Subcellular localization of specific mRNAs and their protein products in Purkinje cells by combined fluorescence in situ hybridization and immunocytochemistry (original) (raw)
Abstract
In this study we have investigated the subcellular distribution of two mRNAs coding for the Purkinje cell-specific proteins, calbindin D28K and L7 (L7/pcp-2). Whereas calbindin mRNA was found to be in the cell body only, L7 transcripts could be detected within the molecular layer, corresponding to Purkinje cell dendrites. We have now combined a highly sensitive fluorescence-based in situ hybridization protocol with immunofluorescence in conjunction with confocal optical sectioning to analyze the precise localization of these mRNAs in individual Purkinje neurons. We show that L7 mRNA is localized in clusters within the proximal and distal branches of dendrites, but also in the proximal part of Purkinje cell axons. In contrast, calbindin transcripts are restricted to the axonal pole of the perikaryon. Purkinje cells grown in primary cultures reveal similar mRNA distribution patterns for the two transcripts. Thus, the mechanism underlying localization of mRNA within Purkinje cells seems to function in a cell-intrinsic manner, guiding specific transcripts, such as L7 mRNA, to neuronal processes while restricting others, such as calbindin mRNA, to the perikaryon.
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Authors and Affiliations
- Abteilung Anatomie und Zellbiologie, der Universität Ulm, Albert-Einstein-Allee 11, D-89081 Ulm, Germany Tel. ++49-731-502-3224; Fax ++49-731-502-3217; e-mail Karl.Schilling@medizin.uni-ulm.de, , , , , , DE
I. Wanner, Stephan L. Baader, Manfred Brich & K. Schilling - Department of Cell Biology, Neurobiology and Anatomy, and Neurobiotechnology Center, The Ohio State University, Columbus, OH (JO), , , , ,
John Oberdick
Authors
- I. Wanner
- Stephan L. Baader
- Manfred Brich
- John Oberdick
- K. Schilling
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Accepted: 24 July 1997
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Wanner, I., Baader, S., Brich, M. et al. Subcellular localization of specific mRNAs and their protein products in Purkinje cells by combined fluorescence in situ hybridization and immunocytochemistry.Histochemistry 108, 345–357 (1997). https://doi.org/10.1007/s004180050175
- Issue date: October 1997
- DOI: https://doi.org/10.1007/s004180050175