<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>Nazıroğlu, Mustafa</dc:creator>
  <dc:creator>Çiğ, Bilal</dc:creator>
  <dc:creator>Yazğan, Yener</dc:creator>
  <dc:creator>Schwaerzer, Gerburg K.</dc:creator>
  <dc:creator>Theilig, Franziska</dc:creator>
  <dc:creator>Pecze, László</dc:creator>
  <dc:date>2019-08-27</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">In proteinuric nephropathies of chronic kidney disease, the epithelial cells of the  nephron including the collecting duct are exposed to high concentrations of luminal  albumin. Albumin is taken up from collecting duct cells by endocytosis causing  excessive reactive oxygen species (ROS) production and a proinflammatory  response. Curcumin used in the traditional medicine possesses anti-inflammatory and  antioxidant effects. ROS and ADP-ribose (ADPR) activate the cation channel TRPM2.  We hypothesize, that albumin-induced cell stress and proinflammatory response are  mediated by Ca2+ and can be reduced by curcumin. The cortical collecting duct  (CCD) cells mpkCCDc14 exhibit spontaneous and inducible Ca2+ oscillations, which  can be blocked by pre-treatment with curcumin. Curcumin accumulates in plasma  membrane and intracellular vesicles, where it interferes with TRPM2 and decreases  the influx of Ca2+. Albumin reduces cell viability and increases apoptosis, NF-κB  activation, and mitochondrial membrane depolarization via Ca2+-dependent signaling,  which results in increased ROS production. Albumin-induced cell stress is diminished  by the inhibition of TRPM2 after administration of curcumin and ADPR (PARP1)  inhibitors. Curcumin did not reduce the Ca2+ elevation induced by thapsigargin in  Ca2+-free medium, but it reduced the function of store-operated Ca2+ channels and  ATP-evoked Ca2+ response. In conclusion, albumin-induced oxidative stress is  mediated by Ca2+-dependent signaling via TRPM2 and leads to cell damage and a  proinflammatory response, strengthening the role of CCD cells in the progression of  chronic kidney disease.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308248</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308248/files/pec_aec.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1038/s41598-019-48716-x</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Scientific Reports. - 2019, vol. 9, no. 1, p. 1–16</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Albumin evokes Ca 2+ -induced cell oxidative stress and apoptosis through TRPM2 channel in renal collecting duct cells reduced by curcumin</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
