DOI QR코드

DOI QR Code

Effect of Arachidonic Acid on Production of Laminin and Connexin of Granulosa Cells from Chicken Pre-hierarchical Follicles

  • Jin, Yanmei (Key Laboratory of Animal Epidemic Etiology and Immunological Prevention of the Ministry of Agriculture College of Animal Sciences, Zhejiang University) ;
  • Tan, Tu Quang (Key Laboratory of Animal Epidemic Etiology and Immunological Prevention of the Ministry of Agriculture College of Animal Sciences, Zhejiang University) ;
  • Zhang, Caiqiao (Key Laboratory of Animal Epidemic Etiology and Immunological Prevention of the Ministry of Agriculture College of Animal Sciences, Zhejiang University)
  • 투고 : 2008.07.11
  • 심사 : 2008.11.27
  • 발행 : 2009.03.01

초록

Arachidonic acid (AA) is a polyunsaturated fatty acid that is a normal constituent of membrane lipids in animal cells. In addition to its role as a precursor of prostaglandins, AA itself may play an important role in the regulation of cell function. The effect of AA on functions of granulosa cells was investigated in pre-hierarchical small yellow follicles of laying hens. Immuno-cytochemical staining showed that AA ($10^{-7}-10^{-5}$ M) increased the expression of the extracellular matrix glycoprotein laminin, gap junction connexin 43 and protein kinase C (PKC). Therefore, mediated by the PKC signal pathway, AA may regulate the intercellular communication of granulosa cells and follicular development by increasing the expression of laminin and connexin.

키워드

참고문헌

  1. Ackert, C. L., J. E. Gittens, M. J. O'Brien, J. J. Eppig and G. M. Kidder. 2001. Intercellular communication via connexin 43 gap junctions is required for ovarian folliculogenesis in the mouse. Dev. Biol. 233:258-270 https://doi.org/10.1006/dbio.2001.0216
  2. Choi, K. M., J. K. Moon, S. H. Choi, K. S. Kim, Y. I. Choi, J. J. Kim and C. K. Lee. 2008. Differential expression of cytochrome P450 genes regulates the level of adipose arachidonic acid in Sus scrofa. Asian-Aust. J. Anim. Sci. 21:967-971
  3. Grazul-Bilska, A. T., L. P Reynolds and D. A. Redmer. 1997. Gap junctions in the ovaries. Biol. Reprod. 57:947-957 https://doi.org/10.1095/biolreprod57.5.947
  4. Harizi, H., J. B. Corcuff and N. Gualde. 2008. Arachidonic-acidderived eicosanoids: roles in biology and immunopathology. Trends Mol. Med. 14:461-469 https://doi.org/10.1016/j.molmed.2008.08.005
  5. Hertelendy, F., M. Moln$\acute{a}$rl and M. Jamaluddin. 1992. Dual action of arachidonic acid on calcium mobilization in avian granulosa cells. Mol. Cell. Endocrinol. 83:173-181 https://doi.org/10.1016/0303-7207(92)90157-2
  6. Jia, Y. and J. J. Turek. 2004. Polyenoic fatty acid ratios alter fibroblast collagen production via $PGE_{2}$ and PGE receptor subtype response. Exp. Biol. Med. 229:676-683
  7. Jin, Y. M., C. Q. Zhang, X. H. Lin and W. D. Zeng. 2006. Prostaglandin involvement in follicle-stimulating hormoneinduced proliferation of granulosa cells from chicken prehierarchical follicles. Prostag. Other Lipid Mediat. 81:45-54 https://doi.org/10.1016/j.prostaglandins.2006.07.002
  8. Jin, Y. M., C. Q. Zhang, W. D. Zeng, K Taya and T. Q. Tan. 2007. Interactive actions of prostaglandin and epidermal growth factor to enhance proliferation of granulosa cells from chicken prehierarchical follicles. Prostag. Other Lipid Mediat. 83:285-294 https://doi.org/10.1016/j.prostaglandins.2007.02.002
  9. Juneja, S. C., K. J. Barr, G. C. Enders and G. M. Kidde. 1999. Defects in the germ line and gonads of mice lacking connexin43. Biol. Reprod. 60:1263-1270 https://doi.org/10.1095/biolreprod60.5.1263
  10. Kariya, Y. and K. Miyazaki. 2004. The basement membrane protein laminin-5 acts as a soluble cell motility factor. Exp. Cell Res. 297:508-520 https://doi.org/10.1016/j.yexcr.2004.03.044
  11. Kolch, W., G. Heidecker, G. Kochs, R. Hummel, H. Vahidi, H. Mischak, G. Finkenzeller, D. Marme and U. R. Rapp. 1993. Protein kinase C alpha activates RAF-1 by direct phosphorylation. Nature 364:249-252 https://doi.org/10.1038/364249a0
  12. Lampe, P. D., E. M. TenBroek, J. M. Burt, W. E. Kurata, R. G. Johnson and A. F. Lau. 2000. Phosphorylation of connexin43 on serine368 by protein kinase C regulates gap junctional communication. J. Cell Biol. 149:1503-1512 https://doi.org/10.1083/jcb.149.7.1503
  13. Lester, D. S., C. Collin, R. Etcheberrigaray and D. L. Alkon. 1991. Arachidonic acid and diacylglycerol act synergistically to activate protein kinase C in vitro and in vivo. Biochem. Biophys. Res. Commun. 179:1522-1558 https://doi.org/10.1016/0006-291X(91)91745-X
  14. Liu, H. Y., C. Q. Zhang, C. T. Ge and J. X. Liu. 2007. Effects of daidzein on mRNA expression of gonadotropin receptors and P450 aromatase in ovarian follicles of white silky fowls. Asian-Aust. J. Anim. Sci. 20:1827-1831
  15. Liu, H. Y. and C. Q. Zhang. 2008. Effects of daidzein on messenger ribonucleic acid expression of gonadotropin receptors in chicken ovarian follicles. Poult. Sci. 87:541-545 https://doi.org/10.3382/ps.2007-00274
  16. Mecham, R. P. 1991. Receptors for laminin on mammalian cells. FASEB J. 5:2538-2546
  17. Melton, C. M., G. M. Zaunbrecher, G. Yoshizaki, R. Pati$\tilde{n}$o, S. Whisnant, A. Rendon and V. H. Lee. 2001. Expression of connexin 43 mRNA and protein in developing follicles of prepubertal porcine ovaries. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 130:43-55 https://doi.org/10.1016/S1096-4959(01)00403-1
  18. Mochizuki-Oda, N., M. Negishi, K. Mori and S. Ito. 1993. Arachidonic acid activates cation channels in bovine adrenal chromaffin cells. J. Neurochem. 61:1882-1890 https://doi.org/10.1111/j.1471-4159.1993.tb09830.x
  19. Musil, L. S. and D. A. Goodenough. 1991. Biochemical analysis of connexin43 intracellular transport, phosphorylation, and assembly into gap junctional plaques. J. Cell Biol. 115:1357-1374 https://doi.org/10.1083/jcb.115.5.1357
  20. Risek, B., S. Guthrie, N. Kumar and N. Gilula. 1990. Modulation of gap junction transcript and protein expression during pregnancy in the rat. J. Cell Biol. 110:269-282 https://doi.org/10.1083/jcb.110.2.269
  21. Rodgers, R. J., H. F. Irving-Rodgers and I. L. van Wezel. 2000. Extracellular matrix in ovarian follicles. Mol. Cell. Endocrinol. 163:73-79 https://doi.org/10.1016/S0303-7207(00)00219-7
  22. Sardesai, V. M. 1992. Biochemical and nutritional aspects of eicosanoids. J. Nutr. Biochem. 3:562-579 https://doi.org/10.1016/0955-2863(92)90050-S
  23. Vakonakis, I. and I. D Campbell. 2007. Extracellular matrix: from atomic resolution to ultrastructure. Cell Biol. 19:578-583 https://doi.org/10.1016/j.ceb.2007.09.005
  24. Verlengia, R., R. Gorjao, C. C. Kanunfre, S. Bordin, T. M. de Lima and R. Curi. 2003. Effect of arachidonic acid on proliferation, cytokines production and pleiotropic genes expression in Jurkat cells-A comparison with oleic acid. Life Sci. 73:2939-2951 https://doi.org/10.1016/j.lfs.2003.04.003
  25. Watkins, B. A., H. Xu and J. J. Turek. 1996. Linoleate impairs collagen synthesis in primary cultures of avian chondrocytes. Proc. Soc. Exp. Biol. Med. 212:153-159
  26. Zhao, Y. and M. R. Luck. 1995. Gene expression and protein distribution of collagen, fibronectin and laminin in bovine follicles and corpora lutea. J. Reprod. Fertil. 104:115-123 https://doi.org/10.1177/1933719107309818

피인용 문헌

  1. oocyte maturation and embryo development vol.34, pp.8, 2018, https://doi.org/10.1080/09513590.2018.1431770
  2. Role of Lipid Metabolism and Signaling in Mammalian Oocyte Maturation, Quality, and Acquisition of Competence vol.9, pp.None, 2009, https://doi.org/10.3389/fcell.2021.639704
  3. In vitro maturation using an agarose matrix with incorporated extracellular matrix proteins improves porcine oocyte developmental competence by enhancing cytoplasmic maturation vol.15, pp.10, 2021, https://doi.org/10.1002/term.3228
  4. An increase of phosphatidylcholines in follicular fluid implies attenuation of embryo quality on day 3 post-fertilization vol.19, pp.1, 2009, https://doi.org/10.1186/s12915-021-01118-w