3D in situ imaging of female reproductive tract reveals molecular signatures of fertilizing spermatozoa in mice

Out of millions of ejaculated sperm, only a few reach the fertilization site in mammals. Flagellar Ca2+ signaling nanodomains, organized by multi-subunit CatSper calcium channel complexes, are pivotal for sperm migration in the female tract, implicating CatSper-dependent mechanisms in sperm selection. Here, using biochemical and pharmacological studies, we demonstrate that CatSper1 is an O-linked glycosylated protein, undergoing capacitation-induced processing dependent on Ca2+ and phosphorylation cascades. CatSper1 processing correlates with protein tyrosine phosphorylation (pY) development in sperm cells capacitated in vitro and in vivo. Using 3D in situ molecular imaging and ANN-based automatic detection of sperm distributed along the cleared female tract, we demonstrate that all spermatozoa past the UTJ possess intact CatSper1 signals. Together, we reveal that fertilizing mouse spermatozoa in situ are characterized by intact CatSper channel, lack of pY, and reacted acrosomes. These findings provide molecular insight into sperm selection for successful fertilization in the female reproductive tract.

[1]  tyrosine kinase , 2020, Catalysis from A to Z.

[2]  P. Lishko,et al.  Dissecting the signaling pathways involved in the function of sperm flagellum. , 2020, Current opinion in cell biology.

[3]  R. Yanagimachi,et al.  Active peristaltic movements and fluid production of the mouse oviduct: their roles in fluid and sperm transport and fertilization† , 2019, Biology of Reproduction.

[4]  S. Gygi,et al.  Dual Sensing of Physiologic pH and Calcium by EFCAB9 Regulates Sperm Motility , 2019, Cell.

[5]  V. del Pozo,et al.  Aspirin desensitization in aspirin-exacerbated respiratory disease: New insights into the molecular mechanisms. , 2018, Respiratory medicine.

[6]  M. Buffone,et al.  Molecular Basis of Human Sperm Capacitation , 2018, Front. Cell Dev. Biol..

[7]  M. Buffone,et al.  Disruption of protein kinase A localization induces acrosomal exocytosis in capacitated mouse sperm , 2018, The Journal of Biological Chemistry.

[8]  M. Ikawa,et al.  Factors controlling sperm migration through the oviduct revealed by gene-modified mouse models , 2018, Experimental animals.

[9]  Q. Shen,et al.  Phosphorylation regulated by protein kinase A and alkaline phosphatase play positive roles in μ-calpain activity. , 2018, Food chemistry.

[10]  J. N. Hansen,et al.  Shedding light on the role of cAMP in mammalian sperm physiology , 2017, Molecular and Cellular Endocrinology.

[11]  D. Clapham,et al.  CatSperζ regulates the structural continuity of sperm Ca2+ signaling domains and is required for normal fertility , 2017, eLife.

[12]  H. Sorimachi,et al.  Calpain research for drug discovery: challenges and potential , 2016, Nature Reviews Drug Discovery.

[13]  Woong Sun,et al.  Corrigendum: ACT-PRESTO: Rapid and consistent tissue clearing and labeling method for 3-dimensional (3D) imaging , 2016, Scientific Reports.

[14]  M. Okabe,et al.  The Behavior and Acrosomal Status of Mouse Spermatozoa In Vitro, and Within the Oviduct During Fertilization after Natural Mating1 , 2016, Biology of reproduction.

[15]  P. Greer,et al.  The tyrosine kinase FER is responsible for the capacitation-associated increase in tyrosine phosphorylation in murine sperm , 2016, Development.

[16]  P. Morales,et al.  Regulation of Sperm Capacitation by the 26S Proteasome: An Emerging New Paradigm in Spermatology1 , 2016, Biology of reproduction.

[17]  P. Gagneux,et al.  Sialylation Facilitates the Maturation of Mammalian Sperm and Affects Its Survival in Female Uterus , 2016, Biology of reproduction.

[18]  T. Baba,et al.  Surfing and Swimming of Ejaculated Sperm in the Mouse Oviduct1 , 2016, Biology of reproduction.

[19]  M. Ikawa,et al.  Behavior of Mouse Spermatozoa in the Female Reproductive Tract from Soon after Mating to the Beginning of Fertilization1 , 2016, Biology of reproduction.

[20]  Yu Jin Jang,et al.  ACT-PRESTO: Rapid and consistent tissue clearing and labeling method for 3-dimensional (3D) imaging , 2016, Scientific Reports.

[21]  Kwanghun Chung,et al.  Simple, Scalable Proteomic Imaging for High-Dimensional Profiling of Intact Systems , 2015, Cell.

[22]  Nicolas Garrido,et al.  Sperm selection in natural conception: what can we learn from Mother Nature to improve assisted reproduction outcomes? , 2015, Human reproduction update.

[23]  S. Kölle Transport, Distribution and Elimination of Mammalian Sperm Following Natural Mating and Insemination. , 2015, Reproduction in domestic animals = Zuchthygiene.

[24]  A. Salicioni,et al.  Biphasic Role of Calcium in Mouse Sperm Capacitation Signaling Pathways , 2015, Journal of cellular physiology.

[25]  Rajan P Kulkarni,et al.  Single-Cell Phenotyping within Transparent Intact Tissue through Whole-Body Clearing , 2014, Cell.

[26]  Steven P. Gygi,et al.  Structurally Distinct Ca2+ Signaling Domains of Sperm Flagella Orchestrate Tyrosine Phosphorylation and Motility , 2014, Cell.

[27]  R. Aitken,et al.  Oxidative stress, spermatozoa and leukocytic infiltration: relationships forged by the opposing forces of microbial invasion and the search for perfection. , 2013, Journal of reproductive immunology.

[28]  A. Darszon,et al.  Ca2+ ionophore A23187 can make mouse spermatozoa capable of fertilizing in vitro without activation of cAMP-dependent phosphorylation pathways , 2013, Proceedings of the National Academy of Sciences.

[29]  F. García-Vázquez,et al.  Boar sperm tyrosine phosphorylation patterns in the presence of oviductal epithelial cells: in vitro, ex vivo, and in vivo models. , 2013, Reproduction.

[30]  Aaron S. Andalman,et al.  Structural and molecular interrogation of intact biological systems , 2013, Nature.

[31]  P. Gagneux,et al.  Sialidases on Mammalian Sperm Mediate Deciduous Sialylation during Capacitation , 2012, The Journal of Biological Chemistry.

[32]  S. Suarez,et al.  Unexpected Flagellar Movement Patterns and Epithelial Binding Behavior of Mouse Sperm in the Oviduct1 , 2012, Biology of reproduction.

[33]  R. Aitken,et al.  Phosphoinositide 3-kinase signalling pathway involvement in a truncated apoptotic cascade associated with motility loss and oxidative DNA damage in human spermatozoa. , 2011, The Biochemical journal.

[34]  M. Okabe,et al.  Most fertilizing mouse spermatozoa begin their acrosome reaction before contact with the zona pellucida during in vitro fertilization , 2011, Proceedings of the National Academy of Sciences.

[35]  D. Clapham,et al.  A Novel Gene Required for Male Fertility and Functional CATSPER Channel Formation in Spermatozoa , 2011, Nature communications.

[36]  A. Wehrend,et al.  Ciliary Transport, Gamete Interaction, and Effects of the Early Embryo in the Oviduct: Ex Vivo Analyses Using a New Digital Videomicroscopic System in the Cow1 , 2009, Biology of reproduction.

[37]  M. Ikawa,et al.  Disruption of ADAM3 Impairs the Migration of Sperm into Oviduct in Mouse1 , 2009, Biology of reproduction.

[38]  S. Suarez,et al.  CatSper-null mutant spermatozoa are unable to ascend beyond the oviductal reservoir. , 2009, Reproduction, fertility, and development.

[39]  G. Cornwall New insights into epididymal biology and function. , 2008, Human reproduction update.

[40]  D. A. O’Brien,et al.  Bicarbonate‐Induced phosphorylation of p270 protein in mouse sperm by cAMP‐Dependent protein kinase , 2008, Molecular reproduction and development.

[41]  R. Aitken,et al.  New insights into the molecular mechanisms of sperm-egg interaction , 2007, Cellular and Molecular Life Sciences.

[42]  D. Clapham,et al.  All four CatSper ion channel proteins are required for male fertility and sperm cell hyperactivated motility , 2007, Proceedings of the National Academy of Sciences.

[43]  Jeff G. Wang,et al.  In vitro fertilization (IVF): a review of 3 decades of clinical innovation and technological advancement , 2006, Therapeutics and clinical risk management.

[44]  P. Brown,et al.  Calpain 11 is unique to mouse spermatogenic cells , 2006, Molecular reproduction and development.

[45]  N. Tonks Redox Redux: Revisiting PTPs and the Control of Cell Signaling , 2005, Cell.

[46]  D. E. Goll,et al.  The calpain system. , 2003, Physiological reviews.

[47]  D. P. Tulsiani Glycan modifying enzymes in luminal fluid of rat epididymis: Are they involved in altering sperm surface glycoproteins during maturation? , 2003, Microscopy research and technique.

[48]  A. Campana,et al.  Localization of Tyrosine Phosphorylated Proteins in Human Sperm and Relation to Capacitation and Zona Pellucida Binding1 , 2003, Biology of reproduction.

[49]  Jindawan Siruntawineti,et al.  Role of acrosomal matrix proteases in sperm-zona pellucida interactions. , 2002, Human reproduction update.

[50]  S. Suarez Formation of a reservoir of sperm in the oviduct. , 2002, Reproduction in domestic animals = Zuchthygiene.

[51]  D. Clapham,et al.  A sperm ion channel required for sperm motility and male fertility , 2001, Nature.

[52]  D. Sakkas,et al.  Protein Tyrosine Phosphorylation in Sperm During Gamete Interaction in the Mouse: The Influence of Glucose1 , 2001, Biology of reproduction.

[53]  B. Gadella,et al.  Dynamics of the mammalian sperm plasma membrane in the process of fertilization. , 2000, Biochimica et biophysica acta.

[54]  G. Kopf,et al.  Cholesterol efflux-mediated signal transduction in mammalian sperm: cholesterol release signals an increase in protein tyrosine phosphorylation during mouse sperm capacitation. , 1999, Developmental biology.

[55]  R. Aitken,et al.  A novel signal transduction cascade in capacitating human spermatozoa characterised by a redox-regulated, cAMP-mediated induction of tyrosine phosphorylation. , 1998, Journal of cell science.

[56]  G. Kopf,et al.  Capacitation of mouse spermatozoa. I. Correlation between the capacitation state and protein tyrosine phosphorylation. , 1995, Development.

[57]  D. Green,et al.  Protein-tyrosine phosphorylation regulates apoptosis in human eosinophils and neutrophils. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[58]  K. Jakobs,et al.  Mechanisms of phospholipase D stimulation by m3 muscarinic acetylcholine receptors. Evidence for involvement of tyrosine phosphorylation. , 1994, European journal of biochemistry.

[59]  K. Bhalla,et al.  Evidence for involvement of tyrosine phosphorylation in taxol-induced apoptosis in a human ovarian tumor cell line. , 1994, Biochemical pharmacology.

[60]  R. Demott,et al.  Hyperactivated sperm progress in the mouse oviduct. , 1992, Biology of reproduction.

[61]  R. Cardullo,et al.  Expression and topographical localization of cell surface fucosyltransferase activity during epididymal sperm maturation in the mouse. , 1989, Gamete research.

[62]  P. Olds-Clarke,et al.  A computer-assisted assay for mouse sperm hyperactivation demonstrates that bicarbonate but not bovine serum albumin is required. , 1987, Gamete research.

[63]  D. Mortimer,et al.  Sperm transport in the human female reproductive tract in relation to semen analysis characteristics and time of ovulation. , 1982, Journal of reproduction and fertility.

[64]  R. Edwards,et al.  REIMPLANTATION OF A HUMAN EMBRYO WITH SUBSEQUENT TUBAL PREGNANCY , 1976, The Lancet.

[65]  L. Nelson,et al.  Fate of surplus sperm in the fallopian tube of the white mouse. , 1975, Biology of reproduction.

[66]  C. R. Austin Observations on the penetration of the sperm in the mammalian egg. , 1951, Australian journal of scientific research. Ser. B: Biological sciences.

[67]  M. C. CHANG,et al.  Fertilizing Capacity of Spermatozoa deposited into the Fallopian Tubes , 1951, Nature.

[68]  Richard R Behringer,et al.  Mouse oviduct development. , 2012, Results and problems in cell differentiation.

[69]  M. Ikawa,et al.  Transgenic mouse sperm that have green acrosome and red mitochondria allow visualization of sperm and their acrosome reaction in vivo. , 2010, Experimental animals.

[70]  S. Suarez Interactions of spermatozoa with the female reproductive tract: inspiration for assisted reproduction. , 2007, Reproduction, fertility, and development.

[71]  E. Berger,et al.  Localization of three human polypeptide GalNAc-transferases in HeLa cells suggests initiation of O-linked glycosylation throughout the Golgi apparatus. , 1998, Journal of cell science.

[72]  O. Hazeki [Phosphoinositide 3-kinase]. , 1997, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

[73]  B. Shur,et al.  Stage-specific increase in cell surface galactosyltransferase activity during spermatogenesis in mice bearing t alleles. , 1988, Developmental biology.