Effects of in vitro fertilization and embryo culture on TRP53 and Bax expression in B6 mouse embryos

被引:32
作者
Chandrakanthan, Vashe
Li, Aiqing
Chami, Omar
O'Neill, Christopher [1 ]
机构
[1] Univ Sydney, Royal N Shore Hosp, Discipline Physiol, St Leonards, NSW 2065, Australia
[2] Univ Sydney, Royal N Shore Hosp, Discipline Med, St Leonards, NSW 2065, Australia
关键词
D O I
10.1186/1477-7827-4-61
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
In the mouse, embryo culture results in a characteristic phenotype of retarded embryo preimplantation development and reduced numbers of cells within embryos. The expression of TRP53 is central to the regulation of the cell's capacity to proliferate and survive. In this study we found that Trp53 mRNA is expressed throughout the preimplantation stage of development. Levels of TRP53 protein expression were low during the cleavage stages and increased at the morula and blastocyst stages in B6 embryos collected from the reproductive tract. Embryos collected at the zygote stage and cultured for 96 h also showed low levels of TRP53 expression at precompaction stages. There were higher levels of TRP53 in cultured morula and the level in cultured blastocysts was clearly increased above blastocysts collected directly from the uterus. Immunolocalization of TRP53 showed that its increased expression in cultured blastocysts corresponded with a marked accumulation of TRP53 within the nuclei of embryonic cells. This pattern of expression was enhanced in embryos produced by in vitro fertilization and subjected to culture. The TRP53 was transcriptionally active since culture also induced increased expression of Bax, yet this did not occur in embryos lacking Trp53 (Trp53-/-). The rate of development of Trp53-/- zygotes to the blastocyst stage was not different to wildtype controls when embryos were cultured in groups of ten but was significantly faster when cultured individually. The results show that zygote culture resulted in the accumulation of transcription activity of TRP53 in the resulting blastocysts. This accounts for the adverse effects of culture of embryos individually, but does not appear to be the sole cause of the retarded preimplantation stage growth phenotype associated with culture in vitro.
引用
收藏
页数:10
相关论文
共 30 条
[1]
The p53 network [J].
Agarwal, ML ;
Taylor, WR ;
Chernov, MV ;
Chernova, OB ;
Stark, GR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :1-4
[2]
A study of the nature of embryonic lethality in LIS1-/- mice [J].
Cahana, A ;
Jin, XL ;
Reiner, O ;
Wynshaw-Boris, A ;
O'Neill, C .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2003, 66 (02) :134-142
[3]
DEVELOPMENT OF MOUSE EMBRYOS INVITRO IS AFFECTED BY STRAIN AND CULTURE-MEDIUM [J].
DANDEKAR, PV ;
GLASS, RH .
GAMETE RESEARCH, 1987, 17 (04) :279-285
[4]
Dobyns WB, 1992, NATURE, V358, P15
[5]
Mdm2 association with p53 targets its ubiquitination [J].
Fuchs, SY ;
Adler, V ;
Buschmann, T ;
Wu, XW ;
Ronai, Z .
ONCOGENE, 1998, 17 (19) :2543-2547
[6]
Hardy K, 1999, REV REPROD, V4, P125
[7]
From cell death to embryo arrest: Mathematical models of human preimplantation embryo development [J].
Hardy, K ;
Spanos, S ;
Becker, D ;
Iannelli, P ;
Winston, RML ;
Stark, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (04) :1655-1660
[8]
The p53QS transactivation-deficient mutant shows stress-specific apoptotic activity and induces embryonic lethality [J].
Johnson, TM ;
Hammond, EM ;
Giaccia, A ;
Attardi, LD .
NATURE GENETICS, 2005, 37 (02) :145-152
[9]
RESCUE OF EMBRYONIC LETHALITY IN MDM2-DEFICIENT MICE BY ABSENCE OF P53 [J].
JONES, SN ;
ROE, AE ;
DONEHOWER, LA ;
BRADLEY, A .
NATURE, 1995, 378 (6553) :206-208
[10]
Jurisicova A, 1998, MOL REPROD DEV, V51, P243, DOI 10.1002/(SICI)1098-2795(199811)51:3&lt