<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>Dressen, Cindy</dc:creator>
  <dc:creator>Schwaller, Beat</dc:creator>
  <dc:creator>Vegh, Grégory</dc:creator>
  <dc:creator>Leleux, Fabienne</dc:creator>
  <dc:creator>Gall, David</dc:creator>
  <dc:creator>Lebrun, Philippe</dc:creator>
  <dc:creator>Lybaert, Pascale</dc:creator>
  <dc:date>2018-09-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Calretinin has been detected in various excitable cells but the presence and putative  roles of such a calcium-binding protein has never been characterized in  sperm.Epididymal spermatozoa were collected from C57Bl6 (wild-type, WT) or  calretinin knockout (CR−/−) mice and Wistar rats. A specific staining for calretinin was  detected by immunofluorescence in the principal piece of the flagellum, both in WT  mouse and rat spermatozoa. Western blots confirmed the expression of calretinin in  rat and WT spermatozoa as well as its absence in CR−/− mice.No significant  difference was observed in the spontaneous acrosome reaction between WT and  CR−/− sperm. The addition of the calcium-ionophore A-23187, Thapsigargin or  Progesterone to WT or CR−/− incubated spermatozoa induced increases in the  acrosome reaction but the stimulatory effects were identical in both genotypes. Motility  measurements assessed by computer-assisted sperm analysis indicated that, under  basal non-stimulatory conditions, CR-/- sperm exhibited a lower curvilinear velocity  and a smaller lateral head movement amplitude, although no difference was observed  for the beat cross frequency. After incubation with 25 mM NH4Cl, the curvilinear  velocity, the amplitude of the lateral head movement and the hyperactivation were  increased, while the beat cross frequency was decreased, in both  genotypes.Evaluation of the in vivo fertility potential indicated that the CR−/− litter  sizes were clearly reduced compared to the WT litter sizes.Our study describes, for  the first time, the expression of calretinin in sperm. These data extend the potential  implication of calcium-binding proteins in the sperm calcium-signaling cascade and  bring new insights into the understanding of sperm physiology.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307287</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307287/files/sch_cpr.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307287/files/sch_cpr_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ceca.2018.05.008</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Cell Calcium. - 2018, vol. 74, p. 94–101</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Characterization and potential roles of calretinin in rodent spermatozoa</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
