Literature DB >> 15831287

Increases in phosphorylation of SAPK/JNK and p38MAPK correlate negatively with mouse embryo development after culture in different media.

Yingchun Wang1, Elizabeth E Puscheck, Jennifer J Lewis, Anna B Trostinskaia, Fangfei Wang, Daniel A Rappolee.   

Abstract

OBJECTIVE: To test whether signal transduction proteins that mediate stress may be used to detect responses of embryos to different media in a prospective randomized study.
DESIGN: Controlled laboratory study.
SETTING: None. PATIENT(S): None. INTERVENTION(S): Mouse embryos isolated at E3.5 (3.5 days after fertilization) or E1.5 were cultured in different media for 24 hours or 72 hours, respectively. Expression of p38 mitogen activated protein kinases (MAPKs) and stress-activated protein kinase/Jun kinase (SAPK/JNK) phosphoproteins in the mouse embryo and their correlation with preimplantation development were studied. MAIN OUTCOME MEASURE(S): [1] In E3.5 embryos, SAPK/JNK and p38MAPK are phosphorylated at different levels in different media after 24 hours, with Ham's F10+BSA and M-16 having the highest intensity of both SAPK/JNK and p38MAPK phosphorylation and Quinn's cleavage medium and potassium simplex optimized medium supplemented with amino acids (KSOM+AA) the lowest intensity. [2] The stress-induced increase in phosphorylation of SAPK/JNK and p38MAPK appears to be post-translational in embryos. [3] The intensity of SAPK/JNK phosphorylation measured at E1.5+72 hours culture is inversely correlated with 4-cell/compaction rate, morula formation rate, blastocyst formation rate, and hatching rate. RESULT(S): SAPK/JNK and p38MAPK phosphoprotein levels, but not all forms of protein, are affected during culture of preimplantation embryos in seven different media. During culture, the rate of progress to four developmental events was assayed and each rate was inversely proportional to the level of SAPK/JNK phosphorylation measured by immunocytochemical means or Western blot analysis at the end of culture. CONCLUSION(S): Culture stresses embryos; different media exert different levels of stress on the embryos. There is a negative correlation between the amount of stress and the development rate. Taken together, the data suggest that SAPK/JNK phosphorylation may constitute a measure of homeostatic response to negative stimuli of media.

Entities:  

Keywords:  NASA Discipline Developmental Biology; Non-NASA Center

Mesh:

Substances:

Year:  2005        PMID: 15831287     DOI: 10.1016/j.fertnstert.2004.08.038

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  24 in total

1.  Oxygen levels that optimize TSC culture are identified by maximizing growth rates and minimizing stress.

Authors:  S Zhou; Y Xie; E E Puscheck; D A Rappolee
Journal:  Placenta       Date:  2011-04-21       Impact factor: 3.481

2.  Dynamics of protein phosphorylation during meiotic maturation.

Authors:  Lynda K McGinnis; David F Albertini
Journal:  J Assist Reprod Genet       Date:  2010-02-20       Impact factor: 3.412

3.  When stresses collide.

Authors:  Awoniyi O Awonuga; Yu Yang; Daniel A Rappolee
Journal:  Biol Reprod       Date:  2013-09-27       Impact factor: 4.285

4.  Commonly used fertility drugs, a diet supplement, and stress force AMPK-dependent block of stemness and development in cultured mammalian embryos.

Authors:  Alan Bolnick; Mohammed Abdulhasan; Brian Kilburn; Yufen Xie; Mindie Howard; Paul Andresen; Alexandra M Shamir; Jing Dai; Elizabeth E Puscheck; Daniel A Rappolee
Journal:  J Assist Reprod Genet       Date:  2016-05-26       Impact factor: 3.412

5.  Two-cell embryos are more sensitive than blastocysts to AMPK-dependent suppression of anabolism and stemness by commonly used fertility drugs, a diet supplement, and stress.

Authors:  Alan Bolnick; Mohammed Abdulhasan; Brian Kilburn; Yufen Xie; Mindie Howard; Paul Andresen; Alexandra M Shamir; Jing Dai; Elizabeth E Puscheck; Eric Secor; Daniel A Rappolee
Journal:  J Assist Reprod Genet       Date:  2017-09-15       Impact factor: 3.412

6.  The phosphoinositide kinase PIKfyve is vital in early embryonic development: preimplantation lethality of PIKfyve-/- embryos but normality of PIKfyve+/- mice.

Authors:  Ognian C Ikonomov; Diego Sbrissa; Khortnal Delvecchio; Yufen Xie; Jian-Ping Jin; Daniel Rappolee; Assia Shisheva
Journal:  J Biol Chem       Date:  2011-02-24       Impact factor: 5.157

Review 7.  Benzopyrene and experimental stressors cause compensatory differentiation in placental trophoblast stem cells.

Authors:  Daniel A Rappolee; Awoniyi O Awonuga; Elizabeth E Puscheck; Sichang Zhou; Yufen Xie
Journal:  Syst Biol Reprod Med       Date:  2010-04       Impact factor: 3.061

8.  Benzo(a)pyrene causes PRKAA1/2-dependent ID2 loss in trophoblast stem cells.

Authors:  Yufen Xie; Mazen E Abdallah; Awoniyi O Awonuga; Jill A Slater; Elizabeth E Puscheck; Dan A Rappolee
Journal:  Mol Reprod Dev       Date:  2010-06       Impact factor: 2.609

9.  CoQ10 increases mitochondrial mass and polarization, ATP and Oct4 potency levels, and bovine oocyte MII during IVM while decreasing AMPK activity and oocyte death.

Authors:  M K Abdulhasan; Q Li; J Dai; H M Abu-Soud; E E Puscheck; D A Rappolee
Journal:  J Assist Reprod Genet       Date:  2017-09-12       Impact factor: 3.412

10.  Stress induces AMPK-dependent loss of potency factors Id2 and Cdx2 in early embryos and stem cells [corrected].

Authors:  Yufen Xie; Awoniyi Awonuga; Jian Liu; Edmond Rings; Elizabeth Ella Puscheck; Daniel A Rappolee
Journal:  Stem Cells Dev       Date:  2013-03-11       Impact factor: 3.272

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