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Updated: Jul 2, 2026

Human Egg Maturity Assessment and Its Clinical Application
Published on: August 19, 2019
[Effect of protein kinase C in oocyte maturation, fertilization and preimplantation embryonic development]
Yajun Chen1, Shuqi Zhong, Xiuqing Feng
1Department of Histology and Embryology, Harbin Medical University, Harbin 150081, China.
Abstract:
Protein kinase C (PKC) family plays a critical role in many developmental events, including oocyte activation, completion of the second meiosis and initiation of the first mitosis, compaction, and blastocysts formation as well. But little is known of its many isozymes. Studies have shown that 10 isozymes of PKC and its anchor protein, RACK, are expressed in the course from 2 cell stage through blastocyst stage in mouse. We reviewed here the recent studies on the location pattern and expression levels of different PKC isozymes. Those studies indicated that the isozymes were very important for every stage of preimplantation embryonic development, especially at the early 4-cell stage. Some are increased temporarily in nucleus, which indicated that they might control and regulate the remolding of embryonic nucleus. We also analyzed the possible functions of PKCs in the somatic nuclear transferred embryos.
Insights
Protein kinase C (PKC) isozymes are crucial for mouse preimplantation embryonic development. Their expression patterns and nuclear localization at the 4-cell stage suggest key roles in embryonic nuclear remodeling and somatic nuclear transfer.
Area of Science:
- Developmental Biology
- Cell Signaling
- Molecular Embryology
Background:
- Protein kinase C (PKC) family is vital for embryonic development, including oocyte activation, meiosis, mitosis, and blastocyst formation.
- While the PKC family's importance is recognized, the specific roles of its numerous isozymes during early mammalian development remain largely uncharacterized.
- Ten PKC isozymes and their anchor protein, RACK, are expressed from the 2-cell to blastocyst stages in mouse embryos.
Purpose of the Study:
- To review recent findings on the localization patterns and expression levels of various PKC isozymes during mouse preimplantation development.
- To elucidate the critical roles of specific PKC isozymes in key embryonic developmental stages, particularly the early 4-cell stage.
- To analyze the potential functions of PKC isozymes in the context of somatic nuclear transferred embryos.
Main Methods:
- Review of recent scientific literature focusing on PKC isozyme expression and localization in mouse embryos.
- Analysis of expression data across different preimplantation stages (2-cell to blastocyst).
- Investigation of nuclear translocation patterns of specific PKC isozymes.
Main Results:
- PKC isozymes are expressed throughout mouse preimplantation development, with significant roles observed at every stage.
- Expression levels and localization patterns vary among different PKC isozymes, highlighting stage-specific functions.
- A notable increase in nuclear localization of certain PKC isozymes was observed at the early 4-cell stage, suggesting involvement in nuclear remodeling.
Conclusions:
- PKC isozymes are essential regulators of mouse preimplantation embryonic development, with critical functions at multiple stages.
- The dynamic expression and nuclear localization of PKC isozymes, especially at the 4-cell stage, underscore their importance in embryonic genome activation and nuclear reprogramming.
- Understanding PKC isozyme roles provides insights into developmental processes and potential applications in assisted reproductive technologies, including somatic nuclear transfer.
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