Beta-defensin 22 is a major component of the mouse sperm glycocalyx
| Autor: | Charles L. Bevins, Robert J. Kays, James W. Overstreet, Gary N. Cherr, Cathy A. Treece, Theodore L. Tollner, Ashley I. Yudin |
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| Rok vydání: | 2008 |
| Předmět: |
Male
Embryology endocrine system beta-Defensins Blotting Western Molecular Sequence Data Mice Inbred Strains Glycocalyx Article Andrology Mice Endocrinology Vas Deferens Antigen medicine Animals Amino Acid Sequence RNA Messenger reproductive and urinary physiology Epididymis biology Base Sequence urogenital system Reverse Transcriptase Polymerase Chain Reaction Vas deferens Obstetrics and Gynecology Antibodies Monoclonal Cell Biology Sperm Spermatozoa Blot medicine.anatomical_structure Reproductive Medicine Microscopy Fluorescence biology.protein Oviduct Electrophoresis Polyacrylamide Gel Female Rabbits Antibody Sperm Capacitation Immunostaining |
| Zdroj: | Reproduction (Cambridge, England). 136(6) |
| ISSN: | 1741-7899 |
| Popis: | Surface components of sperm isolated from the cauda epididymides were stabilized by whole sperm fixation for immunization of rabbits. The resulting immunoglobulins (Igs) recognized a single protein of 130 kDa (non-reduced) or 54–57 kDa (reduced) on western blots of cauda sperm. Igs recognized the same 54–57 kDa protein band on whole tissue blots of the corpus and cauda epididymidis and vas deferens. No immunoreactive bands were detected on blots of the prostate, seminal vesicles, testes, caput epididymis, or any of various non-reproductive tissues. Removal of sperm from the vas deferens prior to blotting eliminated the detection of the sperm antigen. Antibodies raised to synthetic peptides, identical in amino acid sequence to two unique spans of DEFB22, recognized the same 130/54–57 kDa antigen on western blots of both caudal sperm and the purified antigen isolated with the anti-sperm Ig. From indirect immunofluorescence, both the anti-sperm and anti-peptide Igs appeared to localize to the entire sperm surface, a pattern confirmed at the ultrastructural level. Real-time PCR identified the corpus epididymides as the major site of expression of DEFB22, with negligible expression in the testes, caput epididymides, and vas deferens. Immunostaining of epididymal sections showed DEFB22 being released into the lumen at the distal caput/proximal corpus, with sperm becoming intensely coated with DEFB22 as they reached the distal corpus. Most uterine sperm recovered from mice 4 h following copulation exhibited DEFB22 coating the entire sperm surface. By contrast, some sperm recovered from the oviduct and cumulus extracellular matrix showed loss of DEFB22 from the sperm head. |
| Databáze: | OpenAIRE |
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