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.
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
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
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
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
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
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