to E13.5 mice. Electrical currents were applied directly to the embryonic hindbrain to allow DNA uptake into the cell. Confocal images were then acquired from fixed brain slices to analyze GFP expression in mouse whole brain at different postnatal stages (P6-P21). By using a cell-type specific enhancer as well as region specific injection and electroporation, robust GFP expression in the cerebellum and auditory brainstem but not in the forebrain was observed. GFP expression in calyx of Held terminals was more robust in <P15 compared to >P15 mice. In contrast, GFP expression in MNTB neurons was more prevalent in >P15 compared to <P15. In regards to the relative expression of GFP versus the synaptic marker Vglut1, percentage fluorescence GFP intensity in the calyx was higher in P11 to P15 than P6 to P10 and P16 to P21 groups.
Taken together, this technique would potentially allow hindbrain-specific genetic manipulations such as knock-down, knock-in and rescue experiments to unravel critical molecular substrates underpinning functional and morphological remodeling of synapses as well as understanding the pathophysiology of certain neurological disorders targeting not only the auditory brainstem but also other parts of hindbrain, most notably the cerebellum.
KeywordsIn utero electroporation Gene delivery Krox20 Hindbrain Calyx of Held MNTB GFP
Recent advances in understanding genetic mechanisms underlying normal neuronal development and pathophysiology of a number of nervous disorders have been made possible by gene manipulations using loss- and gain-of-function transgenic animal models via viral infection or Cre-Lox system. However, it is not always feasible to restrict or repress expression of genes spatially and temporally, and the generation of transgenic animals and recombinant viruses are costly, time-consuming and labor-intensive [–]. To address these issues, alternative and innovative method of gene delivery into the mouse developing embryo known as in utero electroporation has been developed. To date, in utero electroporation has been successfully used to study structures in cortex, retina, thalamus and hypothalamus [–] as well as in dendritogenesis and migration of developing cerebellar Purkinje cells []. However, there is no report yet on gene delivery on murine hindbrain, and specifically the auditory brainstem using the in utero electroporation technique.
The development of vertebrate hindbrain is determined by the formation of segmentation processes along the anteroposterior axis leading to the establishment of transversal morphological units called rhombomeres (r). The rhombomeres are structural units that direct cell lineage patterns and area of gene expression [–]. The molecular control of cell- and tissue-type specification within developing hindbrain provides insights into the genetic bases of the most common human developmental brainstem and cerebellar disorders such as congenital deafness, migraine, vestibulopathies, Joubert syndrome, Dandy-Walker malformation, spinal cerebellar ataxias (SCA) and many other hindbrain disorders. Indeed, several causative genes have been identified for cerebellar and brainstem disorders [–]. Thus, it is imperative to develop a method to efficiently deliver gene(s) into the hindbrain using both region-specific injection and incorporating a hindbrain-specific enhancer construct.
Krox20, a C2H2-type zinc finger transcription factor and immediate early gene, is highly specifically active in r3 and r5 of the developing hindbrain giving rise to majority of the brainstem and cerebellar neurons []. Krox20 mRNA is first detected in prospective r3 and r5 at approximately embryonic (E) 8 and 8.5, respectively. At E9.5, Krox20 mRNA expression begins to disappear in r3 and at E10.5 expression starts to disappear in r5. However, between E14.5 and E16.5, a second period of transcription was observed in two dorsolateral columns of brainstem [–]. In regards to cellular localization and developmental regulation of Krox20 protein expression, De et al. showed that Krox20 has prominent role towards the maturation of motoneurons and somatosensory hindbrain neurons, Purkinje cells and components of auditory brainstem []. Given the role of Krox20 in hindbrain development, we utilized the cis-regulatory element Krox20 B enhancer [] to investigate the possibility of hindbrain-specific gene delivery. We cloned fluorescent labeled DNA construct that would drive expression into the mouse hindbrain. We incorporated Krox20 B enhancer upstream of β-globin promoter and enhance green fluorescent protein (EGFP) reporter to test the efficiency and specificity of delivering genes via in utero electroporation. Confocal images from fixed postnatal mouse brain slices were obtained and analyzed to evaluate competence of this gene delivery technique. Our results demonstrated that Krox20 can drive the expression of GFP in subsets of neurons in hindbrain, and hence provide a proof of principle that genes of interest can be targeted via in utero electroporation for molecular perturbations to facilitate understanding molecular underpinnings of cerebellum and brainstem during normal development and diseases.
GFP expression patterns in hindbrain neurons
Developmental dependence of GFP expression in pre- and postsynaptic elements of synapses
The calyx of Held-principle neuron synapse in the medial nucleus of trapezoid body (MNTB) in the superior olivary complex (SOC) in auditory brainstem is an important relay station in the sound localization circuit, capable of high fidelity neurotransmission to project well-timed and sustained inhibition to other auditory nuclei. Because of its giant size and accessibility to patch-clamp recordings, this large axosomatic terminal at this synapse has emerged as one of the most prominent preparations for anatomists and physiologists to study important questions with respect to fundamental principles of developmental plasticity in presynaptic morphology, excitability and transmitter release [,]. Aside from acute stereotactic surgery to inject viral constructs into postnatal mice synapse [,], it has been difficult to perform molecular perturbations in order to study mechanisms underlying structural and functional remodeling in the developing calyx of Held-MNTB. Therefore, it is imperative to develop innovative methods that would allow genetic and molecular manipulations to target these synapses early in development. In this study, we explored the potential utility of in utero electroporation technique via analysis on the developmental progression of GFP expression from postnatal (P) pups electroporated with CB-Krox20-GFP DNA construct.
The primary goal of this study is to establish a technique that would allow manipulations of genes in the auditory brainstem and other hindbrain neurons, and potentially use this method to understand molecular underpinnings of morphological and functional plasticity of model synapses during normal development and diseases. Previously, in utero electroporation-mediated gene delivery method has been utilized to study structures in cortex, retina, thalamus and hypothalamus [–]. However, to our best knowledge, an efficient gene delivery method targeting the hindbrain particularly the auditory brainstem has not been explored. In this work, we established in utero injection and electroporation technique targeting subsets of the hindbrain neurons by incorporating both Krox20 construct and region-specific injection.
We have shown that by delivering Krox20 B enhancer and EGFP reporter construct into the third ventricle of embryonic E12 to E13.5 mouse, robust expression of GFP in brainstem and cerebellum (e.g. Purkinje and granule cells) was observed. We explored the potential utility of this technique in synaptic physiology with particular emphasis on the calyx of Held-MNTB synapse. We demonstrated that the distribution and level of GFP expression in the MNTB principal neurons and the calyx of Held vary during development (Figure 4, Figure 5 and Figure 6). On all three stages of development used in this study, fraction of cells expressing GFP on both MNTB and calyx showed no significant difference. However, in pre-hearing and intermediate animals, GFP expression is predominantly in the calyx. Conversely, post-hearing mice showed more expression in MNTB neurons. From these results, we can infer the usefulness of in utero electroporation technique in manipulating genes in the presynaptic terminal, and/or the postsynaptic neuron under visual cues of GFP fluorescence in either element or both. For example, rescue experiments such as overexpression of wildtype genes encoding for specific synaptic proteins in genetically knockout or mutant mouse lines can be used to assess their respective role(s) in presynaptic vesicle fusion and exocytosis by using P6 to P15 animals. On the other hand, older mice i.e. P16 to P21 can be used in experiments requiring investigation on the role of a particular protein in postsynaptic neurons. Conversely, one can also utilized this technique to perform gene knockdown or knockout by electroporating siRNA or dominant negative constructs. Alternatively, this technique can also be applied to investigate gene function in spatial and/or temporal manner by incorporating tamoxifen-inducible Cre recombinases in Krox20 B enhancer construct that can be transiently expressed. Previous studies have used such a strategy to specifically knockout presynaptic proteins (i.e. RIM) with the Krox20 driver mouse to target the calyx of Held-MNTB synapse [], but our result showing significant GFP expression in the postsynaptic element after P15 raises the caution of its specificity and developmental dependence. We suggest that in utero electroporation method presents an alternative opportunity for variety of genetic manipulations other than stereotactic surgeries in postnatal mice, in which mechanic damage to brain tissues is inevitable. It is however important to note that embryonic survival rate is low when first learning the technique but with practice it rises to 50%. It is also important to consider performing the procedure with minimal stress to both mother and litter to avoid pre-term abortion.
Overall, we established a relatively efficient and regional and enhancer-specific gene delivery in hindbrain with emphasis on auditory brainstem via in utero electroporation technique. This method would potentially allow target-specific knock-down, knock-in as well as rescue experiments to unravel critical molecular substrates underpinning functional and morphological remodeling of synapses during early development and diseases.
All animal procedures were performed in accordance with The Hospital for Sick Children Animal Care Committee and Canadian Council on Animal Care guidelines for animal research. Pregnant mice (E12.5-E13.5) were purchased from Charles River Laboratories, Wilmington, MA, USA.
For construction of Krox20 B enhancer/β-globin promoter DNA clone encoding GFP in hindbrain structures, the CMV promoter region of pEFGP-C1 vector (Clontech, Invitrogen) was excised and replaced with Krox20 B enhancer and β-globin promoter from cB-LacZ construct kindly donated by Dr. Pascale G-Heberstreit (INSERM, France). Briefly, the ~650 base pairs Krox20 B enhancer/β-globin promoter region of cB-LacZ construct was amplified with Elongase enzyme (Invitrogen) using the oligonucleotides CB1GKrox-AseI: 5′ CGT CAT ATT AAT CCT GCA GGC GGC CGC 3′ and CB1GKrox20-NheI: 5′ C ATA TAT GCT AGC GGC GCC GCG CTC TGC 3′. Polymerase chain reaction (PCR) products were then run in 0.8% agarose gel, excised, purified and subcloned in pGEMT-easy vector and subsequently grown on agar plates for blue/white screening. Selected white colonies were grown into LB media and plasmid DNA from each culture was digested with AseI and NheI and run in 0.8% agarose gel to confirm positive cloning. The Krox20 B enhancer/β-globin promoter AseI/NheI fragment was excised, purified and moved to pEFGP-C1 vector to create the CB-Krox20-GFP construct (Figure 1). This clone was subsequently used for injection into the mouse embryo. All plasmid sequences were confirmed via DNA sequencing.
In utero electroporation
Efficient gene delivery to murine hindbrain was performed using pregnant CD1 mice (Figure 2). Pregnant CD1 mouse (E12-E13.5) was anaesthetized by halothane and a small abdominal midline incision was made. Uterine horns were carefully pulled out onto 37°C pre-warmed saline-moistened cotton gauze, which is placed around the wound. Starting with one horn of the uterus, CB-Krox20-GFP DNA construct or pCDNA3.1 (−) (~1 to 2 μg) mixed with 0.05% trypan blue (Sigma, St. Louis. MO) was injected by air pressure into the lateral ventricles using a mouth-controlled micropipette (Drummond Scientific, Broomall, PA, USA). The tip of the micropipette was directed towards the third ventricle to target hindbrain structures particularly the brainstem. The embryonic brain vesicles are open at early embryonic stages such that DNA injected into the lateral ventricles will flow into the third ventricle. After DNA injection, platinum tweezer-type electrodes (5 mm diameter, Protech, Boerne, Texas, USA) briefly soaked in saline were softly placed on the target region, and five 40 V square of 50 millisecond duration with 950 millisecond intervals were applied by using CUY21EDIT (NepaGene, Chiba, Japan). After electroporation, the uterine horns were carefully replaced back into the abdomen and the wound was closed using sterile surgical 4.0 CV-22 taper sutures (Covidien, Mansfield, MA, USA). Shorter surgical time is preferred as it will yield better viability (<30 minutes per mother). Anafen (10 mg/mL) was injected subcutaneously for post-operative pain and the surgical mother was allowed to recover in a heating pad.
Brain slices preparation
Brainstem slices were prepared from P6 to P21 mice electroporated with CB-Krox20-GFP DNA construct. Mice were decapitated with small guillotine and brains were immediately immersed into semi-frozen modified artificial cerebral spinal fluid (ACSF) containing the following (in mM): 125 NaCl, 2.5 KCl, 10 glucose, 1.25 NaH2PO4, 2 Na-pyruvate, 3 myo-inositol, 0.5 ascorbic acid, 26 NaHCO3, 3 MgCl2 and 0.1 CaCl2 at a pH of 7.3 when oxygenated (95% O2 and 5% CO2). Transverse slices of the auditory brainstem containing the medial nucleus of the trapezoid body (MNTB) were cut at a thickness of 100–200 μm using a microtome (VT1000S:Leica, Nussloch, Germany) followed by incubation at 37°C in ACSF containing the following (in mM): 125 NaCl, 2.5 KCl, 10 glucose, 1.25 NaH2PO4, 2 Na-pyruvate, 3 myo-inositol, 0.5 ascorbic acid, 26 NaHCO3, 1 MgCl2 and 2 CaCl2 at pH of 7.3 when oxygenated (95% O2 and 5% CO2) for 1 hour before experimentation.
Whole brain sagittal and transverse slices were also prepared to determine whether GFP was exclusively expressed within the hindbrain (brainstem and cerebellum) or expression extends towards the forebrain (e.g. cortex and hippocampus). Electroporated mice were anaesthesized using sodium pentobarbital 40 μg per gram body weight administered intraperitoneally. Brains were washed with 1X phosphate buffered saline (PBS) via intra-cardiac perfusion and subsequently fixed by perfusing with 4% paraformaldehyde. Transverse and sagittal brain slices were cut at a thickness of 50 μm using microtome (VT1000S: Leica, Nussloch, Germany).
Immunohistochemistry and image acquisition
Brainstem slices were fixed in 4% paraformaldehyde in PBS for 30 minutes then rinsed three times with PBS. Slices were then permeabilized in 0.2% Triton X-100 and rinsed three times. The synaptic marker, vesicular glutamate transporter-1 (Vglut1) (Millipore, Temecula, CA, USA) was used to label presynaptic terminals. Following permeabilization, slices were incubated in guinea pig anti-Vglut1 (1:750) overnight at room temperature with gentle agitation. Slices were then washed with PBS prior to incubation in secondary antibody conjugated to Cy3 (1:500; Goat anti-Guinea Pig, Jackson Laboratories, West Grove, PA, USA). After several rinses with PBS, slices were mounted using Vectashield (Vector Laboratories, Burlingame, CA, USA). Fixed transverse and sagittal brain sections were mounted using Vectashield mixed with 4′, 6-diamidino-2-phenylindole (DAPI) to stain for nuclei.
Confocal images and z stack images were acquired with a Zeiss LSM 510 Multiphoton Laser Scanning Microscope equipped with, 405, 488 and 514 nm argon laser lines to visualize nuclei (DAPI), GFP, and Cy3, respectively. Confocal scans were acquired using a 63X (N.A. 1.4) oil objective and the appropriate dichroic filters (MBS 488 and MBS 514). 3D images were rendered using Volocity software (Perkin Elmer, USA).
Three age groups were analyzed: P6 to P10 (pre-hearing); P11 to P15 (intermediate); and P16 to P21 (post-hearing). Relative fraction of cells expressing GFP from MNTB or calyx alone or from both MNTB and calyx were calculated from at least 14 images per age group. Relative expression of GFP driven by Krox20 B enhancer in the presynaptic terminal was obtained by determining the ratio of the fluorescence intensity of GFP and Vglut1 from a minimum of 100 cells from each age group as mentioned above. All graphs and statistical analyses were performed using ORIGIN 7.5 (Northampton, MA). Data represents mean±s.e.m. and statistical difference were estimated at p < 0.05 (ANOVA) from a minimum of three animals per age group.
Green fluorescent protein
Lateral superior olive
Medial nuclei of the trapezoid body
Phosphate buffered saline
Spinal cerebellar ataxias
Vesicular glutamate transporter 1
Ventral cochlear nuclei
This work was funded by a grant from Canadian Institute of Health Research (CIHR) to Dr. Lu-Yang Wang, and a postdoctoral fellowship award from the Research Training Centre of the Hospital for Sick Children (RestraComp Postdoctoral Fellowship) to Dr. Laurence S. David. The authors would like to thank Dr. Giovanbattista Grande for assistance in confocal microscopy, Dr. Pascale G-Heberstreit, INSERM, France for the gift of Cb-Krox20-LacZ construct and Dr. Freda Miller for generously allowing us to use the CUY21EDIT electroporator utilized in this study.
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