Blocking both E-selectin and P-selectin inhibits neutrophil recruitment into the murine testis after ischemia-reperfusion-induced injury


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Celebi M., Paul A. G. A.

ACTA VETERINARIA BRNO, cilt.77, sa.3, ss.321-326, 2008 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 77 Sayı: 3
  • Basım Tarihi: 2008
  • Doi Numarası: 10.2754/avb200877030321
  • Dergi Adı: ACTA VETERINARIA BRNO
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.321-326
  • Anahtar Kelimeler: selectin, neutrophil, testis, murine, torsion, antibody, CELL-SPECIFIC APOPTOSIS, EXPRESSION
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Ondokuz Mayıs Üniversitesi Adresli: Evet

Özet

Ischemia-reperfusion (IR) injury of the testis results in germ cell specific apoptosis, a process in which neutrophil recruitment to the testes plays a critical role. Adhesion molecules, in particular E- and P-selectins, play a critical role in this recruitment. The present study sought to characterize the inhibitory effect of function-blocking monoclonal anti-mouse E- and P-selectin antibodies on the migration of neutrophils into the IR-induced testis of the mouse. Mice were subjected to a 2 hr period of testicular torsion (ischemia) followed by detorsion (reperfusion). Ten minutes after the onset of reperfusion mice received either a mixture of 200 mu g function-blocking monoclonal E-selectin and P-selectin antibody (FBMAb group; 100 mu g; each) intravenously or 200 mu g of isotype-matched control-antibody (IMCAb group). Separate groups of mice underwent sham-operation (SO group) or received 500 ng of TNF alpha (IF group) to induce inflammation. Mice were sacrificed 24 It after reperfusion and testicular interstitial cells were isolated and analyzed for the presence of neutrophils by means of flow cytometry.