
Comparative study of preimplantation development following distinct assisted oocyte activation protocols in a PLC-zeta knockout mouse model
- Author
- Minerva Ferrer Buitrago (UGent) , Laurentijn Tilleman (UGent) , Vanessa Thys (UGent) , A Hachem, Annekatrien Boel (UGent) , Filip Van Nieuwerburgh (UGent) , Dieter Deforce (UGent) , Luc Leybaert (UGent) , Petra De Sutter (UGent) , J. Parrington and Björn Heindryckx (UGent)
- Organization
- Abstract
- Mammalian fertilization encompasses a series of Ca2+ oscillations initiated by the sperm factor phospholipase C zeta (PLC zeta). Some studies have shown that altering the Ca2+ oscillatory regime at fertilization affects preimplantation blastocyst development. However, assisted oocyte activation (AOA) protocols can induce oocyte activation in a manner that diverges profoundly from the physiological Ca2+ profiling. In our study, we used the newly developed PLC-null sperm to investigate the independent effect of AOA on mouse preimplantation embryogenesis. Based on previous findings, we hypothesized that AOA protocols with Ca2+ oscillatory responses might improve blastocyst formation rates and differing Ca2+ profiles might alter blastocyst transcriptomes. A total of 326 MII B6D2F1-oocytes were used to describe Ca2+ profiles and to compare embryonic development and individual blastocyst transcriptomes between four control conditions: C I (in-vivo fertilization), C2 (ICSI control sperm), C3 (parthenogenesis) and C4 (ICSI-PLC zeta-KO sperm) and four AOA groups: AOA1 (human recombinant PLC zeta, AOA2 (Sr2+), AOA3 (ionomycin) and AOA4 (TPEN). All groups revealed remarkable variations in their Ca2+ profiles; however, oocyte activation rates were comparable between the controls (91.1% +/- 13.8%) and AOA (86.9% +/- 11.1%) groups. AOA methods which enable Ca2+ oscillatory responses (AOA1: 41% and AOA2: 75%) or single Ca2+ transients (AOA3: 50%) showed no significantly different blastocyst rates compared to ICSI control group (C2: 70%). In contrast, we observed a significant decrease in compaction (53% vs. 83%) and blastocyst rates (41% vs. 70%) in the absence of an initial Ca2+ trigger (AOA4) compared with the C2 group. Transcription profiles did not identify significant differences in gene expression levels between the ICSI control group (C2) and the four AOA groups.
- Keywords
- assisted oocyte activation, calcium oscillations, blastocyst development, phospholipase C zeta, transcriptomics, animal model, PHOSPHOLIPASE-C-ZETA, EGG-ACTIVATION, CA2+ OSCILLATIONS, PARTHENOGENETIC ACTIVATION, FERTILIZATION FAILURE, CALCIUM OSCILLATIONS, ICSI, SIGNAL, INFERTILITY, INJECTION
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-8697128
- MLA
- Ferrer Buitrago, Minerva, et al. “Comparative Study of Preimplantation Development Following Distinct Assisted Oocyte Activation Protocols in a PLC-Zeta Knockout Mouse Model.” MOLECULAR HUMAN REPRODUCTION, vol. 26, no. 11, 2020, pp. 801–15, doi:10.1093/molehr/gaaa060.
- APA
- Ferrer Buitrago, M., Tilleman, L., Thys, V., Hachem, A., Boel, A., Van Nieuwerburgh, F., … Heindryckx, B. (2020). Comparative study of preimplantation development following distinct assisted oocyte activation protocols in a PLC-zeta knockout mouse model. MOLECULAR HUMAN REPRODUCTION, 26(11), 801–815. https://doi.org/10.1093/molehr/gaaa060
- Chicago author-date
- Ferrer Buitrago, Minerva, Laurentijn Tilleman, Vanessa Thys, A Hachem, Annekatrien Boel, Filip Van Nieuwerburgh, Dieter Deforce, et al. 2020. “Comparative Study of Preimplantation Development Following Distinct Assisted Oocyte Activation Protocols in a PLC-Zeta Knockout Mouse Model.” MOLECULAR HUMAN REPRODUCTION 26 (11): 801–15. https://doi.org/10.1093/molehr/gaaa060.
- Chicago author-date (all authors)
- Ferrer Buitrago, Minerva, Laurentijn Tilleman, Vanessa Thys, A Hachem, Annekatrien Boel, Filip Van Nieuwerburgh, Dieter Deforce, Luc Leybaert, Petra De Sutter, J. Parrington, and Björn Heindryckx. 2020. “Comparative Study of Preimplantation Development Following Distinct Assisted Oocyte Activation Protocols in a PLC-Zeta Knockout Mouse Model.” MOLECULAR HUMAN REPRODUCTION 26 (11): 801–815. doi:10.1093/molehr/gaaa060.
- Vancouver
- 1.Ferrer Buitrago M, Tilleman L, Thys V, Hachem A, Boel A, Van Nieuwerburgh F, et al. Comparative study of preimplantation development following distinct assisted oocyte activation protocols in a PLC-zeta knockout mouse model. MOLECULAR HUMAN REPRODUCTION. 2020;26(11):801–15.
- IEEE
- [1]M. Ferrer Buitrago et al., “Comparative study of preimplantation development following distinct assisted oocyte activation protocols in a PLC-zeta knockout mouse model,” MOLECULAR HUMAN REPRODUCTION, vol. 26, no. 11, pp. 801–815, 2020.
@article{8697128, abstract = {{Mammalian fertilization encompasses a series of Ca2+ oscillations initiated by the sperm factor phospholipase C zeta (PLC zeta). Some studies have shown that altering the Ca2+ oscillatory regime at fertilization affects preimplantation blastocyst development. However, assisted oocyte activation (AOA) protocols can induce oocyte activation in a manner that diverges profoundly from the physiological Ca2+ profiling. In our study, we used the newly developed PLC-null sperm to investigate the independent effect of AOA on mouse preimplantation embryogenesis. Based on previous findings, we hypothesized that AOA protocols with Ca2+ oscillatory responses might improve blastocyst formation rates and differing Ca2+ profiles might alter blastocyst transcriptomes. A total of 326 MII B6D2F1-oocytes were used to describe Ca2+ profiles and to compare embryonic development and individual blastocyst transcriptomes between four control conditions: C I (in-vivo fertilization), C2 (ICSI control sperm), C3 (parthenogenesis) and C4 (ICSI-PLC zeta-KO sperm) and four AOA groups: AOA1 (human recombinant PLC zeta, AOA2 (Sr2+), AOA3 (ionomycin) and AOA4 (TPEN). All groups revealed remarkable variations in their Ca2+ profiles; however, oocyte activation rates were comparable between the controls (91.1% +/- 13.8%) and AOA (86.9% +/- 11.1%) groups. AOA methods which enable Ca2+ oscillatory responses (AOA1: 41% and AOA2: 75%) or single Ca2+ transients (AOA3: 50%) showed no significantly different blastocyst rates compared to ICSI control group (C2: 70%). In contrast, we observed a significant decrease in compaction (53% vs. 83%) and blastocyst rates (41% vs. 70%) in the absence of an initial Ca2+ trigger (AOA4) compared with the C2 group. Transcription profiles did not identify significant differences in gene expression levels between the ICSI control group (C2) and the four AOA groups.}}, author = {{Ferrer Buitrago, Minerva and Tilleman, Laurentijn and Thys, Vanessa and Hachem, A and Boel, Annekatrien and Van Nieuwerburgh, Filip and Deforce, Dieter and Leybaert, Luc and De Sutter, Petra and Parrington, J. and Heindryckx, Björn}}, issn = {{1460-2407}}, journal = {{MOLECULAR HUMAN REPRODUCTION}}, keywords = {{assisted oocyte activation,calcium oscillations,blastocyst development,phospholipase C zeta,transcriptomics,animal model,PHOSPHOLIPASE-C-ZETA,EGG-ACTIVATION,CA2+ OSCILLATIONS,PARTHENOGENETIC ACTIVATION,FERTILIZATION FAILURE,CALCIUM OSCILLATIONS,ICSI,SIGNAL,INFERTILITY,INJECTION}}, language = {{eng}}, number = {{11}}, pages = {{801--815}}, title = {{Comparative study of preimplantation development following distinct assisted oocyte activation protocols in a PLC-zeta knockout mouse model}}, url = {{http://doi.org/10.1093/molehr/gaaa060}}, volume = {{26}}, year = {{2020}}, }
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