PUBLICATION

An automated system for intracellular and intranuclear injection

Authors
Hogg, R.C., Bandelier, F., Benoit, A., Dosch, R., and Bertrand, D.
ID
ZDB-PUB-080226-16
Date
2008
Source
Journal of Neuroscience Methods   169(1): 65-75 (Journal)
Registered Authors
Dosch, Roland
Keywords
Xenopus oocyte, Zebrafish, Intranuclear injection, RNA injection, Electrophysiology, Lab automation, Drug screening
MeSH Terms
  • Animals
  • Automation/instrumentation
  • Automation/methods*
  • Biological Assay/methods*
  • Cell Culture Techniques/methods
  • Cell Nucleus/drug effects
  • Cell Nucleus/genetics
  • Cell Nucleus/ultrastructure
  • Cytological Techniques/instrumentation
  • Cytological Techniques/methods*
  • DNA, Complementary/genetics
  • DNA, Complementary/pharmacology*
  • Drug Evaluation, Preclinical/methods
  • Female
  • Ion Channels/drug effects
  • Ion Channels/genetics
  • Microinjections/instrumentation
  • Microinjections/methods*
  • Oocytes/cytology
  • Oocytes/drug effects*
  • Oocytes/metabolism
  • RNA, Messenger/genetics
  • RNA, Messenger/pharmacology*
  • Xenopus laevis
  • Zebrafish
PubMed
18243328 Full text @ J. Neurosci. Methods
Abstract
The Xenopus oocyte expression system has played an important role in the study of cellular proteins, particularly in the field of membrane physiology; expression of transporters and ion channels has significantly advanced our knowledge of these membrane proteins and the rapid and easy expression of mutants has been crucial in many structure-function studies. Xenopus oocytes are an expression system in many ligand-binding assays and in functional screening for ion channel modulators. Several commercially available automated technologies use this system, generating a demand for large numbers of oocytes injected with ion channel genes. Injection of oocytes with genetic material is generally carried out manually. Here we describe an automated system capable of injecting up to 600 oocytes per hour. Oocytes are contained in microplates with conical wells, a simple calibration procedure by the operator is required and pipette filling and oocyte injection are carried out automatically. Following intracellular injection of mRNA coding for ligand-gated ion channels close to 100% of oocytes tested positive for expression, and intranuclear injection of cDNA gave a rate of expression >50%. Moreover, we demonstrate that this method can also be successfully applied to inject zebrafish embryos and could be extended to other cell types.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping