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Vol. 20, Issue 7, 2108-2120, April 1, 2009
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*Department of Physiology and Neurobiology, Eötvös Loránd University, Budapest, Hungary H-1117;
Institute of Cell Biology and Immunology, University Stuttgart, D-70569 Stuttgart, Germany; and
Brain Research Institute, Medical Faculty of University of Zürich, CH-8057 Zürich, Switzerland, and Department of Biology of the Swiss Federal Institute of Technology, CH-8092 Zürich, Switzerland
Submitted September 19, 2008;
Revised December 22, 2008;
Accepted February 2, 2009
Monitoring Editor: Vivek Malhotra
Protein kinase D (PKD) is known to participate in various cellular functions, including secretory vesicle fission from the Golgi and plasma membrane-directed transport. Here, we report on expression and function of PKD in hippocampal neurons. Expression of an enhanced green fluorescent protein (EGFP)-tagged PKD activity reporter in mouse embryonal hippocampal neurons revealed high endogenous PKD activity at the Golgi complex and in the dendrites, whereas PKD activity was excluded from the axon in parallel with axonal maturation. Expression of fluorescently tagged wild-type PKD1 and constitutively active PKD1S738/742E (caPKD1) in neurons revealed that both proteins were slightly enriched at the trans-Golgi network (TGN) and did not interfere with its thread-like morphology. By contrast, expression of dominant-negative kinase inactive PKD1K612W (kdPKD1) led to the disruption of the neuronal Golgi complex, with kdPKD1 strongly localized to the TGN fragments. Similar findings were obtained from transgenic mice with inducible, neuron-specific expression of kdPKD1-EGFP. As a prominent consequence of kdPKD1 expression, the dendritic tree of transfected neurons was reduced, whereas caPKD1 increased dendritic arborization. Our results thus provide direct evidence that PKD activity is selectively involved in the maintenance of dendritic arborization and Golgi structure of hippocampal neurons.
Address correspondence to: Katalin Schlett (schlettk{at}ludens.elte.hu)
Abbreviations used: diC8, 1,2-dioctanoylglycerol; DIV, days in vitro; Dox, doxycycline; PDBu, phorbol 12,13-dibutyrate; PI4KIIIβ, phosphatidylinositol 4-kinase IIIβ; PKD, protein kinase D; TGN, trans-Golgi network; VAMP4, vesicle-associated membrane protein 4.
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