#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Partial Deletion of Chromosome 8 β-defensin Cluster Confers Sperm Dysfunction and Infertility in Male Mice


β-defensin peptides are a family of antimicrobial peptides present at mucosal surfaces, with the main site of expression under normal conditions in the male reproductive tract. Although they kill microbes in vitro and interact with immune cells, the precise role of these genes in vivo remains uncertain. We show here that homozygous deletion of a cluster of nine β-defensin genes (DefbΔ9) in the mouse results in male sterility. The sperm derived from the mutants have reduced motility and increased fragility. Epididymal sperm isolated from the cauda should require capacitation to induce the acrosome reaction but sperm from the mutants demonstrate precocious capacitation and increased spontaneous acrosome reaction compared to wild-types but have reduced ability to bind the zona pellucida of oocytes. Ultrastructural examination reveals a defect in microtubule structure of the axoneme with increased disintegration in mutant derived sperm present in the epididymis cauda region, but not in caput region or testes. Consistent with premature acrosome reaction, sperm from mutant animals have significantly increased intracellular calcium content. Thus we demonstrate in vivo that β-defensins are essential for successful sperm maturation, and their disruption leads to alteration in intracellular calcium, inappropriate spontaneous acrosome reaction and profound male infertility.


Vyšlo v časopise: Partial Deletion of Chromosome 8 β-defensin Cluster Confers Sperm Dysfunction and Infertility in Male Mice. PLoS Genet 9(10): e32767. doi:10.1371/journal.pgen.1003826
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003826

Souhrn

β-defensin peptides are a family of antimicrobial peptides present at mucosal surfaces, with the main site of expression under normal conditions in the male reproductive tract. Although they kill microbes in vitro and interact with immune cells, the precise role of these genes in vivo remains uncertain. We show here that homozygous deletion of a cluster of nine β-defensin genes (DefbΔ9) in the mouse results in male sterility. The sperm derived from the mutants have reduced motility and increased fragility. Epididymal sperm isolated from the cauda should require capacitation to induce the acrosome reaction but sperm from the mutants demonstrate precocious capacitation and increased spontaneous acrosome reaction compared to wild-types but have reduced ability to bind the zona pellucida of oocytes. Ultrastructural examination reveals a defect in microtubule structure of the axoneme with increased disintegration in mutant derived sperm present in the epididymis cauda region, but not in caput region or testes. Consistent with premature acrosome reaction, sperm from mutant animals have significantly increased intracellular calcium content. Thus we demonstrate in vivo that β-defensins are essential for successful sperm maturation, and their disruption leads to alteration in intracellular calcium, inappropriate spontaneous acrosome reaction and profound male infertility.


Zdroje

1. SchutteBC, MitrosJP, BartlettJA, WaltersJD, JiaHP, et al. (2002) Discovery of five conserved beta -defensin gene clusters using a computational search strategy. Proc Natl Acad Sci USA 99: 2129–2133.

2. PatilAA, CaiY, SangY, BlechaF, ZhangG (2005) Cross-species analysis of the mammalian β-defensin gene family: presence of syntenic gene clusters and preferential expression in the male reproductive tract. Physiological Genomics 23: 5–17.

3. AbuBS, HolloxEJ, ArmourJA (2009) Allelic recombination between distinct genomic locations generates copy number diversity in human beta-defensins. Proc Natl Acad Sci USA 106: 853–858.

4. HolloxEJ, HuffmeierU, ZeeuwenPL, PallaR, LascorzJ, et al. (2008) Psoriasis is associated with increased beta-defensin genomic copy number. Nat Genet 40: 23–25.

5. SempleCA, MaxwellA, GautierP, KilanowskiFM, EastwoodH, et al. (2005) The complexity of selection at the major primate beta-defensin locus. BMC Evol Biol 5: 32.

6. SempleF, DorinJR (2012) beta-Defensins: multifunctional modulators of infection, inflammation and more? J Innate Immun 4: 337–348.

7. YamaguchiY, NagaseT, MakitaR, FukuharaS, TomitaT, et al. (2002) Identification of multiple novel epididymis-specific beta-defensin isoforms in humans and mice. J Immunol 169: 2516–2523.

8. ZaballosA, VillaresR, AlbarJP, MartinezA, MarquezG (2004) Identification on mouse chromosome 8 of new beta-defensin genes with regionally specific expression in the male reproductive organ. J Biol Chem 279: 12421–12426.

9. ZhouCX, ZhangYL, XiaoL, ZhengM, LeungKM, et al. (2004) An epididymis-specific beta-defensin is important for the initiation of sperm maturation. Nat Cell Biol 6: 458–464.

10. JohnstonDS, TurnerTT, FingerJN, OwtscharukTL, KopfGS, et al. (2007) Identification of epididymis-specific transcripts in the mouse and rat by transcriptional profiling. Asian J Androl 9: 522–527.

11. YudinAI, TreeceCA, TollnerTL, OverstreetJW, CherrGN (2005) The carbohydrate structure of DEFB126, the major component of the cynomolgus Macaque sperm plasma membrane glycocalyx. J Membr Biol 207: 119–129.

12. ZhaoY, DiaoH, NiZ, HuS, YuH, et al. (2011) The epididymis-specific antimicrobial peptide beta-defensin 15 is required for sperm motility and male fertility in the rat (Rattus norvegicus) 3. Cell MolLife Sci 68: 697–708.

13. TollnerTL, VennersSA, HolloxEJ, YudinAI, LiuX, et al. (2011) A Common Mutation in the Defensin DEFB126 Causes Impaired Sperm Function and Subfertility. Sci Transl Med 3: 92ra65.

14. MorrisonG, KilanowskiF, DavidsonD, DorinJ (2002) Characterization of the mouse Beta defensin 1, defb1, mutant mouse model. Infect Immun 70: 3053–3060.

15. MoserC, WeinerDJ, LysenkoE, BalsR, WeiserJN, et al. (2002) beta-Defensin 1 contributes to pulmonary innate immunity in mice. Infect Immun 70: 3068–3072.

16. AdamsDJ, BiggsPJ, CoxT, DaviesR, van derWL, et al. (2004) Mutagenic insertion and chromosome engineering resource (MICER) 15. Nat Genet 36: 867–871.

17. LangeUC, AdamsDJ, LeeC, BartonS, SchneiderR, et al. (2008) Normal germ line establishment in mice carrying a deletion of the Ifitm/Fragilis gene family cluster. Mol Cell Biol 28: 4688–4696.

18. SempleC, RolfeM, DorinJ (2003) Duplication and selection in the evolution of primate beta-defensin genes. Genome Biology 4: R31.

19. SchroederBO, WuZ, NudingS, GroscurthS, MarcinowskiM, et al. (2011) Reduction of disulphide bonds unmasks potent antimicrobial activity of human beta-defensin 1. Nature 469: 419–423.

20. PublicoverS, HarperCV, BarrattC (2007) [Ca2+]i signalling in sperm–making the most of what you've got. Nat Cell Biol 9: 235–242.

21. FraserLR (1993) In-Vitro Capacitation and Fertilization. Guide to Techniques in Mouse Development 225: 239–253.

22. TaoJ, CritserES, CritserJK (1993) Evaluation of mouse sperm acrosomal status and viability by flow cytometry. Mol Reprod Dev 36: 183–194.

23. TardifS, CormierN (2011) Role of zonadhesin during sperm-egg interaction: a species-specific acrosomal molecule with multiple functions. Mol Hum Reprod 17: 661–668.

24. OliveiraH, SpanòM, SantosC, PereiraMeL (2009) Adverse effects of cadmium exposure on mouse sperm. Reprod Toxicol 28: 550–555.

25. JinM, FujiwaraE, KakiuchiY, OkabeM, SatouhY, et al. (2011) Most fertilizing mouse spermatozoa begin their acrosome reaction before contact with the zona pellucida during in vitro fertilization. Proc Natl Acad Sci USA 108: 4892–4896.

26. InoueN, SatouhY, IkawaM, OkabeM, YanagimachiR (2011) Acrosome-reacted mouse spermatozoa recovered from the perivitelline space can fertilize other eggs. Proc Natl Acad Sci USA 108: 20008–20011.

27. KrutskikhA, PoliandriA, Cabrera-SharpV, DacheuxJL, PoutanenM, et al. (2012) Epididymal protein Rnase10 is required for post-testicular sperm maturation and male fertility. FASEB J 26: 4198–4209.

28. TurunenHT, SipilaP, KrutskikhA, ToivanenJ, MankonenH, et al. (2012) Loss of cysteine-rich secretory protein 4 (Crisp4) leads to deficiency in sperm-zona pellucida interaction in mice. Biol Reprod 86: 1–8.

29. LesichKA, KelschCB, PonichterKL, DionneBJ, DangL, et al. (2012) The calcium response of mouse sperm flagella: role of calcium ions in the regulation of dynein activity. Biol Reprod 86: 105.

30. SatoH, TaketomiY, IsogaiY, MikiY, YamamotoK, et al. (2010) Group III secreted phospholipase A2 regulates epididymal sperm maturation and fertility in mice. J Clin Invest 120: 1400–1414.

31. LaineVJ, GrassDS, NevalainenTJ (2000) Resistance of transgenic mice expressing human group II phospholipase A2 to Escherichia coli infection. Infect Immun 68: 87–92.

32. LishkoPV, KirichokY (2010) The role of Hv1 and CatSper channels in sperm activation. J Physiol 588: 4667–4672.

33. WeissgerberP, KriebsU, TsvilovskyyV, OlaussonJ, KretzO, et al. (2011) Male fertility depends on Ca2+ absorption by TRPV6 in epididymal epithelia. Sci Signal 4: ra27.

34. TanphaichitrN, HansenC (1994) Production of motile acrosome-reacted mouse sperm with nanomolar concentration of calcium ionophore A23187. Molecular Reproduction and Development 37: 326–334.

35. SpelbrinkRG, DilmacN, AllenA, SmithTJ, ShahDM, et al. (2004) Differential antifungal and calcium channel-blocking activity among structurally related plant defensins. Plant Physiol 135: 2055–2067.

36. ZalazarL, Saez LancellottiTE, ClementiM, LombardoC, LamattinaL, et al. (2012) SPINK3 modulates mouse sperm physiology through the reduction of nitric oxide level independently of its trypsin inhibitory activity. Reproduction 143: 281–295.

37. HardwickRJ, MachadoLR, ZuccheratoLW, AntolinosS, XueY, et al. (2011) A worldwide analysis of beta-defensin copy number variation suggests recent selection of a high-expressing DEFB103 gene copy in East Asia. Hum Mutat 32: 743–750.

38. WiserA, SacharS, GhetlerY, ShulmanA, BreitbartH (2013) Assessment of sperm hyperactivated motility and acrosome reaction can discriminate the use of spermatozoa for conventional in vitro fertilisation or intracytoplasmic sperm injection: Preliminary results. Andrologia doi: 10.1111/and.12068

39. ShanahanMT, TanabeH, OuelletteAJ (2011) Strain-specific polymorphisms in Paneth cell α-defensins of C57BL/6 mice and evidence of vestigial myeloid α-defensin pseudogenes. Infect Immun 79: 459–473.

40. ChomczynskiP, SacchiN (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Bio chem 162: 156–159.

41. TardifS, SirardMA, SullivanR, BaileyJL (1999) Identification of capacitation-associated phosphoproteins in porcine sperm electroporated with ATP-gamma-(32)P. Mol Reprod Dev 54: 292–302.

42. TardifS, WilsonMD, WagnerR, HuntP, GertsensteinM, et al. (2010) Zonadhesin is essential for species specificity of sperm adhesion to the egg zona pellucida. J Biol Chem 285: 24863–24870.

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2013 Číslo 10
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Aktuální možnosti diagnostiky a léčby litiáz
nový kurz
Autori: MUDr. Tomáš Ürge, PhD.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#