The effect of three-dimensional demineralized bone matrix on in vitro cumulus-free oocyte maturation

Biomaterials

Volumn 28, Issue 21, 2007, Pages 3198-3207

  Ma, Suofeng ^a   Lin, Hang ^a,b   Miao, Yiliang ^b,c   Liu, Xinyong ^d   Wang, Bin ^a,b   Dai, Jianwu ^a  

^a INSTITUTE OF GENETICS AND DEVELOPMENTAL BIOLOGY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c INSTITUTE OF ZOOLOGY   (China)

^d Tai'an Central Hospital   (China)

Author keywords

Co culture; Demineralized bone matrix; In vitro maturation; Oocyte

Indexed keywords

BIOMATERIALS; CELL CULTURE; COLLAGEN; GENES; THREE DIMENSIONAL;

CO CULTURE; DEMINERALIZED BONE MATRIX (DBM); IN VITRO MATURATION; OOCYTE MATURATION;

BONE;

BIOMATERIAL; COLLAGEN; MATURATION PROMOTING FACTOR; SCAFFOLD PROTEIN;

ANIMAL CELL; ARTICLE; BONE DEMINERALIZATION; BONE MATRIX; BRAIN CORTEX; CELL STRUCTURE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; CUMULUS OOPHORUS; FERTILIZATION IN VITRO; GRANULE CELL; IN VIVO CULTURE; NONHUMAN; OOCYTE MATURATION; PREIMPLANTATION EMBRYO; PRIORITY JOURNAL; THREE DIMENSIONAL IMAGING; ZONA PELLUCIDA;

ANIMALS; BIOCOMPATIBLE MATERIALS; BONE DEMINERALIZATION TECHNIQUE; BONE MATRIX; CATTLE; CELLS, CULTURED; CHROMOSOMES, MAMMALIAN; COCULTURE TECHNIQUES; COLLAGEN; CYTOPLASMIC GRANULES; FEMALE; FERTILIZATION IN VITRO; FIBROBLASTS; FORMAZANS; MATURATION-PROMOTING FACTOR; MEIOSIS; MICE; OOCYTES; OVARY; PARTHENOGENESIS; POROSITY; STRONTIUM; TETRAZOLIUM SALTS; ZONA PELLUCIDA;

MUS;

EID: 34247630227     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2007.03.007     Document Type: Article

References (50)

1. Mermillod P., Oussaid B., and Cognie Y. Aspects of follicular and oocyte maturation that affect the developmental potential of embryos. J Reprod Fertil Suppl 54 (1999) 449-460
2. Cha K.Y., and Chian R.C. Maturation in vitro of immature human oocytes for clinical use. Hum Reprod Update 4 2 (1998) 103-120
3. Hardy K., Wright C.S., Franks S., and Winston R.M. In vitro maturation of oocytes. Br Med Bull 56 3 (2000) 588-602
4. Trounson A., Anderiesz C., and Jones G. Maturation of human oocytes in vitro and their developmental competence. Reproduction 121 1 (2001) 51-75
5. Gosden R., Krapez J., and Briggs D. Growth and development of the mammalian oocyte. Bioessays 19 10 (1997) 875-882
6. van de Sandt J.J., Schroeder A.C., and Eppig J.J. Culture media for mouse oocyte maturation affect subsequent embryonic development. Mol Reprod Dev 25 2 (1990) 164-171
7. Sutton M.L., Gilchrist R.B., and Thompson J.G. Effects of in-vivo and in-vitro environments on the metabolism of the cumulus-oocyte complex and its influence on oocyte developmental capacity. Hum Reprod Update 9 1 (2003) 35-48
8. Combelles C.M., Fissore R.A., Albertini D.F., and Racowsky C. In vitro maturation of human oocytes and cumulus cells using a co-culture three-dimensional collagen gel system. Hum Reprod 20 5 (2005) 1349-1358
9. Eppig J.J., Pendola F.L., Wigglesworth K., and Pendola J.K. Mouse oocytes regulate metabolic cooperativity between granulosa cells and oocytes: amino acid transport. Biol Reprod 73 2 (2005) 351-357
10. Miao Y.L., Liu X.Y., Qiao T.W., Miao D.Q., Luo M.J., and Tan J.H. Cumulus cells accelerate aging of mouse oocytes. Biol Reprod 73 5 (2005) 1025-1031
11. Eppig J.J. The relationship between cumulus cell-oocyte coupling, oocyte meiotic maturation, and cumulus expansion. Dev Biol 89 1 (1982) 268-272
12. Eppig J.J. Intercommunication between mammalian oocytes and companion somatic cells. Bioessays 13 11 (1991) 569-574
13. Buccione R., Schroeder A.C., and Eppig J.J. Interactions between somatic cells and germ cells throughout mammalian oogenesis. Biol Reprod 43 4 (1990) 543-547
14. Tanghe S., Van Soom A., Nauwynck H., Coryn M., and de Kruif A. Minireview: functions of the cumulus oophorus during oocyte maturation, ovulation, and fertilization. Mol Reprod Dev 61 3 (2002) 414-424
15. Miki H., Ogonuki N., Inoue K., Baba T., and Ogura A. Improvement of cumulus-free oocyte maturation in vitro and its application to microinsemination with primary spermatocytes in mice. J Reprod Dev 52 2 (2006) 239-248
16. Combelles C.M., Cekleniak N.A., Racowsky C., and Albertini D.F. Assessment of nuclear and cytoplasmic maturation in in-vitro matured human oocytes. Hum Reprod 17 4 (2002) 1006-1016
17. Eppig J.J. A comparison between oocyte growth in coculture with granulosa cells and oocytes with granulosa cell-oocyte junctional contact maintained in vitro. J Exp Zool 209 2 (1979) 345-353
18. Sirard M.A., and Bilodeau S. Effects of granulosa cell co-culture on in-vitro meiotic resumption of bovine oocytes. J Reprod Fertil 89 2 (1990) 459-465
19. Moor R.M., Mattioli M., Ding J., and Nagai T. Maturation of pig oocytes in vivo and in vitro. J Reprod Fertil Suppl 40 (1990) 197-210
20. Abbott A. Cell culture: biology's new dimension. Nature 424 6951 (2003) 870-872
21. Bissell M.J. Glandular structure and gene expression. Lessons from the mammary gland. Ann NY Acad Sci 842 (1998) 1-6
22. Weaver V.M., Petersen O.W., Wang F., Larabell C.A., Briand P., Damsky C., et al. Reversion of the malignant phenotype of human breast cells in three-dimensional culture and in vivo by integrin blocking antibodies. J Cell Biol 137 1 (1997) 231-245
23. Cukierman E., Pankov R., Stevens D.R., and Yamada K.M. Taking cell-matrix adhesions to the third dimension. Science 294 5547 (2001) 1708-1712
24. Cukierman E., Pankov R., and Yamada K.M. Cell interactions with three-dimensional matrices. Curr Opin Cell Biol 14 5 (2002) 633-639
25. Huet C., Pisselet C., Mandon-Pepin B., Monget P., and Monniaux D. Extracellular matrix regulates ovine granulosa cell survival, proliferation and steroidogenesis: relationships between cell shape and function. J Endocrinol 169 2 (2001) 347-360
26. Hwang D.H., Kee S.H., Kim K., Cheong K.S., Yoo Y.B., and Lee B.L. Role of reconstituted basement membrane in human granulosa cell culture. Endocr J 47 2 (2000) 177-183
27. Richardson M.C., Slack C., and Stewart I.J. Rearrangement of extracellular matrix during cluster formation by human luteinising granulosa cells in culture. J Anat 196 Pt 2 (2000) 243-248
28. Torrance C., Telfer E., and Gosden R.G. Quantitative study of the development of isolated mouse pre-antral follicles in collagen gel culture. J Reprod Fertil 87 1 (1989) 367-374
29. Hirao Y., Nagai T., Kubo M., Miyano T., Miyake M., and Kato S. In vitro growth and maturation of pig oocytes. J Reprod Fertil 100 2 (1994) 333-339
30. Osaki S., Matsumura K., Yamamoto K., Miyano T., Miyake M., and Kato S. Fertilization of bovine oocytes grown in vitro. Reprod Fertil Dev 9 8 (1997) 781-787
31. Abir R., Roizman P., Fisch B., Nitke S., Okon E., Orvieto R., et al. Pilot study of isolated early human follicles cultured in collagen gels for 24 h. Hum Reprod 14 5 (1999) 1299-1301
32. Kreeger P.K., Deck J.W., Woodruff T.K., and Shea L.D. The in vitro regulation of ovarian follicle development using alginate-extracellular matrix gels. Biomaterials 27 5 (2006) 714-723
33. Schouten C.C., Hartman E.H., Spauwen P.H., and Jansen J.A. DBM induced ectopic bone formation in the rat: the importance of surface area. J Mater Sci Mater Med 16 2 (2005) 149-152
34. Ma S.F., Liu X.Y., Miao D.Q., Han Z.B., Zhang X., Miao Y.L., et al. Parthenogenetic activation of mouse oocytes by strontium chloride: a search for the best conditions. Theriogenology 64 5 (2005) 1142-1157
35. Quinn P., Barros C., and Whittingham D.G. Preservation of hamster oocytes to assay the fertilizing capacity of human spermatozoa. J Reprod Fertil 66 1 (1982) 161-168
36. Liu X.Y., Mal S.F., Miao D.Q., Liu D.J., Bao S., and Tan J.H. Cortical granules behave differently in mouse oocytes matured under different conditions. Hum Reprod 20 12 (2005) 3402-3413
37. Ludwig S.C., and Boden S.D. Osteoinductive bone graft substitutes for spinal fusion: a basic science summary. Orthop Clin North Am 30 4 (1999) 635-645
38. Chen B., Lin H., Zhao Y., Wang B., Zhao Y., Liu Y., et al. Activation of demineralized bone matrix by genetically engineered human bone morphogenetic protein-2 with a collagen binding domain derived from von Willebrand factor propolypeptide. J Biomed Mater Res A (2006)
39. Ducibella T., Duffy P., and Buetow J. Quantification and localization of cortical granules during oogenesis in the mouse. Biol Reprod 50 3 (1994) 467-473
40. Zamboni L. Ultrastructure of mammalian oocytes and ova. Biol Reprod Suppl 2 (1970) 44-63
41. Damiani P., Fissore R.A., Cibelli J.B., Long C.R., Balise J.J., Robl J.M., et al. Evaluation of developmental competence, nuclear and ooplasmic maturation of calf oocytes. Mol Reprod Dev 45 4 (1996) 521-534
42. Miyara F., Aubriot F.X., Glissant A., Nathan C., Douard S., Stanovici A., et al. Multiparameter analysis of human oocytes at metaphase II stage after IVF failure in non-male infertility. Hum Reprod 18 7 (2003) 1494-1503
43. Ducibella T., Anderson E., Albertini D.F., Aalberg J., and Rangarajan S. Quantitative studies of changes in cortical granule number and distribution in the mouse oocyte during meiotic maturation. Dev Biol 130 1 (1988) 184-197
44. Ducibella T., Kurasawa S., Rangarajan S., Kopf G.S., and Schultz R.M. Precocious loss of cortical granules during mouse oocyte meiotic maturation and correlation with an egg-induced modification of the zona pellucida. Dev Biol 137 1 (1990) 46-55
45. Ducibella T., Duffy P., Reindollar R., and Su B. Changes in the distribution of mouse oocyte cortical granules and ability to undergo the cortical reaction during gonadotropin-stimulated meiotic maturation and aging in vivo. Biol Reprod 43 5 (1990) 870-876
46. Ducibella T., Kurasawa S., Duffy P., Kopf G.S., and Schultz R.M. Regulation of the polyspermy block in the mouse egg: maturation-dependent differences in cortical granule exocytosis and zona pellucida modifications induced by inositol 1,4,5-trisphosphate and an activator of protein kinase C. Biol Reprod 48 6 (1993) 1251-1257
47. Ducibella T., and Buetow J. Competence to undergo normal, fertilization-induced cortical activation develops after metaphase I of meiosis in mouse oocytes. Dev Biol 165 1 (1994) 95-104
48. Okada A., Yanagimachi R., and Yanagimachi H. Development of a cortical granule-free area of cortex and the perivitelline space in the hamster oocyte during maturation and following ovulation. J Submicrosc Cytol 18 2 (1986) 233-247
49. Okada A., Inomata K., and Nagae T. Spontaneous cortical granule release and alteration of zona pellucida properties during and after meiotic maturation of mouse oocytes. Anat Rec 237 4 (1993) 518-526
50. Schroeder A.C., Schultz R.M., Kopf G.S., Taylor F.R., Becker R.B., and Eppig J.J. Fetuin inhibits zona pellucida hardening and conversion of ZP2 to ZP2f during spontaneous mouse oocyte maturation in vitro in the absence of serum. Biol Reprod 43 5 (1990) 891-897