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Published in: Reproductive Medicine and Biology 4/2014

01-10-2014 | Original Article

Time-lapse observations to analyze the effects of assisted hatching

Authors: Maki Goto, Akira Iwase, Naomi Furusawa, Harumi Kobayashi, Nao Kato, Ai Saito, Masahiko Mori, Satoko Osuka, Mika Kondo, Tomoko Nakamura, Tatsuo Nakahara, Hiroyuki Matsumoto, Fumitaka Kikkawa

Published in: Reproductive Medicine and Biology | Issue 4/2014

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Abstract

Purpose

Assisted hatching (AH) is an artificial disruption of the zona pellucida with the aim of facilitating embryo implantation. We used time-lapse observations of mouse embryos to examine the effect of AH in mouse blastocysts.

Methods

AH techniques were performed with acid Tyrode’s solution. We compared the rates of blastocyst formation and blastocyst attachment to Ishikawa cells between the control (n = 28) and the AH group (n = 24). To analyze the effects of AH, 8-cell mice embryos were cultured under time-lapse observations (every 15 min). The time required for hatching, the hatching rates, the frequency of contraction, and the contraction rates in the blastocysts were analyzed.

Results

There were no significant differences between the two groups in hatching rate or attachment rate. The times required for hatching were 286 ± 22 min in the AH group and 990 ± 437 min in the control group (P = 0.018). The contraction frequencies in blastocysts were 3.5 ± 0.7 times in the AH group and 7.5 ± 2.5 times in the control group (P = 0.020).

Conclusions

From the time-lapse observations we found that the time required for hatching and the frequency of contraction in blastocysts were both reduced by AH, although blastocyst formation and attachment were not affected.
Literature
1.
go back to reference Kilani SS, Cooke S, Kan AK, Chapman MG. Do age and extended culture affect the architecture of the zona pellucida of human oocytes and embryos? Zygote. 2006;14(1):39–44.PubMedCrossRef Kilani SS, Cooke S, Kan AK, Chapman MG. Do age and extended culture affect the architecture of the zona pellucida of human oocytes and embryos? Zygote. 2006;14(1):39–44.PubMedCrossRef
2.
go back to reference Ko CS, Ding DC, Chu TW, Chu YN, Chen IC, Chen WH, et al. Changes to the meiotic spindle and zona pellucida of mature mouse oocytes following different cryopreservation methods. Anim Reprod Sci. 2008;105(3–4):272–82.PubMedCrossRef Ko CS, Ding DC, Chu TW, Chu YN, Chen IC, Chen WH, et al. Changes to the meiotic spindle and zona pellucida of mature mouse oocytes following different cryopreservation methods. Anim Reprod Sci. 2008;105(3–4):272–82.PubMedCrossRef
3.
go back to reference Peluso JJ, England-Charlesworth C, Hutz R. Effect of age and of follicular aging on the preovulatory oocyte. Biol Reprod. 1980;22(4):999–1005.PubMedCrossRef Peluso JJ, England-Charlesworth C, Hutz R. Effect of age and of follicular aging on the preovulatory oocyte. Biol Reprod. 1980;22(4):999–1005.PubMedCrossRef
4.
go back to reference Lewis WH, Gregory PW. Cinematographs of living developing rabbit-eggs. Science. 1929;69(1782):226–9.PubMedCrossRef Lewis WH, Gregory PW. Cinematographs of living developing rabbit-eggs. Science. 1929;69(1782):226–9.PubMedCrossRef
5.
go back to reference Gonzales DS, Bavister BD. Zona pellucida escape by hamster blastocysts in vitro is delayed and morphologically different compared with zona escape in vivo. Biol Reprod. 1995;52(2):470–80.PubMedCrossRef Gonzales DS, Bavister BD. Zona pellucida escape by hamster blastocysts in vitro is delayed and morphologically different compared with zona escape in vivo. Biol Reprod. 1995;52(2):470–80.PubMedCrossRef
6.
go back to reference Menezes J, Gunasheela S, Sathananthan H. Video observations on human blastocyst hatching. Reprod Biomed Online. 2003;7(2):217–8.PubMedCrossRef Menezes J, Gunasheela S, Sathananthan H. Video observations on human blastocyst hatching. Reprod Biomed Online. 2003;7(2):217–8.PubMedCrossRef
7.
go back to reference Payne D, Flaherty SP, Barry MF, Matthews CD. Preliminary observations on polar body extrusion and pronuclear formation in human oocytes using time-lapse video cinematography. Hum Reprod. 1997;12(3):532–41.PubMedCrossRef Payne D, Flaherty SP, Barry MF, Matthews CD. Preliminary observations on polar body extrusion and pronuclear formation in human oocytes using time-lapse video cinematography. Hum Reprod. 1997;12(3):532–41.PubMedCrossRef
8.
go back to reference Sathananthan H, Menezes J, Gunasheela S. Mechanics of human blastocyst hatching in vitro. Reprod Biomed Online. 2003;7(2):228–34.PubMedCrossRef Sathananthan H, Menezes J, Gunasheela S. Mechanics of human blastocyst hatching in vitro. Reprod Biomed Online. 2003;7(2):228–34.PubMedCrossRef
9.
go back to reference Massip A, Mulnard J, Vanderzwalmen P, Hanzen C, Ectors F. The behaviour of cow blastocyst in vitro: cinematographic and morphometric analysis. J Anat. 1982;134(Pt 2):399–405.PubMedPubMedCentral Massip A, Mulnard J, Vanderzwalmen P, Hanzen C, Ectors F. The behaviour of cow blastocyst in vitro: cinematographic and morphometric analysis. J Anat. 1982;134(Pt 2):399–405.PubMedPubMedCentral
10.
go back to reference Depypere HT, McLaughlin KJ, Seamark RF, Warnes GM, Matthews CD. Comparison of zona cutting and zona drilling as techniques for assisted fertilization in the mouse. J Reprod Fertil. 1988;84(1):205–11.PubMedCrossRef Depypere HT, McLaughlin KJ, Seamark RF, Warnes GM, Matthews CD. Comparison of zona cutting and zona drilling as techniques for assisted fertilization in the mouse. J Reprod Fertil. 1988;84(1):205–11.PubMedCrossRef
11.
go back to reference Jelinkova L, Pavelkova J, Strehler E, Paulus W, Zivny J, Sterzik K. Improved implantation rate after chemical removal of the zona pellucida. Fertil Steril. 2003;79(6):1299–303.PubMedCrossRef Jelinkova L, Pavelkova J, Strehler E, Paulus W, Zivny J, Sterzik K. Improved implantation rate after chemical removal of the zona pellucida. Fertil Steril. 2003;79(6):1299–303.PubMedCrossRef
12.
go back to reference Mantoudis E, Podsiadly BT, Gorgy A, Venkat G, Craft IL. A comparison between quarter, partial and total laser assisted hatching in selected infertility patients. Hum Reprod. 2001;16(10):2182–6.PubMedCrossRef Mantoudis E, Podsiadly BT, Gorgy A, Venkat G, Craft IL. A comparison between quarter, partial and total laser assisted hatching in selected infertility patients. Hum Reprod. 2001;16(10):2182–6.PubMedCrossRef
13.
go back to reference Petersen CG, Mauri AL, Baruffi RL, Oliveira JB, Massaro FC, Elder K, et al. Implantation failures: success of assisted hatching with quarter-laser zona thinning. Reprod Biomed Online. 2005;10(2):224–9.PubMedCrossRef Petersen CG, Mauri AL, Baruffi RL, Oliveira JB, Massaro FC, Elder K, et al. Implantation failures: success of assisted hatching with quarter-laser zona thinning. Reprod Biomed Online. 2005;10(2):224–9.PubMedCrossRef
14.
go back to reference Ge HS, Zhou W, Zhang W, Lin JJ. Impact of assisted hatching on fresh and frozen-thawed embryo transfer cycles: a prospective, randomized study. Reprod Biomed Online. 2008;16(4):589–96.PubMedCrossRef Ge HS, Zhou W, Zhang W, Lin JJ. Impact of assisted hatching on fresh and frozen-thawed embryo transfer cycles: a prospective, randomized study. Reprod Biomed Online. 2008;16(4):589–96.PubMedCrossRef
15.
go back to reference Kutlu P, Atvar O, Vanlioglu OF. Laser assisted zona thinning technique has no beneficial effect on the ART outcomes of two different maternal age groups. J Assist Reprod Genet. 2010;27(8):457–61.PubMedCrossRefPubMedCentral Kutlu P, Atvar O, Vanlioglu OF. Laser assisted zona thinning technique has no beneficial effect on the ART outcomes of two different maternal age groups. J Assist Reprod Genet. 2010;27(8):457–61.PubMedCrossRefPubMedCentral
16.
go back to reference Sagoskin AW, Levy MJ, Tucker MJ, Richter KS, Widra EA. Laser assisted hatching in good prognosis patients undergoing in vitro fertilization-embryo transfer: a randomized controlled trial. Fertil Steril. 2007;87(2):283–7.PubMedCrossRef Sagoskin AW, Levy MJ, Tucker MJ, Richter KS, Widra EA. Laser assisted hatching in good prognosis patients undergoing in vitro fertilization-embryo transfer: a randomized controlled trial. Fertil Steril. 2007;87(2):283–7.PubMedCrossRef
17.
go back to reference Lemmen JG, Agerholm I, Ziebe S. Kinetic markers of human embryo quality using time-lapse recordings of IVF/ICSI-fertilized oocytes. Reprod Biomed Online. 2008;17(3):385–91.PubMedCrossRef Lemmen JG, Agerholm I, Ziebe S. Kinetic markers of human embryo quality using time-lapse recordings of IVF/ICSI-fertilized oocytes. Reprod Biomed Online. 2008;17(3):385–91.PubMedCrossRef
18.
go back to reference Mio Y, Maeda K. Time-lapse cinematography of dynamic changes occurring during in vitro development of human embryos. Am J Obstet Gynecol. 2008;199(6):660 e661–665 e661.CrossRef Mio Y, Maeda K. Time-lapse cinematography of dynamic changes occurring during in vitro development of human embryos. Am J Obstet Gynecol. 2008;199(6):660 e661–665 e661.CrossRef
19.
go back to reference Wong CC, Loewke KE, Bossert NL, Behr B, De Jonge CJ, Baer TM, et al. Non-invasive imaging of human embryos before embryonic genome activation predicts development to the blastocyst stage. Nat Biotechnol. 2010;28(10):1115–21.PubMedCrossRef Wong CC, Loewke KE, Bossert NL, Behr B, De Jonge CJ, Baer TM, et al. Non-invasive imaging of human embryos before embryonic genome activation predicts development to the blastocyst stage. Nat Biotechnol. 2010;28(10):1115–21.PubMedCrossRef
20.
go back to reference Nishida M, Kasahara K, Kaneko M, Iwasaki H, Hayashi K. Establishment of a new human endometrial adenocarcinoma cell line, Ishikawa cells, containing estrogen and progesterone receptors. Nihon Sanka Fujinka Gakkai Zasshi. 1985;37(7):1103–11.PubMed Nishida M, Kasahara K, Kaneko M, Iwasaki H, Hayashi K. Establishment of a new human endometrial adenocarcinoma cell line, Ishikawa cells, containing estrogen and progesterone receptors. Nihon Sanka Fujinka Gakkai Zasshi. 1985;37(7):1103–11.PubMed
21.
go back to reference Nakahara T, Iwase A, Goto M, Harata T, Suzuki M, Ienaga M, et al. Evaluation of the safety of time-lapse observations for human embryos. J Assist Reprod Genet. 2010;27(2–3):93–6.PubMedCrossRefPubMedCentral Nakahara T, Iwase A, Goto M, Harata T, Suzuki M, Ienaga M, et al. Evaluation of the safety of time-lapse observations for human embryos. J Assist Reprod Genet. 2010;27(2–3):93–6.PubMedCrossRefPubMedCentral
22.
go back to reference Herrero J, Tejera A, Albert C, Vidal C, de los Santos MJ, Meseguer M (2013) A time to look back: analysis of morphokinetic characteristics of human embryo development. Fertil Steril 100(6):1602–1609, e1601–1604. Herrero J, Tejera A, Albert C, Vidal C, de los Santos MJ, Meseguer M (2013) A time to look back: analysis of morphokinetic characteristics of human embryo development. Fertil Steril 100(6):1602–1609, e1601–1604.
23.
go back to reference Kirkegaard K, Kesmodel US, Hindkjaer JJ, Ingerslev HJ. Time-lapse parameters as predictors of blastocyst development and pregnancy outcome in embryos from good prognosis patients: a prospective cohort study. Hum Reprod. 2013;28(10):2643–51.PubMedCrossRef Kirkegaard K, Kesmodel US, Hindkjaer JJ, Ingerslev HJ. Time-lapse parameters as predictors of blastocyst development and pregnancy outcome in embryos from good prognosis patients: a prospective cohort study. Hum Reprod. 2013;28(10):2643–51.PubMedCrossRef
24.
go back to reference Meseguer M, Herrero J, Tejera A, Hilligsoe KM, Ramsing NB, Remohi J. The use of morphokinetics as a predictor of embryo implantation. Hum Reprod. 2011;26(10):2658–71.PubMedCrossRef Meseguer M, Herrero J, Tejera A, Hilligsoe KM, Ramsing NB, Remohi J. The use of morphokinetics as a predictor of embryo implantation. Hum Reprod. 2011;26(10):2658–71.PubMedCrossRef
25.
go back to reference Niimura S, Ogata T, Okimura A, Sato T, Uchiyama Y, Seta T, et al. Time-lapse videomicrographic observations of blastocyst hatching in cattle. J Reprod Dev. 2010;56(6):649–54.PubMedCrossRef Niimura S, Ogata T, Okimura A, Sato T, Uchiyama Y, Seta T, et al. Time-lapse videomicrographic observations of blastocyst hatching in cattle. J Reprod Dev. 2010;56(6):649–54.PubMedCrossRef
26.
go back to reference Cole RJ. Cinemicrographic observations on the trophoblast and zona pellucida of the mouse blastocyst. J Embryol Exp Morphol. 1967;17(3):481–90.PubMed Cole RJ. Cinemicrographic observations on the trophoblast and zona pellucida of the mouse blastocyst. J Embryol Exp Morphol. 1967;17(3):481–90.PubMed
27.
go back to reference Ugajin T, Terada Y, Hasegawa H, Velayo CL, Nabeshima H, Yaegashi N. Aberrant behavior of mouse embryo development after blastomere biopsy as observed through time-lapse cinematography. Fertil Steril. 2010;93(8):2723–8.PubMedCrossRef Ugajin T, Terada Y, Hasegawa H, Velayo CL, Nabeshima H, Yaegashi N. Aberrant behavior of mouse embryo development after blastomere biopsy as observed through time-lapse cinematography. Fertil Steril. 2010;93(8):2723–8.PubMedCrossRef
28.
go back to reference Niimura S. Time-lapse videomicrographic analyses of contractions in mouse blastocysts. J Reprod Dev. 2003;49(6):413–23.PubMedCrossRef Niimura S. Time-lapse videomicrographic analyses of contractions in mouse blastocysts. J Reprod Dev. 2003;49(6):413–23.PubMedCrossRef
Metadata
Title
Time-lapse observations to analyze the effects of assisted hatching
Authors
Maki Goto
Akira Iwase
Naomi Furusawa
Harumi Kobayashi
Nao Kato
Ai Saito
Masahiko Mori
Satoko Osuka
Mika Kondo
Tomoko Nakamura
Tatsuo Nakahara
Hiroyuki Matsumoto
Fumitaka Kikkawa
Publication date
01-10-2014
Publisher
Springer Japan
Published in
Reproductive Medicine and Biology / Issue 4/2014
Print ISSN: 1445-5781
Electronic ISSN: 1447-0578
DOI
https://doi.org/10.1007/s12522-014-0182-4

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