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Biology of Reproduction 65, 718-725 (2001)
© 2001 Society for the Study of Reproduction, Inc.


Regular Article

Essential Role of Neutrophils in Germ Cell-Specific Apoptosis Following Ischemia/Reperfusion Injury of the Mouse Testis1

Jeffrey J. Lysiak2,a, Stephen D. Turnera, Quoc An T. Nguyena, Kai Singbartlc, Klaus Leyc, and Terry T. Turnera,b

a Departments of Urology, b Cell Biology c Biomedical Engineering, The University of Virginia Health Science Center, Charlottesville, Virginia 22908

ABSTRACT

This study investigates the role of neutrophils in ischemia-induced aspermatogenesis in the mouse. Previous studies in the rat have demonstrated that ischemia-inducing testicular torsion followed by torsion repair and reperfusion resulted in germ cell-specific apoptosis. This was correlated with an increase in neutrophil adhesion to subtunical venules, an increase in reactive oxygen species, and increased expression of several apoptosis-associated molecules. In the present investigation, wild-type C57BL/6 mice were subjected to various degrees and duration of testicular torsion. A torsion of 720° for 2 h caused disruption of the seminiferous epithelium and significantly reduced testis weight and daily sperm production. An immunohistochemical method specific for apoptotic nuclei indicated that these effects were due to germ cell-specific apoptosis. An increase in myeloperoxidase (MPO) activity and an increase in the number of neutrophils adhering to testicular subtunical venules after torsion repair/reperfusion demonstrated an increase in neutrophil recruitment to the testis. In contrast, E-selectin knockout mice and wild-type mice rendered neutropenic showed a significant decrease in neutrophil recruitment as evidenced by MPO activity and microscopic examination of subtunical venules. Importantly, germ cell-specific apoptosis was also reduced. Thus, germ cell-specific apoptosis is observed after ischemia/reperfusion of the murine testis, and this apoptosis is directly linked to the recruitment of neutrophils to subtunical venules. Endothelial cell adhesion molecules, particularly E-selectin, play an important role in mediating this pathology.

FOOTNOTES

First decision: 23 February 2001.

1 Supported by the National Institutes of Health, grants R01-DK-53072 to T.T.T and HL 54136 to K.L. This work was supported in part by a grant from the A.F.U.D./AUA Research Scholar Program to J.J.L.

2 Correspondence: Jeffrey J. Lysiak, Department of Urology, Box 800422, University of Virginia Health Science Center, Charlottesville, VA 22908. FAX: 804 924 8311; jl6n{at}virginia.edu




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