<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>Wehrli, Philipp</dc:creator>
  <dc:creator>Loffing-Cueni, Dominique</dc:creator>
  <dc:creator>Kaissling, Brigitte</dc:creator>
  <dc:creator>Loffing, Johannes</dc:creator>
  <dc:date>2006-12-22</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The renal collecting system (CS) is composed of segment-specific (SS) and  intercalated (IC) cells. The latter comprise at least two subtypes (type A and  non-type A IC). The origin and maintenance of cellular heterogeneity in the  CS is unclear. Among other hypotheses, it was proposed that one subtype of  IC cells represents a stem cell population from which all cell types in the CS  may arise. In the present study, we tested this stem cell hypothesis for the  adult kidney by assessing DNA synthesis as a marker for cell replication. SS  and IC cells were identified by their characteristic expressions of sodium-  (epithelial sodium channel, Na–K-ATPase), water- (aquaporin-2) and  acid/base- (H⁺-ATPase, anion exchanger AE1) transporting proteins.  Immunostaining for bromodeoxyuridine (BrdU) and for the proliferating cell  nuclear antigen (PCNA) was used to reveal DNA synthesis in CS epithelium.  BrdU- and PCNA-immunostaining as well as mitotic figures were seen in all  subtypes of CS cells. Dividing cells retained the cell-type specific expression  of marker molecules. Treatment of mice with bumetanide combined with a  high oral salt intake, which increases the tubular salt load in the CS,  profoundly increased the DNA-synthesis rate in SS and non-type A IC cells,  but reduced it in type A IC cells. Thus, our data show that DNA synthesis  and cell replication occur in each cell lineage of the CS and in differentiated  cells. The replication rate in each cell type can be differently modulated by  functional stimulation. Independent proliferation of each cell lineage might  contribute to maintain the cellular heterogeneity of the CS of the adult kidney  and may also add to the adaptation of the CS to altered functional  requirements.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/300363</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/300363/files/418_2006_Article_261.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1007/s00418-006-0261-7</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Histochemistry and Cell Biology. - 2007, vol. 127, no. 4, p. 389-398</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Principal cells</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">intercalated cells</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">differentiation</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">H⁺-ATPase</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">ENaC</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Replication of segment-specific and intercalated cells in the mouse renal collecting system</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
