Presence and dynamic redistribution of type I inositol 1,4,5-trisphosphate receptors in human oocytes and embryos during in-vitro maturation, fertilization and early cleavage divisions

• Published in: Molecular human reproduction 1999-05, Vol.5 (5), p.441-451
• Main Authors: Goud, P.T., Goud, A.P., Van Oostveldt, P., Dhont, M.
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Blastomeres - metabolism; Blotting, Western; calcium channels; Calcium Channels - metabolism; Cricetinae; Embryo, Mammalian - cytology; Embryo, Mammalian - metabolism; embryogenesis; Female; Fertilization in Vitro; Fundamental and applied biological sciences. Psychology; Humans; Image Enhancement; immunohistochemistry; Immunohistochemistry - methods; Inositol 1,4,5-Trisphosphate Receptors; inositol trisphosphate; Male; Mammalian female genital system; Meiosis; Metaphase; Microscopy, Confocal - methods; Morphology. Physiology; oocytes; Oocytes - cytology; Oocytes - metabolism; Receptors, Cytoplasmic and Nuclear - metabolism; Vertebrates: reproduction; Zygote
• ISSN: 1360-9947; 1460-2407; 1460-2407
• DOI: 10.1093/molehr/5.5.441

We studied the presence and distribution of the intracellular calcium channel regulating type I inositol 1,4,5-trisphosphate receptors (IP3R) in human immature and mature oocytes, pronuclear zygotes and cleaved embryos using a specific antibody. Two approaches were used: (i) fluorescence immunocytochemistry using a confocal laser scanning microscope (CLSM) and (ii) Western blotting. With confocal microscopy, the receptors were found in the oocytes, fertilized zygotes as well as cleaved embryos at all stages studied. The pattern and distribution of the receptor staining in the oocytes changed gradually from a diffuse granular patchy one at the germinal vesicle (GV) stage to a reticular and predominantly peripheral one through the metaphase I and metaphase II (MII) stages. After fertilization, the distribution changed gradually to both, peripheral and central in the zygotes and early 2–4-cell embryos and predominantly perinuclear in the 6–8-cell embryos. Furthermore, an overall increase in the staining intensity was observed from GV to MII stage oocytes and from zygotes to 6–8-cell embryos. We also studied the spatial distribution of the receptor in detail by constructing three-dimensional images from the serial optical sections obtained on the CLSM. Peculiar peripheral aggregates of receptor clusters were noted in the MII stage oocytes, zygotes and some blastomeres from early cleaved embryos. Finally, Western blots performed on the extracts of 72 in-vitro matured oocytes and 50 spare cleavage stage embryos showed positive bands at ~260 kDa. These findings coincide with and thus possibly represent the dynamic changes occurring in the cellular Ca2+ release systems through oocyte maturation, fertilization and early embryogenesis. Thus, type I IP3R are likely to play a role during these stages of early development in the human.