Neuroendocrine Cells

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Jeffrey G Tasker - One of the best experts on this subject based on the ideXlab platform.

  • rapid nongenomic glucocorticoid actions in male mouse hypothalamic Neuroendocrine Cells are dependent on the nuclear glucocorticoid receptor
    Endocrinology, 2015
    Co-Authors: Jebun Nahar, Juhee Haam, Chun Chen, Zhiying Jiang, Nicholas R Glatzer, Louis J Muglia, Gary P Dohanich, James P Herman, Jeffrey G Tasker
    Abstract:

    Corticosteroids act classically via cognate nuclear receptors to regulate gene transcription; however, increasing evidence supports rapid, nontranscriptional corticosteroid actions via activation of membrane receptors. Using whole-cell patch clamp recordings in hypothalamic slices from male mouse genetic models, we tested for nongenomic glucocorticoid actions at glutamate and gamma aminobutyric acid (GABA) synapses in hypothalamic Neuroendocrine Cells, and for their dependence on the nuclear glucocorticoid receptor (GR). In enhanced green fluorescent protein-expressing CRH neurons of the paraventricular nucleus (PVN) and in magnocellular neurons of the PVN and supraoptic nucleus (SON), dexamethasone activated postsynaptic membrane-associated receptors and G protein signaling to elicit a rapid suppression of excitatory postsynaptic inputs, which was blocked by genetic deletion of type I cannabinoid receptors and a type I cannabinoid receptor antagonist. In magnocellular neurons, dexamethasone also elicited...

  • Somato-dendritic mechanisms underlying the electrophysiological properties of hypothalamic magnocellular Neuroendocrine Cells: A multicompartmental model study
    Journal of Computational Neuroscience, 2007
    Co-Authors: Alexander O. Komendantov, Natalia A. Trayanova, Jeffrey G Tasker
    Abstract:

    Magnocellular Neuroendocrine Cells (MNCs) of the hypothalamus synthesize the neurohormones vasopressin and oxytocin, which are released into the blood and exert a wide spectrum of actions, including the regulation of cardiovascular and reproductive functions. Vasopressin- and oxytocin-secreting neurons have similar morphological structure and electrophysiological characteristics. A realistic multicompartmental model of a MNC with a bipolar branching structure was developed and calibrated based on morphological and in vitro electrophysiological data in order to explore the roles of ion currents and intracellular calcium dynamics in the intrinsic electrical MNC properties. The model was used to determine the likely distributions of ion conductances in morphologically distinct parts of the MNCs: soma, primary dendrites and secondary dendrites. While reproducing the general electrophysiological features of MNCs, the model demonstrates that the differential spatial distributions of ion channels influence the functional expression of MNC properties, and reveals the potential importance of dendritic conductances in these properties.

Jaideep S Bains - One of the best experts on this subject based on the ideXlab platform.

Hisatsugu Koshimizu - One of the best experts on this subject based on the ideXlab platform.

  • Biogenesis and Transport of Secretory Granules to Release Site in Neuroendocrine Cells
    Journal of Molecular Neuroscience, 2008
    Co-Authors: Joshua J. Park, Hisatsugu Koshimizu
    Abstract:

    Biogenesis and post-Golgi transport of peptidergic secretory granules to the release site are crucial for secretion of neuropeptides from Neuroendocrine Cells. Recent studies have uncovered multilevel molecular mechanisms for the regulation of secretory granule biogenesis. Insulinoma-associated protein 2 (ICA512/IA-2), polypyrimidine-tract binding protein, and chromogranin A have been identified to regulate secretory granule biogenesis at the transcriptional, posttranscriptional, and posttranslational levels, respectively, by increasing granule protein levels, which in turn drives granule formation after stimulation. Post-Golgi transport of secretory granules is microtubule-based and mediated by transmembrane carboxypeptidase E (CPE). The cytoplasmic tail of CPE anchors secretory granules to the microtubule motors, kinesin-2 and -3, or dynein, via interaction with the adaptor, dynactin, to mediate anterograde and retrograde transport, respectively.

Kari Alitalo - One of the best experts on this subject based on the ideXlab platform.

  • vegf c and vegf d expression in Neuroendocrine Cells and their receptor vegfr 3 in fenestrated blood vessels in human tissues
    The FASEB Journal, 2000
    Co-Authors: Taina A Partanen, Johanna Arola, Anne Saaristo, Lotta Jussila, Ari Ora, Markku Miettinen, Steven A Stacker, Marc G Achen, Kari Alitalo
    Abstract:

    Recently, vascular endothelial growth factor receptor 3 (VEGFR-3) has been shown to provide a specific marker for lymphatic endothelia in certain human tissues. In this study, we have investigated the expression of VEGFR-3 and its ligands VEGF-C and VEGF-D in fetal and adult tissues. VEGFR-3 was consistently detected in the endothelium of lymphatic vessels such as the thoracic duct, but fenestrated capillaries of several organs including the bone marrow, splenic and hepatic sinusoids, kidney glomeruli and endocrine glands also expressed this receptor. VEGF-C and VEGF-D, which bind both VEGFR-2 and VEGFR-3 were expressed in vascular smooth muscle Cells. In addition, intense cytoplasmic staining for VEGF-C was observed in Neuroendocrine Cells such as the α Cells of the islets of Langerhans, prolactin secreting Cells of the anterior pituitary, adrenal medullary Cells, and dispersed Neuroendocrine Cells of the gastrointestinal tract. VEGF-D was observed in the innermost zone of the adrenal cortex and in certa...

Jeffrey I Gordon - One of the best experts on this subject based on the ideXlab platform.

  • a transgenic mouse model of metastatic prostate cancer originating from Neuroendocrine Cells
    Proceedings of the National Academy of Sciences of the United States of America, 1998
    Co-Authors: Emily M Garabedian, Peter A Humphrey, Jeffrey I Gordon
    Abstract:

    A transgenic mouse model of metastatic prostate cancer has been developed that is 100% penetrant in multiple pedigrees. Nucleotides −6500 to +34 of the mouse cryptdin-2 gene were used to direct expression of simian virus 40 T antigen to a subset of Neuroendocrine Cells in all lobes of the FVB/N mouse prostate. Transgene expression is initiated between 7 and 8 weeks of age and leads to development of prostatic intraepithelial neoplasia within a week. Prostatic intraepithelial neoplasia progresses rapidly to local invasion. Metastases to lymph nodes, liver, lung, and bone are common by 6 months. Tumorigenesis is not dependent on androgens. This model indicates that the Neuroendocrine cell lineage of the prostate is exquisitely sensitive to transformation and provides insights about the significance of Neuroendocrine differentiation in human prostate cancer.