Real-time fluorescent quantitative RT-PCR assay for the expression of metallothioneins in rat hippocampal neurons

Metallothioneins (MTs) are short, cysteine-rich proteins for heavy metal homeostasis and detoxification; they can bind a variety of heavy metals and also act as radical scavengers. In brain cells, they play a neuroprotective role in many aspects. However, because the previous methods can't quantify their gene expression at the mRNA level, their regulation in brain, especially in neurons, is not well known by now. In this study, we use a more accurate method, the real-time fluorescent quantitative RT-PCR technique, to determine the expression of three MT isomers on 100 μM zinc exposure after 0, 2, 4, 6 and 8 hours in primary culture rat hippocampal neurons. The result shows that the expression of all three MT isomers was higher compared with the values determined by other methods. This means that the roles played by neuron MTs in protecting neurons injury on zinc fluctuation was even stronger than what has been suspected before. In conclusion, our study proved that the real-time fluorescent quantitative RT-PCR technique is a simple, rapid and more precise method than previous techniques in the detection of gene expression, especially for those genes with low abundant mRNA. Our study also suggest that may of the past studies about gene expression should be verified by real-time Fluorescent quantitative RT-PCR once more in order to reach a more scientific explanation on certain problem.

[1]  A sensitive time-resolved fluorescent immunoassay for metallothionein protein. , 2003, Journal of immunological methods.

[2]  J. Nacher,et al.  Cytochemical techniques for zinc and heavy metals localization in nerve cells , 2002, Microscopy research and technique.

[3]  P. Iversen,et al.  Expression and regulation of brain metallothionein , 1995, Neurochemistry International.

[4]  S. Choudhuri,et al.  Constitutive expression of metallothionein genes in mouse brain. , 1995, Toxicology and applied pharmacology.

[5]  I. Bièche,et al.  Real-time reverse transcription-PCR assay for future management of ERBB2-based clinical applications. , 1999, Clinical chemistry.

[6]  Weihong Liu,et al.  A new quantitative method of real time reverse transcription polymerase chain reaction assay based on simulation of polymerase chain reaction kinetics. , 2002, Analytical biochemistry.

[7]  Sunanda,et al.  Corticosterone attenuates zinc-induced neurotoxicity in primary hippocampal cultures , 1998, Brain Research.

[8]  M. Aschner,et al.  Roles of the metallothionein family of proteins in the central nervous system , 2001, Brain Research Bulletin.

[9]  H. Jörnvall,et al.  Brain-specific metallothionein-3 has higher metal-binding capacity than ubiquitous metallothioneins and binds metals noncooperatively. , 2002, Biochemistry.

[10]  J. Hidalgo,et al.  Enhanced seizures and hippocampal neurodegeneration following kainic acid‐induced seizures in metallothionein‐I + II‐deficient mice , 2000, The European journal of neuroscience.

[11]  N. Berman,et al.  Chemical modulation of metallothionein I and III mRNA in mouse brain , 1995, Neurochemistry International.

[12]  M. Aschner The functional significance of brain metallothioneins , 1996, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.