<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Shtukmaster, Stella</dc:creator>
  <dc:creator>Narasimhan, Priyanka</dc:creator>
  <dc:creator>El Faitwri, Tehani</dc:creator>
  <dc:creator>Stubbusch, Jutta</dc:creator>
  <dc:creator>Ernsberger, Uwe</dc:creator>
  <dc:creator>Rohrer, Hermann</dc:creator>
  <dc:creator>Unsicker, Klaus</dc:creator>
  <dc:creator>Huber, Katrin</dc:creator>
  <dc:date>2016-04-19</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The neural-crest-derived sympathoadrenal cell lineage gives rise to sympathetic  neurons and to endocrine chromaffin cells of the adrenal medulla. Both cell types  express a largely overlapping set of genes, including those coding for the molecular  machinery related to the synthesis and exocytotic release of catecholamines. During  their early development, sympathetic neurons and chromaffin cells rely on a shared  transcription factor network that controls the establishment of these common features.  Despite many similarities, mature sympathetic neurons and chromaffin cells  significantly differ regarding their morphology and function. Most prominently,  sympathetic neurons possess axons that are absent in mammalian adrenal chromaffin  cells. The molecular mechanism underlying the divergent development of  sympathoadrenal cells into neuronal and endocrine cells remains elusive. Mutational  inactivation of the ribonuclease dicer hints at the importance of microRNAs in this  diversification. We show here that miR-124 is detectable in developing sympathetic  neurons but absent in chromaffin cell precursors. We further demonstrate that miR- 124 promotes neurite elongation when transfected into cultured chromaffin cells  indicating its capability to support the establishment of a neuronal morphology in non- neuronal sympathoadrenal cells. Our results also show that treatment of PC12 cells  with the neurotrophin nerve growth factor leads to an upregulation of miR-124  expression and that inhibition of miR-124 reduces nerve-growth-factor-induced neurite  outgrowth in PC12 cells. Thus, our data indicate that miR-124 contributes to the  establishment of specific neuronal features in developing sympathoadrenal cells.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/305081</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305081/files/hub_mde.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1007/s00441-016-2395-9</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Cell and Tissue Research. - 2016, vol. 365, no. 2, p. 225–232</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">miR-124</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Chromaffin cell</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Sympathoadrenal cell lineage</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Sympathetic neuron</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Mouse</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">MiR-124 is differentially expressed in derivatives of the sympathoadrenal cell lineage and promotes neurite elongation in chromaffin cells</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
