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S100 protein expression in subpopulations of neurons of rat brain

Available data are conflicting as regards the occurrence of Ca 2+ and Zn 2+ binding S100 proteins in neurons of mammalian brain. Here the localization and expression of S100 was re-investigated using several different antibodies and in situ hybridization. A map is provided for the distribution of tw...

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Bibliographic Details
Published in:Neuroscience 1995-08, Vol.67 (4), p.977-991
Main Authors: Rickmann, M., Wolff, J.R.
Format: Article
Language:English
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Summary:Available data are conflicting as regards the occurrence of Ca 2+ and Zn 2+ binding S100 proteins in neurons of mammalian brain. Here the localization and expression of S100 was re-investigated using several different antibodies and in situ hybridization. A map is provided for the distribution of two classes of S100-positive neuron populations in the adult rat CNS. “Persistently S100-positive” neurons had large size, were strongly immunoreactive and were mainly distributed in the nuclei of the lower brainstem and cerebellum. “Variably S100-positive” neurons were preferentially found in the forebrain of rats older than 90 days and were especially numerous in limbic regions. The S100-immunoreactivity in these neurons was moderately intense, occurred with high interindividual variation and appeared related to function as suggested by variations due to anesthesia. The expression of S100 mRNA in neurons was re-investigated at high spatial resolution with non-radioactive in situ hybridization using an oligonucleotide specific for S100β-mRNA. Expression of S100 was demonstrated in astrocytes and in those neuron populations which were also strongly S100-immunoreactive. No expression of S100β message was seen in weakly immunoreactive neurons, but this may be due to low sensitivity of the techniques used. The data suggest that the S100 proteins are synthesized in all astrocytes and in distinct subpopulations of neurons in rat brain. These neurons show a characteristic topography and vary in S100 expression probably due to their function and maturation.
ISSN:0306-4522
1873-7544
DOI:10.1016/0306-4522(94)00615-C