A 40 years journey with fish spermatozoa as companions as I personally experienced it
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu historické články, časopisecké články, přehledy
PubMed
33083947
DOI
10.1007/s10695-020-00882-w
PII: 10.1007/s10695-020-00882-w
Knihovny.cz E-zdroje
- Klíčová slova
- CASA, Flagellum, High-speed video microscopy, Signaling, Sperm guidance,
- MeSH
- AMP cyklický fyziologie MeSH
- dějiny 17. století MeSH
- dějiny 20. století MeSH
- dějiny 21. století MeSH
- draslík fyziologie MeSH
- fertilizace MeSH
- hydrodynamika MeSH
- motilita spermií MeSH
- ryby fyziologie MeSH
- spermie fyziologie MeSH
- teplota MeSH
- vývojová biologie dějiny MeSH
- zvířata MeSH
- Check Tag
- dějiny 17. století MeSH
- dějiny 20. století MeSH
- dějiny 21. století MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- historické články MeSH
- přehledy MeSH
- Názvy látek
- AMP cyklický MeSH
- draslík MeSH
When, in the 1980s, I became interested in the spermatology of fish under the light microscope, active spermatozoa were only visible thanks to their head presenting a sort of "tremor." This situation was quite frustrating given the lack of possible information regarding the motor part called flagellum. We decided to apply simple technologies, including photography. Due to the high speed of the moving fish flagellum, the microscope illumination used a pulsed light strobe combined with a dark field microscope to record the flagellum image despite its small diameter (< 0.5 μm). Then came high-speed cinematographic microscopy up to 200 fps, as well as video cameras. At the end of the 1990s, an automatic moving object video tracking system began to be commercialized (CASA) with main advantages such as (a) a large number of cells tracked, which greatly improves statistics, (b) computer assistance allowing an automatic analysis that provides many motility parameters. Nevertheless, CASA systems are still unable to provide information about fish sperm flagella that move fast. During the 1990s, analog video camera technologies allowed acquisition of flagellum images with high resolution for detailed analysis. Since the 2000s, the use of high-speed video cameras allows the acquisition of images at a much higher resolution and frequency, up to 10,000 frames per second. Since it became possible to visualize the flagella in motion, a noble function was added to that of a propeller: that of a rudder with what a spermatozoon responds to specific signals delivered by the egg for its guidance. In the future, one can wish that an automatic flagella movement analyzer will become functional. This brief anthology puts forward the large amount of progress accomplished during past 40-year period about spermatozoa movement analysis, especially in fish.
Zobrazit více v PubMed
Alavi SMH, Cosson J (2005) Sperm motility in fishes: (II) Effects of ions and osmotic pressure: a review. Cell Biol Int 30:1–14 DOI
Alavi SMH, Cosson J, Bondarenko O, Linhart O (2019) Sperm motility in fishes: (III) diversity of regulatory signals from membrane to the axoneme. Theriogenology 136:143–165 DOI
Allen RD (1985) New observations on cell architecture and dynamics by video-enhanced contrast optical microscopy. Annu Rev Biophys Biophys Chem 14:265–290. https://doi.org/10.1146/annurev.bb.14.060185.001405 PubMed DOI
Baba SA, Mogami Y (1985) An approach to digital image analysis of bending shapes of eukaryotic flagella and cilia. Cell Mot 5:475–489 DOI
Billard R, Cosson J, Crim M, Suquet M (1994) Physiology and quality of sperm in fish. Europ Aquat Soc (Spec Publ) 19:203–218
Billard R, Cosson J, Crim LW, Suquet M (1995) Sperm physiology and quality. In: Bromage NR, Roberts RJ (eds) Broodstock Management and Egg and Larval Quality. Blackwell Sciences, Ltd., Cambridge, pp 25–52
Billard R, Cosson J, Noveiri SB, Pourkazemi M (2004) Cryopreservation and short-term storage of sturgeon sperm, a review. Aquaculture 236(1-4):1–9 DOI
Bondarenko O, Yoshida M, Yoshida M, Ono C, Dzyuba B, Cosson J (2015) The role of Ca
Bondarenko V, Prokopchuk G & Cosson J (2018) Fish sperm flagella: original features and biological implications through the lens of modern technologies. e-book chapter in “Flagella and Cilia: Types, Structure and Functions”. R. Uzbekov Ed., Nova publisher, pp. 49-82
Boryshpolets S, Kholodnyy V, Cosson J, Dzyuba B (2018) Fish sperm motility analysis: the central role of the flagellum. Reprod Fertil Dev 30:833–841. https://doi.org/10.1071/RD17478 PubMed DOI
Brokaw CJ (1984) Automated methods for estimation of sperm flagellar bending parameters. Cell Mot 4:417–430 DOI
Brokaw CJ (1989) Direct measurements of sliding between outer doublet microtubules in swimming sperm flagella. Science 243(4898):1593–1596.a. https://doi.org/10.1126/science.2928796 PubMed DOI
Brokaw CJ (2006) Flagellar propulsion. J Exp Biol 209:985–986 DOI
Butts IAE, Prokopchuk G, Kašpar V, Jacky Cosson J, Pitcher TE (2017) Ovarian fluid impacts flagella beating and biomechanical metrics of sperm between alternative reproductive tactics. J Exp Biol 220:2210–2217. https://doi.org/10.1242/jeb.154195 PubMed DOI
Chauvaud L, Cosson J, Suquet M, Billard R (1995) Sperm motility in turbot (Scophthalmus maximus): initiation of movement and changes with time of swimming characteristics. Environ Biol Fish 43:341–349 (30) DOI
Cosson J (1977) The mitochondrial ATPase complex: structure and function in oligomycin-resistant yeast mutants Saccharomyces cerevisiae. Thèse de Doctorat d'Etat, Université de Paris-Sud (Orsay) N° 1770, defended on April 25 1977
Cosson M-P (1990) Sperm chemotaxis. In: Gagnon C (ed) Controls of Sperm motility: biological and clinical aspects. CRC Press, Boca Raton, pp 103–136
Cosson J (1996) A moving image of flagella: news and views on the mechanisms involved in axonemal beating. Cell Biol Int 20:83–94 DOI
Cosson J (2004) The ionic and osmotic factors controlling motility of fish spermatozoa. Aquac Int 12:69–85 DOI
Cosson J (2008) The motility apparatus of fish spermatozoa. In “Fish Spermatology” (Chapter 9) Alavi SMH, Cosson JJ, Coward K and Rafiee G Eds, Oxford, Alpha Science International Ltd. (ISBN 978-1-84265-369-2), pp 281-316
Cosson J (2012) ATP, the sperm movement energizer. Chapter 1 in “Adenosine Triphosphate: Chemical properties, Biosynthesis and Functions in cells”. Kuestler E. and Traugott G. Editors, Nova Publisher Inc. pp. 1-46. ISBN 978-1-62417-890-0
Cosson J (2015) Flagellar mechanics and sperm guidance. Cosson J. Editor, Bentham Books Publisher. 424 pages, eISBN: 978-1-68-108-128-1, ISBN: 978-1-68-108-129-8. (e-Book 2015)
Cosson J (2019) Fish sperm physiology: structure, factors regulating motility and motility evaluation. In “Recent Developments in Fish Biology Researches”, Yusuf Bozkurt Ed., IntechOpen Publisher (accepted) ISBN 978-1-78923-814-3
Cosson J and Bondarenko V (2019) Structure and beating behavior of the sperm motility apparatus of aquatic animals. Special issue in Theriogenology (accepted). https://doi.org/10.1016/j.theriogenology.2019.06.005
Cosson J and Prokopchuk G (2014) Wave propagation in flagella. In “Wave propagation”; Mateus Gomez Editor, Academy Publish Org. (Cheyenne). pp. 541-583. ISBN: 978-1-941249-01-7
Cosson J, Huitorel P, Gagnon C (2003) How spermatozoa come to be confined to surfaces. Cell Motil Cytoskeleton 54(1):56–63 DOI
Dadras H, Dzyuba B, Cosson J, Golpour A, Siddique MAM, Linhart O (2017) Effect of water temperature on the physiology of fish spermatozoon function: a brief review. Aquac Res 48:729–740 DOI
Darszon A, Beltrán C, Felix R, Nishigaki T, Treviño CL (2001) Ion transport in sperm signaling. Dev Biol 240(1):1–14. https://doi.org/10.1006/dbio.2001.0387 PubMed DOI
Dreanno C, Suquet M, Quemener L, Cosson J, Fierville F, Normand Y, Billard R (1997) Cryopreservation of Turbot (Scophthalmus maximus) sperm. Theriogenology 48:589–603 DOI
Dzyuba V, Cosson J (2014) Motility of fish spermatozoa: from external signaling to flagella response. Reprod Biol 14(3):165–175. https://doi.org/10.1016/j.repbio.2013.12.005 PubMed DOI
Dzyuba B, Bondarenko O, Gazo I, Prokopchuk G, Fedorov P, Cosson J (2017) Energetics of fish spermatozoa: the proven and the possible. Aquaculture 472:60–72. https://doi.org/10.1016/j.aquaculture.2016.05.038 DOI
Dzyuba B, Legendre M, Baroiller JF, Cosson J (2019) Sperm motility of the Nile tilapia (Oreochromis niloticus): effects of temperature on the swimming characteristics. Anim Reprod, accepted. https://doi.org/10.1016/j.anireprosci.2019.01.010
Eisenbach M, Giojalas LC (2006) Sperm guidance in mammals - an unpaved road to the egg. Nat Rev Mol Cell Biol 7(4):276–285. https://doi.org/10.1038/nrm1893 PubMed DOI
Fauvel C, Suquet M, Cosson J (2010) Evaluation and determinism of fish sperm quality. J Appl Ichthyol 26:636–643 DOI
Fawcett DW, Phillips DM (1970) Recent observations on the ultrastructure and development of the mammalian spermatozoon. In: Baccetti B (ed) Spermatologia comparata. Accademia Nazionale Dei Lincei, Roma, pp 13–35
Gagnon C (1995) Regulation of sperm motility at the axonemal level. Reprod Fertil Dev 7:189–198 DOI
Gagnon C (1998) “The Male Gamete: from Basic Knowledge to Clinical Applications” C. Gagnon Ed., Cache River Press (Proceedings of the 8th Int. Symp. on Spermatology, Montréal, August 17-22/1998)
Gallagher MT et al (2019) Rapid sperm capture: high-throughput flagellar waveform analysis. Hum Reprod 34:1173–1185. https://doi.org/10.1093/humrep/dez056 PubMed DOI PMC
Gibbons I (1981) Cilia and flagella of eukaryotes. J Cell Biol:107s–124s. https://doi.org/10.1083/jcb.91.3.107s
Gibbons BH, Gibbons IR (1972) Flagellar movement and adenosine triphosphatase activity in sea urchin sperm extracted with triton X-100. J Cell Biol 54(1):75–97. https://doi.org/10.1083/jcb.54.1.75 PubMed DOI PMC
Gillies EA, Bondarenko V, Cosson J, Pacey AA (2013) Fins improve the swimming performance of fish sperm: a hydrodynamic analysis of the Siberian sturgeon Acipenser baerii. Cytoskeleton 70(2):85–100. https://doi.org/10.1002/cm.21093 PubMed DOI
Gray J, Hancock GJ (1955) The propulsion of sea-urchin spermatozoa. J Exp Biol 32:802–814 DOI
Holwill ME (1966) Physical aspects of flagellar movement. Physiol Rev 46:696–785 DOI
Holwill ME, Satir P, Sugrue PA, Avolio J (1991) Modelling the axoneme. In: Baccetti B (ed) Comparative Spermatology 20 years after. Raven Press, Rome, pp 377–384
Huitorel P, Audebert S, White D, Cosson J and Gagnon C (1999) Role of tubulin epitopes in the regulation of flagellar motility Book chapter in “The Male Gamete: from Basic Knowledge to Clinical Applications” C. Gagnon Ed., Cache River Press (Proceedings of the 8th Int. Symp. on Spermatology, Montréal, Canada, August 17-22/1998) pp.475-492
Inaba K, Dreanno C, Cosson J (2003) Control of flatfish sperm motility by CO2 and carbonic anhydrase. Cell Motil Cytoskeleton 55:174–187 DOI
Ishimoto K, Cosson J, Gaffney EA (2016) A simulation study of sperm motility hydrodynamics near fish eggs and spheres. J Theor Biol 389:187–197. https://doi.org/10.1016/j.jtbi.2015.10.013 PubMed DOI
Linhart O, Cosson J, Rodina M (2000) Rodina. Cryopreservation of sperm in common carp, Cyprinus carpio: sperm motility and embryonic hatching success. Cryobiology 41:241–250 DOI
Linhart O, Hadi ASM, Marek R, David G, Cosson J (2008a) After finishing of motility, common carp (Cyprinus carpio) sperm is able to re-initiate a second motility period and to fertilize eggs. Cybium 32(2):187–188
Linhart O, Alavi SMH, Rodina M, Gela D, Cosson J (2008b) Comparison of sperm velocity, motility rate and fertlilizing ability of firstly and secondly activated carp sperm. J Appl Ichthyol 24:386–392 DOI
Miller RL (1973) Chemotaxis of animal spermatozoa. In: Perez Miravete A (ed) Behavior of microorganisms. Plenum Press, London, pp 31–47
Miller RL (1985) Sperm chemo-orientation in metazoa. In: Metz CB, Monroy A (eds) Biology of fertilization, vol 2. Academic Press, New York, pp 275–337. https://doi.org/10.1016/B978-0-12-492602-8.50015-2 DOI
Morisawa M (1994) Cell signaling mechanisms for sperm motility. Zool Sci 11(5):647–662
Morisawa M, Ishida K (1987) Short-term changes in levels of cyclic AMP, adenylate cyclase, and phosphodiesterase during the initiation of sperm motility in rainbow trout. J Exp Zool 242(2):199–204 DOI
Pacey A, Cosson J, Bentley M (1994) The acquisition of forward motility in the sperm of the polychaete Arenicola marina (L.). J Exp Biol 195(1):259–280.a DOI
Perchec G, Jeulin C, Cosson J, Andre F, Billard R (1995) Relationship between sperm ATP content and motility of carp spermatozoa. J Cell Sci 108:747–753 (58) DOI
Perchec-Poupard G, Gatti J-L, Cosson J, Jeulin C, Fierville F, Billard R (1997) Effects of extracellular environment on the osmotic signal transduction involved in activation of motility of carp spermatozoa. J Reprod Fertil 110(2):315–327. https://doi.org/10.1530/jrf.0.1100315 PubMed DOI
Prokopchuk G and Cosson J (2017) Biophysics of fish sperm flagellar movement: up-dated knowledge and original directions. Book chapter in “Cytoskeleton. - Structure, Dynamics, Function and Disease” Jose C. Jimenez-Lopez Ed., Intech open access Publisher, pp. 127-150. ISBN 978-953-51-3170-0
Prokopchuk G, Dzuba B, Boryshpolet S, Linhart O, Cosson J (2015) Motility initiation in fish spermatozoa: description of the propagation of very first initial waves. Theriogenology 84(1):51–61. https://doi.org/10.1016/j.theriogenology.2015.02.011 PubMed DOI
Prokopchuk G, Dzyuba B, Rodina M, Cosson J (2016) Control of sturgeon sperm motility: antagonism between K+ ions concentration and osmolarity. Anim Reprod 164:82–89. https://doi.org/10.1016/j.anireprosci.2015.11.015 DOI
Sato H, Greuet C, Cachon M, Cosson J (2004) Analysis of the contraction of an organelle using its birefringency: the R-fibre of the Ceratium (Dinoflagellate) flagellum. Cell Biol Int 28-5:387–396 DOI
Saudrais C, Fierville F, Cibert C, Loir M, Le Rumeur E, Cosson J (1998) The use of phosphocreatine plus ADP as energy source for motility of membrane deprived trout spermatozoa. Cell Motil Cytoskeleton 41:91–106 DOI
Schöevaërt D et al (1990) A new automated method of image analysis: comparison of ciliary and flagellar beats. Biorheology 27:567–579 DOI
Shaliutina-Kolešová A, Gazo I, Cosson J, Linhart O (2014) Protection of common carp (Cyprinus carpio L.) spermatozoa motility under oxidative stress by antioxidants and seminal plasma A. Fish Physiol Biochem 40(6):1771–1781. https://doi.org/10.1007/s10695-014-9966-z PubMed DOI
Suquet M, Dreanno C, Fauvel C, Cosson J, Billard R (2000) Cryopreservation of sperm in marine fish. Aquac Res 31:231–243 DOI
Tsvetkova LI, Cosson J, Linhart O, Billard R (1996) Motility & fertilizing capacity of fresh & frozen-thawed spermatozoa in sturgeons (Acipenser baeri & A. ruthenus). J Appl Ichthyol 12:107–112 DOI
van Leeuwenhoek A (1678) Observationes de natis e semine genitali animalculis. Phil Trans R Soc A 12:1040–1046
Yanagimachi R, Cherr G, Matsubara T, Andoh T, Harumi T, Vines C, Pillai M, Griffin F, Matsubara H, Weatherby T, Kaneshiro K (2013) Sperm attractant in the micropyle region of fish and insect eggs. Biol Reprod 88(2):47. https://doi.org/10.1095/biolreprod.112.105072 PubMed DOI
Yoshida M, Murata M, Inaba K, Morisawa M (2002) A chemoattractant for ascidian spermatozoa is a sulfated steroid. Proc Natl Acad Sci U S A 99(23):14831–14836 DOI
Yoshida M, Ishikawa M, Izumi H, De Santis R, Morisawa M (2003) Store-operated calcium channel regulates the chemotactic behavior of ascidian sperm. Proc Natl Acad Sci U S A 100(1):149–154 DOI