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84. Ikenaga, J. and Yoshida, M.
Sperm activation and chemotaxis of invertebrates.
in “Reproduction in Aquatic Animals: From Basic Biology to Aquaculture Technology” (Eds. Yoshida, M. and Asturiano J.), Springer-Nature, (2020) in press.
83. Yoshida, M.
Overview: Reproductive systems in aquatic animals.
in “Reproduction in Aquatic Animals: From Basic Biology to Aquaculture Technology” (Eds. Yoshida, M. and Asturiano J.), Springer-Nature, (2020) in press.
82. Yoshida, M. and Astriano J. eds.
Reproduction in Aquatic Animals: From Basic Biology to Aquaculture Technology
Springer-Nature, (2020) in press.
81. Shindo, M., Inui, M., Kang, W., Tamano, M., Tingwei, C., Takada, S., Hibino, T., Yoshida, M., Yoshida, K., Okada, H., Iwamoto, T., Miyado, K., and Kawano, N.
Deletion of a seminal gene cluster reinforces a crucial role of SVS2
in male fertility.
International Journal of Molecular Sciences, 20(18): 4557 (2019). doi:10.3390/ijms20184557
80. Ikenaga, J., Hookabe, N., Kohtsuka, H., Yoshida, M., and Kajihara, H.
A Population Without Female: Males of Baseodiscus delineatus (Nemertea: Heteronemertea) Reproduce Asexually by Fragmentation.
Zoological Science, 36(4): 348-353(2019) doi: 10.2108/zs180203
79. Kinoshita-Terauchi，N., Shiba, K., Terauchi, M., Romero, F., Ramírez-Gómez, H. V., Yoshida, M., Motomura, T., Kawai, H. and Nishigaki, T.
High potassium seawater inhibits ascidian sperm chemotaxis, but does not affect the male gamete chemotaxis of a brown alga.
Zygote, Jul 18:1-7. (2019). doi: 10.1017/S0967199419000224
78. 吉田 薫，吉田 学
受精時に見られる精子運動調節
細胞 51（5）：253-255（2019）
77. 吉田 学、佐藤賢一、原山 洋
第5章 受精〜個体発生のはじまり
発生生物学〜基礎から応用展開〜（塩尻信義・弥益恭・加藤容子・加野浩一郎・中尾啓子 編）
培風館（2019）pp.38-46 ISBN 978-4-563-7823-2
76. Yoshida, K., Shiba, K., Sakamoto, A., Ikenaga, J., Matsunaga, S., Inaba, K., and Yoshida, M.
Ca2+ efflux via plasma membrane Ca2+-ATPase mediates chemotaxis in ascidian sperm.
Scientific Reports 8: 16622 (2018). DOI:10.1038/s41598-018-35013-2
75. Watanabe, T., Shibata, H., Ebine, M., Tsuchikawa, H., Matsumori, N., Murata, M., Yoshida, M., Morisawa, M., Lin, S., Yamauchi, K., Sakai, K., and Oishi, T.
Synthesis and Complete Structure Determination of Sperm Activating and Attracting Factor Isolated from the Ascidian Ascidia sydneiensis.
Journal of Natural Products 81(4): 985-997 (2018). DOI: 10.1021/acs.jnatprod.7b01052
74. Yoshida, M., Kawano, N., Iwamoto, T., and Yoshida, K.
Chapter 61．Seminal vesicle – structure –
in “Encycropedia of Reproduction 2nd. Edition Vol. 1: Male Reproduction” (Eds. by Skinner, M. and Jégou, B.) Elsevier, (2018) pp.344-348. doi: 10.1016/B978-0-12-801238-3.64599-3
73. 吉田 学
第7章 鞭毛繊毛運動
動物学の百科事典 日本動物学会監修 丸善（2018）pp406-407. ISBN:978-4-621-30309-2
72. 吉田 学
第7章 精子運動と精子活性化
魚類学の百科事典 日本動物学会監修 丸善（2018）pp360-361. ISBN:978-4621303177
71. Yoshida, M. and Yoshida, K.
Modulation of sperm motility and function prior to fertilization
in “Reproductive and Developmental Strategies: the Continuity of Life” (Ed. by K. Kobayashi, T. Kitano, Y. Iwao, & M. Kondo) Springer, Tokyo Japan. pp437-462 (2018) DOI:10.1007/978-4-431-56609-0_21 ISBN: 978-4431566076
70. Arima，H., Tsutsui, H., Sakamoto, A., Yoshida, M., and Okamura, Y.
Induction of divalent cation permeability by heterologous expression of a voltage sensor domain
Biochimica et Biophysica Acta – Biomembranes 1860: 981-990 (2018). doi: 10.1016/j.bbamem.2018.01.004
69. Yoshida, M., Kurokawa, D., Asturiano, J.F., Fraser, G.
Embryogenic development of the grass pufferfish (Takifugu niphobles): from egg to larvae.
Theriogenology 90: 191-196 (2017). doi: 10.1016/j.theriogenology.2016.12.005
68. Araki, N., Yoshida, K., Kang, W. Kawano, N., Miyado, K., and Yoshida, M.
Seminal vesicle proteins SVS3 and SVS4 facilitate SVS2 effect on sperm capacitation
Reproduction 152: 313-321 (2016). doi:10.1530/REP-15-0551
67. Kang, W. Kawano, N., Yamatoya, K., Yoshida, K., Yoshida, M., and Miyado, K.
Critical roles of seminal plasma on sperm migration in the female reproductive tract.
Journal of Reproduction Engineering 18: 5-10 (2016).
66. Yoshida, M. and Inaba, K.
Sperm Chemotaxis in Urochordates.
in "Flagellar Mechanics and Sperm Guidance" (Ed. by J. Cosson), Bentham Science Publishers, Sharjah, UAE (2015) pp183-207. doi: 10.2174/97816810812811150101
ISBN 978-1-68108-129-8
65. Ono, C., Yoshida, M., Kawano, N., Miyado, K., and Umezawa, A.
Staphylococcus epidermidis is involved in a mechanism for female reproduction in mice.
Regenerative Therapy 1:11–17 (2015). doi:10.1016/j.reth.2014.12.003
64. Miyashiro, D. Shiba, K., Miyashita, T., Baba, S., Yoshida, M., and Kamimura, S.
Chemotactic response with a constant delay-time mechanism in Ciona spermatozoa revealed by a high time resolution analysis of flagellar motility.
Biology Open 4:109-118 (2015). doi: 10.1242/ bio.20137351
63. Araki, N., Trencsenyi, G., Krasznai, Z. T., Nizsaloczki, E., Sakamoto, A., Kawano, N., Miyado, K., Yoshida, K., and Yoshida, M.
Seminal vesicle secretion 2 acts as a protectant of sperm sterols and prevents ectopic sperm capacitation in mice.
Biology of Reproduction 92 (1): 8, 1-10 (2015). doi:10.1095/biolreprod.114.120642
62. Nonaka, M.I., Zsigmond, E., Kudo, A., Kawakami, H., Yoshida, K., Yoshida, M., Kawano, N., Miyado, K., Nonaka, M., Wetsel, R.A.
Epididymal C4b-binding protein is processed and degraded during transit through the duct and is not essential for fertility.
Immunobiology 220:467-475 (2015). doi:10.1016/j.imbio.2014.11.001
61. Hiradate Y., Inoue, H., Kobayashi, N., Shirakata, Y., Suzuki, Y., Goto A., Roh, S., Uchida, T., Katoh, K., Yoshida, M., Sato, E., and Tanemura, K.
Neurotensin enhances sperm capacitation and the acrosome reaction.
Biology of Reproduction 91 (2): 53, 1-9 (2014). doi:10.1095/biolreprod.113.112789
60. Gallego, V., Pérez, L., Asturiano, J. F., and Yoshida, M.
Sperm motility parameters and spermatozoa morphometric characterization in marine species: a study of swimmer and sessile species.
Theriogenology 82 (5): 668-676 (2014). doi: 10.1016/j.theriogenology.2014.05.026.
59. 稲葉一男、柴 小菊、吉田 学
第17章 精子運動の活性化と走化性
動植物の受精学 (澤田 均 編)
化学同人（2014） pp286-300. ISBN: 978-4-759815-12-2
58. Kawano, N., Araki, N., Yoshida, K., Hibino, T., Ohnami, N., Makino, M., Kanai S., Hasuwa, H., Yoshida, M., Miyado, K., and Umezawa, A.
Seminal vesicle protein SVS2 is required for sperm survival in the uterus.
Proceedings of the National Academy Sciences USA 111 (11), 4145-4150 (2014) doi: 10.1073/pnas.1320715111
57. Yoshida, M.
Sperm chemotaxis: the first authentication events between conspecific gametes before fertilization.
in "Sexual Reproduction in Animals and Plants."
(Ed. by H. Sawada, N. Inoue, & M. Iwano),
Springer, Tokyo Japan. pp3-11. ISBN 978-4-431-54588-0 (2014).
56. Gallego, V., Perez, L., Asturiano, J. F., and Yoshida, M.
Relationship between spermatozoa motility parameters, sperm/egg ratio, fertilization success and hatching rates in the puffer fish (Takifugu niphobles).
Aquaculture 416–417:238-243 (2013)
55. Gallego, V., Perez, L., Asturiano, J. F., and Yoshida, M.
Study of puffer fish (Takifugu niphobles) sperm: development of methods for short-term storage, effect of different activation role of intracellular changes in Ca2+ and K+ in the initiation motility.
Aquaculture 414-415: 82-91 (2013).
54. Yoshida, M., Hiradate, Y, Sensui, N., Cosson, J., and Morisawa, M.
Species-specificity of sperm motility activation and chemotaxis: a study on ascidian species.
Biological Bulletin, 224 (3)156-165 (2013).
53. Matsumori, N., Hiradate, Y., Shibata, H., Oishi, T., Simma, S., Toyoda, M., Hayashi, F., Yoshida, M, Murata, M, and Morisawa, M.
A Novel Sperm-Activating and Attracting Factor (SAAF) from the Ascidian Ascidia sydneiensis.
Organic Letters, 15 (2), 294-297 (2013).
52. Sensui, N., Yoshida, M. and Tachibana, K.
Role of Mos/MEK/ERK cascade and Cdk1 in Ca2+ oscillations in fertilized ascidian eggs.
Developmental Biology, 367, 208-215 (2012).
51. Yoshida, M.
Regulation of sperm chemotaxis in the ascidian, Ciona intestinalis.
in "Sperm Cell Research in the 21st Century: Historical Discoveries to New Horizons."
(Ed. by M Morisawa),
Adthree Publishing Co., Tokyo, Japan (2012) pp157-162 .
50. Yoshida M., and Yoshida, K.
Sperm chemotaxis and regulation of flagellar movement by Ca2+
Molecular Human Reproduction 17, 457-465 (2011).
49. Kambara, Y., Shiba, K., Yoshida, M., Sato, C., Kitajima, K., and Shingyoji, C.
Mechanism regulating Ca2+-dependent mechanosensory behaviour in sea urchin spermatozoa.
Cell Structure and Function 36, 69-82 (2011).
48. Kawano, N., Yoshida, K., Miyado, K., and Yoshida, M.
Lipid Rafts: Keys to Sperm Maturation, Fertilization, and Early Embryogenesis.
Journal of Lipids (2011), Article ID 264706, 10 pages
47. Yoshida, K., Iwamoto, T. and Yoshida, M.
Effects of the seminal plasma proteins semenogelin (SEMG)/seminal vesicle secretion 2 (SVS2) on sperm fertility.
in “Human Spermatozoa: Maturation, Capacitation and Abnormalities.”
(Eds. by T. Lejeune and P. Delvaux),
Nova Science Publishers, Inc., Hauppauge NY, (2010) pp.205-220.
46. Kawano, N., Ito, J., Kashiwazaki, N., and Yoshida, M.
Phosphorylation of the MAPK pathway has an essential role in the acrosome reaction in miniature pig sperm.
Reproduction in Domestic Animals, 45, 263-268 (2010).
45. Yoshida, K., Krasznai, Z. T., Krasznai, Z., Yoshiike, M., Kawano, N., Yoshida, M., Morisawa, M., Toth, Z., Bazsane, Z. K., Marian, T., and Iwamoto, T.
Functional implications of membrane modification with semenogelins for inhibition of sperm motility in humans.
Cell Motility and the Cytoskeleton, 66, 99-108 (2009).
44. Shiba, K., Baba, S., Inoue, T., and Yoshida, M.
Ca2+ bursts occur around a local minimal concentration of attractant and trigger sperm chemotactic response.
Proceedings of the National Academy Sciences USA, 105, 19311-19316 (2008).
43. Kawano, N., Yoshida, K., Iwamoto, T. and Yoshida, M.
Ganglioside GM1 mediates decapacitation effects of SVS2 on murine spermatozoa.
Biology of Reproduction, 79, 1153-1159 (2008).
42. Yoshida, M., Kawano, N., and Yoshida, K.
Control of Sperm Motility and Fertility: Diverse factors and common mechanisms.
Cellular and Molecular Life Sciences 65, 3446-3457, (2008).
41. Yoshida, M., Yoshida, K., Shiba, K., Tsuchikawa, H., Ootou, O., Oishi, T. and Murata, M.
Ascidian sperm activating and attracting factor: importance of sulfate groups for the activities and implication of its putative receptor.
FEBS letters, 582, 3429-3433 (2008).
40. Kondoh, E., Konno, A., Inaba, K., Oishi, T. Murata, M., and Yoshida, M.
Valosin-containing protein/p97 interacts with sperm-activating and sperm-attracting factor (SAAF) in the ascidian egg and modulates sperm-attracting activity.
Development Growth & Differenciation, 50, 665-673 (2008).
39. Kowalski, R.K., Shiba, K., Yoshida, M. and Glogowski, J.
Prostaglandins in rainbow trout (Oncorhynchus mykiss WALBAUM, 1792) sperm biology − seraching for answers.
Journal of Applied Ichthyology, 24,487-491(2008).
38. Yoshida, K., Kawano, N., Yoshiike, M., Yoshida, M., Iwamoto, T., and Morisawa, M.
Physiological roles of semenogelin and zinc in sperm motility and semen coagulation at ejaculation in human.
Molecular Human Reproduction, 14, 151-156 (2008).
37. Kawano, N. and Yoshida, M.
Seminal vesicle protein, secretion 2 (SVS2) controls mouse sperm fertility.
Biology of Reproduction, 76, 353-361 (2007).
36. 森澤正昭、吉田 学
精子の活性化・走化性機構
新編精子学 毛利秀雄・星元紀 監修 東京大学出版会 (2006) 94-115.
35. Shiba, K., Marian, T., Krasznai, Z., Baba, S., Morisawa, M. and Yoshida, M.
Na+/Ca2+ exchanger modulates the flagellar wave pattern for the regulation of motility activation and chemotaxis in the ascidian spermatozoa.
Cell Motility and the Cytoskeleton, 63, 623-632 (2006).
34. Matsu-ura, T., Michikawa, T., Inoue, T., Miyawaki, A., Yoshida, M., and Mikoshiba, K.
Cytosolic inositol 1,4,5-trisphosphate dynamics during intracellular calcium oscillations in living cells.
Journal of Cell Biology, 173, 755-765 (2006)
33. Murata, M., Oishi, T. and Yoshida, M.
State-of-art Methodology of Marine Natural Products Chemistry: Structure Determination with Extremely Small Sample Amounts.
in "Antifouling Compounds." (Eds. by N Fusetani, AS Clare, & WEG Muller) (Series: Progress in Molecular and Subcellular Biology. Vol.42) , Springer-Verlag, Berlin Heidelberg, (2006) 203-220.
32. 柴 小菊、吉田 学
ユウレイボヤ精子の運動調節機構
号外海洋 41, 98-104 (2005).
31. Morisawa, M. and Yoshida, M.
Activation of Motility and Chemotaxis in the Spermatozoa: from invertebrates to humans
Reproductive Medicine and Biology, 4, 101-114 (2005).
30. Nomura, M., Yoshida, M., and Morisawa, M.
Calmodulin/Calmodulin-dependent protein kinase II mediates SAAF-induced motility activation of ascidian sperm.
Cell Motility and the Cytoskeleton, 59, 28-37 (2004).
29. Oishi, T., Tuchikawa, H., Murata, M., Yoshida, M., and Morisawa, M.
Synthesis and identification of an endogenous sperm activating and attracting factor isolated from ascidian Ciona intestinalis; an example of nanomolar-level structure elucidation of novel natural compound.
Tetrahedron, 60, 6971-6980 (2004).
28. 吉田 学
精子の走化性応答のしくみ
生化学 76, 45-50 (2004).
27. 森沢正昭、吉田 学、東郷 建
受精のしくみを探る新しい研究
遺伝 58, 30-36 (2004).
26. Yoshida M.
Fertilization and sperm chemotaxis in ascidians.
Methods in Molecular Biology, 253, 13-25 (2004).
25.Yoshida M.
Mechanism of Chemotaxis of the Ascidian Spermatozoa.
Zoological Science 20, 1499-1500 (2003).
24. Oishi T., Tuchikawa H., Murata M., Yoshida M., and Morisawa M.
Synthesis of endogenous sperm-activating and attracting factor isolated from ascidian Ciona intestinalis.
Tetrahedron Letters, 44, 6387-6389 (2003)
23. 吉田 学
卵による精子の活性化・誘引機構の研究
生物科学ニュース 380, 23-27 (2003)
22. Yoshida, M., Horiuchi, Y., Sensui, N., and Morisawa, M.
Signaling from [Ca2+]i transients to the ooplasmic segregation through small GTPase rho in the ascidian egg.
Development Growth & Differenciation, 45, 275-281 (2003).
21． Kimura, Y., Yoshida, M., and Morisawa, M.
Interaction between noradrenalin or adrenalin and b1-adrenergic receptor in the nervous system triggers early metamorphosis of the larvae in the ascidian, Ciona savignyi.
Developmental Biology. 258, 129-140 (2003).
20. Fukami, K., Yoshida, M., Inoue, T., Kurokawa, M., Fissore, R., Yoshida, N., Mikoshiba, K., and Takenawa, T.
Phospholipase Cd4 is required for Ca2+-mobilization essential for acrosome reaction in sperm.
Journal of Cell Biology, 161, 79-88 (2003).
19. 村田道雄、大石 徹、吉田 学
生物現象鍵物質の微量構造決定
化学と生物 41, 114-117 (2003).
18. Yoshida, M., Ishikawa, M., Izumi, H., DeSantis, R., and Morisawa, M.
Store operated calcium channel regulates chemotactic behavior of ascidian sperm.
Proceedings of the National Academy Sciences USA, 100, 149-154 (2003)
17. Yoshida, M., Murata, M., Inaba, K, and Morisawa, M.
A chemoattractant for ascidian spermatozoa is a sulfated steroid.
Proceedings of the National Academy of Sciences USA, 99, 14831-14836 (2002).
16. Yoshida, M., Murata M., and Morisawa M.
A sulfated steroid regulates ascidian sperm chemotaxis.
in "Proceedings of 9th International Symposium on Spermatology", Eds. by G. Van Der Horst, D. Franken, R. Bornman, T. De Jager, and S. Dyer, Monduzzi Editore, Bologna (Italy), pp109-112 (2002).
15． Yoshida, M., Horiuchi, Y., and Morisawa, M.
Calcium transients signal ooplasmic segregation through the small GTPase rho in ascidian eggs.,
in "The Biology of Ascidians", Eds. by H. Sawada, H. Yokosawa, and C.C. Lambert, Springer, Tokyo, pp 80-85 (2001).
14． Kimura, Y., Yoshida, M., and Morisawa, M.
Participation of Neurotransmitters and adrenergic receptor with metamorphosis of ascidian larvae.
in "The Biology of Ascidians", Eds. by H. Sawada, H. Yokosawa, and C.C. Lambert, Springer, Tokyo, pp 241-245, (2001).
13． Sensui, N., Yoshida, M., and Morisawa, M.
Roles of PI3 kinase and MLCK on egg deformation and ooplasmic segregation at fertilization in the ascidian, Ciona savignyi.
in "The Biology of Ascidians", Eds. by H. Sawada, H. Yokosawa, and C.C. Lambert, Springer, Tokyo, pp 92-96, (2001).
12． Morisawa, M., Izumi, H., Yoshida, M., and Oka, Y.
Cell signalings for activation of motility and chemotaxis in the sperm of Ciona.
in "The Biology of Ascidians", Eds. by H. Sawada, H. Yokosawa, and C.C. Lambert, Springer, Tokyo, pp 86-91, (2001).
11． Yoshida, M., Horiuchi, Y., and Morisawa, M.
Changes in intracellular calcium controls rho protein-mediated ooplasmic segregation in the ascidian egg. Journal of Reproduction and Development, 46 Suppl: 73-74, (2000).
10． Morisawa, M., Oda, S., Yoshida, M., and Takai, H.
Transmembrane signal transduction for the regulation of sperm motility in fishes and ascidians.
in "Male Gamete: from basic knowledge to clinical applications." Ed. by C. Gagnon, Cache River Press, Vienna, pp 149-160, (1999).
9. Yoshida, M., Sensui, N., Inoue, T., Morisawa, M., and Mikoshiba, K.
Role of two series of Ca2+ oscillations on activation of ascidian eggs.
Developmental Biology, 203, 122-133 (1998).
8． Yoshida, M., Sensui, N., Inoue, T., Morisawa, M., and Mikoshiba, K.
Egg activation and meiosis are controlled by inositol 1,4,5-trisphosphate-induced calcium release in ascidian eggs.
Zygote 6 Suppl: S141-S142, (1998).
7． Yoshida, M. and Mikoshiba, K.
Mechanism and role of two series of Ca2+ oscillations in ascidian eggs.
Journal of Reproduction and Development, 44 Suppl: 32, (1998).
6． Sensui, N., Yoshida, M., and Morisawa, M.
Effect of GTP-g-S and GDP-b-S on the activation of ascidian egg.
Journal of Reproduction and Development, 44 Suppl: 48, (1998).
5． Nomura, M., Yoshida, M., Inaba, K. and Morisawa, M.
Calmodulin (CaM)-mediated sperm acitvation in the ascidian, Ciona intestinalis.
Journal of Reproduction and Development, 44 Suppl: 52, (1998).
4. Yoshida, M., Inaba, K., Ishida, K., and Morisawa, M.
Calcium and Cyclic AMP Mediate Sperm Activation, but Ca2+ Alone Contributes Sperm Chemotaxis in the Ascidian, Ciona savignyi.
Development Growth & Differentiation, 36, 589-595, (1994).
3. Yoshida, M., Inaba, K., and Morisawa, M.
Sperm Chemotaxis during the Process of Fertilization in the Ascidians, Ciona savignyi and Ciona intestinalis.
Developmental Biology , 157, 497-506, (1993).
2． Yoshida, M., Inaba, K., and Morisawa, M.
Activation and chemotactic behavior of ascidian spermatozoa.
Cell Motility and Cytoskeleton 23: 304 (1992).
1. Shiokawa, K., Yoshida, M., Hukamachi, H., Fu, Y., Tashiro, K., and Sameshima, M.
Cytological Studies of Large Nucleus-Like Structures Formed by Exogenously-Injected Linear and Circular DNAs in Fertilized Eggs of Xenopus laevis.
Development Growth & Differentiation 34, 79-90, (1992).
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