Vet Med - Czech, 2010, 55(10):512-521 | DOI: 10.17221/2941-VETMED

Assessment of transcript and protein levels contributing to cell cycle control and gap junction connections in morphologically variable groups of porcine cumulus-oocyte complexes

P. Antosik1, B. Kempisty2, M. Jackowska1, H. Piotrowska3, D. Bukowska1, M. Wozna1, M. Lianeri1, K.-P. Brussow4, J.M. Jaskowski2
1 Department of Veterinary, University of Life Sciences, Poznan, Poland
2 Department of Histology and Embryology, University of Medical Sciences, Poznan, Poland
3 Department of Toxicology, University of Medical Sciences, Poznan, Poland
4 Department of Reproductive Biology, FBN Research Institute for the Biology of Farm Animals, Dummerstorf, Germany

Oocytes and somatic cumulus cells are connected by an extensive network of gap junctions. These connections contribute in a major way to oocyte maturation and developmental competence. Cumulus-oocyte complexes (COCs) were cultured in standard porcine IVM culture medium (TCM 199) for 44 h. The morphological classification of COCs is based on the number of cumulus cell layers and the degree of their compaction, as well as on cytoplasm composition (homogenous, heterogeneous). The obtained COCs were divided into four grades according to this classification system. By assessing the activity of glucose-6-phosphate dehydrogenase (G6PDH) using the brilliant cresyl blue (BCB) test, real-time quantitative PCR (RQ-PCR) reaction methods and confocal microscopic observations, we determined the transcript levels of connexins 43 and 45, cyclin dependent kinases (cdk5 and cdk5r), and cdk inhibitors 1 and 3 (p27kip1 and cdkn3) as well as cdk4 protein in morphologically different groups of porcine oocytes isolated from puberal gilts. To assess their nuclear status the completely denuded oocytes were subjected to DAPI staining. We found statistically increased cdkn3, cdk5 and connexin 45 mRNA levels in oocytes graded as I as compared to II, III, and IV. The cdkn1, cdk5r and connexin 43 transcript contents were higher only when comparing between oocytes graded as I, III and IV. The cdk4 protein in oocytes graded I and II is localized mainly in the zona pellucida, although in grade III COCs the expression of this protein is decreased and observed only in the cytoplasm. Grade IV COCs do not demonstrate a significant presence of cdk4 protein. With regards to nuclear maturation, the percentage of MII stage oocytes was significantly (P < 0.05) higher in grade I and II oocytes as compared to grade III and IV oocytes. Our results demonstrate for the first time that cdk4 protein localization and all of the investigated transcript levels are associated with COC morphology and may be related to further maturation ability as well as developmental competence of oocytes.

Keywords: pig; oocyte; connexins; cyclin-dependent kinases

Published: October 31, 2010  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Antosik P, Kempisty B, Jackowska M, Piotrowska H, Bukowska D, Wozna M, et al.. Assessment of transcript and protein levels contributing to cell cycle control and gap junction connections in morphologically variable groups of porcine cumulus-oocyte complexes. Vet Med - Czech. 2010;55(10):512-521. doi: 10.17221/2941-VETMED.
Download citation

References

  1. Ackert CL, Gittens JE, O'Brien MJ, Eppig JJ, Kidder GM (2001): Intercellular communication via connexin43 gap junctions is required for ovarian folliculogenesis in the mouse. Developmnetal Biology 233, 258-270. Go to original source... Go to PubMed...
  2. Akamatsu E, Tanaka T, Kato JY (1998): Transcription factor E2F and cyclin E-Cdk2 complex cooperate to induce chromosomal DNA replication in Xenopus oocytes. The Journal of Biological Chemistry 273, 16494-16500. Go to original source... Go to PubMed...
  3. Alm H, Torner H, Loehrke B, Viergutz T, Ghoneim IM, Kanitz W (2005): Bovine blastocyst development rate in vitro is influenced by selection of oocytes by brillant cresyl blue staining before IVM as indicator for glucose-6-phosphate dehydrogenase activity. Theriogenology 63, 2194-2205. Go to original source... Go to PubMed...
  4. Assidi M, Dufort I, Ali A, Hamel M, Algriany O, Dielemann S, Sirard MA (2008): Identification of potential markers of oocyte competence expressed in bovine cumulus cells matured with follicle-stimulating hormone and/or phorbol myristate acetate in vitro. Biology of Reproduction 79, 209-222. Go to original source... Go to PubMed...
  5. Balaban B, Urman B (2006): Effect of oocyte morphology on embryo development and implantation. Reproductive Biomedicine Online12, 608-615. Go to original source...
  6. Bhojwani S, Alm H, Torner H, Kanitz W, Poehland R (2007): Selection of developmentally competent oocytes through brilliant cresyl blue stain enhances blastocyst development rate after bovine nuclear transfer. Theriogenology 67, 341-345. Go to original source... Go to PubMed...
  7. Calder MD, Caveney AN, Smith LC, Watson AJ (2003): Responsiveness of bovine cumulus-oocyte-complexes (COC) to porcine and recombinant human FSH, and the effect of COC quality on gonadotropin receptor and Cx43 marker gene mRNAs during maturation in vitro. Reproductive Biology and Endocrinology 11, 1-14. Go to original source... Go to PubMed...
  8. Carabatsos MJ, Sellitto C, Goodenough DA, Albertini DF (2000): Oocyte-granulosa cell heterologous gap junctions are required for the coordination of nuclear and cytoplasmic meiotic competence. Developmental Biology 226, 167-179. Go to original source... Go to PubMed...
  9. Ciray HN, Coban O, Bayram A, Kizilkanat A, Bahceci M (2008): Preliminary study of embryo development following assessment of male and female gametes. Reproductive Biomedicine Online 16, 875-880. Go to original source... Go to PubMed...
  10. Combelles CM, Racowsky C (2005): Assessment and optimization of oocyte quality during assisted reproductive technology treatment. Seminars in Reproductive Medicine 23, 277-284. Go to original source... Go to PubMed...
  11. Egerszegi I, Alm H, Rátky J, Heleil B, Brussow KP, Torner H (2010): Meiotic progression, mitochondrial features and fertilisation characteristics of porcine oocytes with different G6PDH activities. Reproducftion of Fertility and Development 22, 830-838. Go to original source... Go to PubMed...
  12. Feuerstein P, Cadoret V, Dalbies-Tran R, Guerif F, Bidault R, Royere D (2007): Gene expression in human cumulus cells: one approach to oocyte competence. Human Reproduction 22, 3069-3077. Go to original source... Go to PubMed...
  13. Font de Mora J, Uren A, Heidaran M, Santos E (1997): Biological activity of p27kip1 and its amino- and carboxy-terminal domains in G2/M transition of Xenopus oocytes. Oncogene 15, 2541-2551. Go to original source... Go to PubMed...
  14. Gittens JE, Kidder GM (2005): Differential contributions of connexin37 and connexin43 to oogenesis revealed in chimeric reaggregated mouse ovaries. Journal of Cell Science 118, 5071-5080. Go to original source... Go to PubMed...
  15. Jackowska M, Kempisty B, Antosik P, Bukowska D, Budna J, Lianeri M, Rosinska E, Wozna M, Jagodzinski PP, Jaskowski JM (2009): The morphology of porcine oocytes is associated with zona pellucida glycoprotein transcript contents. Reproductive Biology 9, 79-85. Go to original source... Go to PubMed...
  16. Kelly JM, Kleemann DO, Rudiger SR, Walker SK (2007): Effects of grade of oocyte-cumulus complex and the interactions between grades on the production of blastocysts in the cow, ewe and lamb. Reproduction in Domestic Animals 42, 577-582. Go to original source... Go to PubMed...
  17. Kempisty B, Antosik P, Bukowska D, Jackowska M, Lianeri M, Jaskowski JM, Jagodzinski PP (2008): Analysis of selected transcript levels in porcine spermatozoa, oocytes, zygotes and two-cell stage embryos. Reproduction, Fertility, and Development 20, 513-518. Go to original source... Go to PubMed...
  18. Kempisty B, Antosik P, Bukowska D, Jackowska M, Lianeri M, Jaskowski JM, Jagodzinski PP (2009): Assessment of zona pellucida glycoprotein and integrin transcript contents in porcine oocytes. Reproductive Biology 9, 71-80. Go to original source... Go to PubMed...
  19. Kohoutek J, Dvorak P, Hampl A (2004): Temporal distribution of CDK4, CDK6, D-type cyclins, and p27 in developing mouse oocytes. Biology of Reproduction 70, 139-145. Go to original source... Go to PubMed...
  20. Li TY, Colley D, Barr KJ, Yee SP, Kidder GM (2007): Rescue of oogenesis in Cx37-null mutant mice by oocytespecific replacement with Cx43. Journal of Cell Science 120, 4117-4125. Go to original source... Go to PubMed...
  21. Luciano AM, Modina S, Vassena R, Milanesi E, Lauria A, Gandolfi F (2004): Role of intracellular cyclic adenosine 3',5'-monophosphate concentration and oocyte-cumulus cells communications on the acquisition of the developmental competence during in vitro maturation of bovine oocyte. Biology of Reproduction 70, 465-472. Go to original source... Go to PubMed...
  22. Marchal R, Caillaud M, Martoriati A, Gerard N, Mermillod P, Goudet G (2003): Effect of growth hormone (GH) on in vitro nuclear and cytoplasmic oocyte maturation, cumulus expansion, hyaluronan synthases, and connexins 32 and 43 expression, and GH receptor messenger RNA expression in equine and porcine species. Bioliology of Reproduction 69, 1013-1022. Go to original source... Go to PubMed...
  23. Mermillod P, Dalbies-Tran R, Uzbekova S, Thelie A, Traverso JM, Perreau C, Papillier P, Monget P (2008): Factors affecting oocyte quality: who is driving the follicle? Reproduction in Domestic Animals 43 Suppl. 2, 393-400. Go to original source... Go to PubMed...
  24. Miyano T, Manabe N (2007): Oocyte growth and acquisition of meiotic competence. Society of Reproduction and Fertility 63 (Suppl.), 531-538.
  25. Motlik J, Pavlok A, Kubelka M, Kalous J, Kalab P (1998): Interplay between CDC2 kinase and MAP kinase pathway during maturation of mammalian oocytes. Theriogenology 49, 461-469. Go to original source... Go to PubMed...
  26. Obata Y, Maeda Y, Hatada I, Kono T (2007): Long-term effects of in vitro growth of mouse oocytes on their maturation and development. The Journal of Reproduction and Development 53, 1183-1190. Go to original source... Go to PubMed...
  27. Patrizio P, Fragouli E, Bianchi V, Borini A, Wells D (2007): Molecular methods for selection of the ideal oocyte. Reproductive Biomedicine Online, 15, 346- 353. Go to original source... Go to PubMed...
  28. Pujol M, Lopez-Bejar M, Paramio MT (2 0 0 4) : D e v e lo p mental competence of heifer oocytes selected using the brilliant cresyl blue (BCB) test. Theriogenology 61, 735-744. Go to PubMed...
  29. Rajareddy S, Reddy P, Du C, Liu L, Jagarlamudi K, Tang W, Shen Y, Berthet C, Peng SL, Kaldis P, Liu K(2007): p27kip1 (cyclin-dependent kinase inhibitor 1B) controls ovarian development by suppressing follicle endowment and activation and promoting follicle atresia in mice. Molecular Endocrinology 21, 2189-2202. Go to original source... Go to PubMed...
  30. Sasseville M, Gagnon MC, Guillemette C, Sullivan R, Gil
  31. Smith S., Everts RE, Sung LY, Du F, Page RL, Henderson B, Rodriguez-Zas SL, Nedambale TL, Renard JP, Lewin HA, Yang X, Tian XC (2009): Gene expression profilchrist RB, Richard FJ (2009): Regulation of gap junctions ing of single bovine embryos uncovers significant efin porcine cumulus-oocyte complexes: contributions fects of in vitro maturation, fertilization and culture. of granulosa cell contact, gonadotropins, and lipid rafts. Molecular Reproduction and Development 76, Molecular Endocrinology 23, 700-710. Go to original source... Go to PubMed...
  32. Sato E, Yokoo M (2005): Morphological and biochemical dynamics of porcine cumulus-oocyte complexes: role of cumulus expansion in oocyte maturation. Italian Journal of Anatomy and Embryology 110 (Suppl. 1), 205-217.
  33. Sato C, Shimada M, Mori T, Kumasako Y, Otsu E, Watanabe H, Utsunomiya T (2007): Assessment of human oocyte developmental competence by cumulus cell morphology and circulating hormone profile. Reproductive Biomedicine Online 14, 49-56. Go to original source... Go to PubMed...
  34. Shimada M, Maeda T, Terada T (2001): Dynamic changes of connexin-43, gap junctional protein, in outer layers of cumulus cells are regulated by PKC and PI 3-kinase during meiotic resumption in porcine oocytes. Biology of Reproduction 64, 1255-1263. Go to original source... Go to PubMed...
  35. Singh R, Sinclair KD (2007): Metabolomics: approaches to assessing oocyte and embryo quality. Theriogenology 68 (Suppl. 1), 56-62. 38-47. Go to original source... Go to PubMed...
  36. Thellin O, Zorzi W, Lakaye B, De Borman B, Coumans B, Hennen G, Grisar T, Igout A, Heinen E (1999): Housekeeping genes as internal standards: use and limits. Journal of Biotechnology 75, 291-295. Go to original source... Go to PubMed...
  37. Vozzi C, Formenton A, Chanson A, Senn A, Sahli R, Shaw P, Nicod P, Germond M, Haefliger JA (2001): Involvement of connexin 43 in meiotic maturation of bovine oocytes. Reproduction 122, 619-628. Go to original source... Go to PubMed...
  38. Wang Q, Sun QY (2007): Evaluation of oocyte quality: morphological, cellular and molecular predictors. Reproduction, Fertility, and Development 19, 1-12. Go to original source... Go to PubMed...
  39. Whitten SJ, Miller MA (2007): The role of gap junctions in Caenorhabditis elegans oocyte maturation and fertilization. Developmental Biology 301, 432-446. Go to original source... Go to PubMed...
  40. Wu YG, Liu Y, Zhou P, Lan GC, Han D, Miao DQ, Tan JH (2007): Selection of oocytes for in vitro maturation by brilliant cresyl blue staining: a study using the mouse model. Cell Research 17, 722-731. Go to original source... Go to PubMed...

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY NC 4.0), which permits non-comercial use, distribution, and reproduction in any medium, provided the original publication is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.