Summary

Gene Delivery to Postnatal Rat Brain by Non-ventricular Plasmid Injection and Electroporation

Published: September 17, 2010
doi:

Summary

This protocol describes a non-viral method of delivery of genetic constructs to a certain area of living rodent brain. The method consists of plasmid preparation, micropipette fabrication, neonatal rat pup surgery, microinjection of the construct, and in vivo electroporation.

Abstract

Creation of transgenic animals is a standard approach in studying functions of a gene of interest in vivo. However, many knockout or transgenic animals are not viable in those cases where the modified gene is expressed or deleted in the whole organism. Moreover, a variety of compensatory mechanisms often make it difficult to interpret the results. The compensatory effects can be alleviated by either timing the gene expression or limiting the amount of transfected cells.

The method of postnatal non-ventricular microinjection and in vivo electroporation allows targeted delivery of genes, siRNA or dye molecules directly to a small region of interest in the newborn rodent brain. In contrast to conventional ventricular injection technique, this method allows transfection of non-migratory cell types. Animals transfected by means of the method described here can be used, for example, for two-photon in vivo imaging or in electrophysiological experiments on acute brain slices.

Protocol

1. Introduction Creation of transgenic animals is a powerful method of investigation of gene functions in living animals1 and for unraveling disease mechanism2,3 as well as for manipulating properties of cells4. However, the procedure is rather laborious, extremely time consuming and expensive, thus warranting the use of alternative gene delivery methods such as viral injection5, neonatal ventricular injection with electroporation6 and …

Discussion

Methods of gene delivery into living rodent brain are well established for in utero electroporation7,8,11,12 and, more recently, for postnatal electroporation6. However, these methods are based on intraventricular injection of the plasmid DNA, which may be limiting for several applications. For example, these methods do not allow targeting cells in certain brain areas such as hippocampus, nor transfection of such non-migratory cell types as cortical astrocytes. Non-ventricular injection cou…

Acknowledgements

We thank Ekaterina Karelina for help with soundtrack recording for the video, Ivan Molotkov for 3D animation and Dr. Peter Blaesse for CAG-EGFP plasmid preparation.

The work was supported by grants from the Centre of International Mobility of Finland, Finnish Cultural Foundation and the Academy of Finland.

Materials

Material Name Tipo Company Catalogue Number Comment
2A-sa dumb Tweezers, 115mm equipment XYtronic XY-2A-SA Treat with 70% ethanol for disinfection before use in surgical manipulations
Biological Temperature Controller with stainless steel heating pad equipment Supertech TMP-5b  
Borosilicate tube with filament material Sutter Instruments BF120-69-10 Glass needle
Disposable drills material Meisinger HP 310 104 001 001 008  
Dulbeco’s PBS 10X reagent Sigma D1408  
Dumont #5 forceps, 110 mm equipment FST 91150-20 Treat with 70% ethanol for disinfection before use in surgical manipulations
Ealing microelectrode puller equipment Ealing 50-2013 Vertical electrode glass puller
Ethilon monofil polyamide 6-0 FS-3 16 mm 3/8c material Johnson & Johnson Medical EH7177H Surgical threads
Exmire micro syringe 10.0 ml equipment Exmire MS*GLLX00 Gas-tight syringe
Fast Green reagent Sigma F7252  
Forceps electrodes equipment BEX LF650P3 Treat with 70% ethanol for disinfection prior to use
Foredom drill control equipment Foredom FM3545 Surgical drill power supply and control. Currently available analogue is micromotor kit K.1070 (Foredom)
Foredom micro motor handpiece equipment Foredom MH-145 Currently available analogue is micromotor kit K.1070 (Foredom)
Gas anesthesia platform for mice equipment Stoelting 50264 Assembled on stereotaxic instrument
Isoflurane reagent Baxter FDG9623  
Micro dressing forceps, 105 mm equipment Aesculap BD302R Treat with 70% ethanol for disinfection before use in surgical manipulations
Microfil material WPI MF34G-5 Micro syringe filling capillaries
Mineral oil reagent Sigma M8410  
NanoFil Syringe 10 microliter equipment WPI NANOFIL Hamilton syringe
plasmid CAG-EGFP reagent     Extracted and purified with EndoFree Plasmid Maxi Kit (Qiagen) and dissolved in nuclease free water to concentration 1.5 mg/ml
Pulse generator CUY21Vivo-SQ equipment BEX CUY21Vivo-SQ  
Schiller electrode gel reagent Schiller AG 2.158000 Conductive gel
Small animal stereotaxic instrument equipment David Kopf Instruments 900  
Stoelting mouse and neonatal rat adaptor equipment Stoelting 51625 Assembled on stereotaxic instrument. Treat earbars with 70% ethanol for disinfection before use in surgical manipulations
Student iris scissors, straight 11.5 cm equipment FST 91460-11 Treat with 70% ethanol for disinfection before use in surgical manipulations
Sugi absorbent swabs 17 x 8 mm material Kettenbach 31602 Surgical tampons
UMP3 microsyringe pump and Micro 4 microsyringe pump controller equipment WPI UMP3-1 Microinjector and controller
Univentor 400 Anesthesia Unit equipment Univentor 8323001  

Riferimenti

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Citazione di questo articolo
Molotkov, D. A., Yukin, A. Y., Afzalov, R. A., Khiroug, L. S. Gene Delivery to Postnatal Rat Brain by Non-ventricular Plasmid Injection and Electroporation. J. Vis. Exp. (43), e2244, doi:10.3791/2244 (2010).

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