Literature DB >> 1655543

Hydrogen peroxide as a mediator of programmed cell death in the blastocyst.

G B Pierce1, R E Parchment, A L Lewellyn.   

Abstract

Previous work identified in blastocele fluid a soluble activity which killed embryonal carcinoma cells with trophectodermal potential but not those with embryonic potential [35]. From use of a malignant caricature of the late blastocyst, this toxic activity was postulated to be H2O2 [8]. The purpose of this paper was to determine if blastocele fluid also contained amounts of H2O2 capable of mediating the preferential killing of malignant pretrophectodermal cells (ECa 247). We not only observed that blastocele fluid is not toxic for these cells in the presence of catalase, but that malignant cells with embryonic potential (P19) that normally survive exposure to blastocele fluid become sensitive to it if their intracellular glutathione levels are lowered. Thus, it is concluded that the blastocyst contains amounts of H2O2 toxic to malignant pretrophectodermal cells and that glutathione-dependent mechanisms protect malignant inner cell mass cells with embryonic potential. Apparently, H2O2 production and glutathione-dependent protection mechanisms are developmentally regulated in the inner cell mass. These results are discussed with regards to apoptosis and the regulation of tissue mass.

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Year:  1991        PMID: 1655543     DOI: 10.1111/j.1432-0436.1991.tb00880.x

Source DB:  PubMed          Journal:  Differentiation        ISSN: 0301-4681            Impact factor:   3.880


  31 in total

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2.  Apoptosis: A New Mechanism of Lethal Myocardial "Reperfusion Injury"?

Authors: 
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3.  Saccharomyces cerevisiae has distinct adaptive responses to both hydrogen peroxide and menadione.

Authors:  D J Jamieson
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

4.  Programmed Cell Death in Plants.

Authors:  R. I. Pennell; C. Lamb
Journal:  Plant Cell       Date:  1997-07       Impact factor: 11.277

5.  In vitro developmental potential of macaque oocytes, derived from unstimulated ovaries, following maturation in the presence of glutathione ethyl ester.

Authors:  E C Curnow; J P Ryan; D M Saunders; E S Hayes
Journal:  Hum Reprod       Date:  2010-08-20       Impact factor: 6.918

6.  PEP-1-frataxin significantly increases cell proliferation and neuroblast differentiation by reducing lipid peroxidation in the mouse dentate gyrus.

Authors:  Woosuk Kim; Dae Won Kim; Bich Na Shin; Dae Young Yoo; Sung Min Nam; Mi Jin Kim; Jung Hoon Choi; Yeo Sung Yoon; Moo-Ho Won; Soo Young Choi; In Koo Hwang
Journal:  Neurochem Res       Date:  2011-09-01       Impact factor: 3.996

Review 7.  Interaction between glutathione and apoptosis in systemic lupus erythematosus.

Authors:  Dilip Shah; Sangita Sah; Swapan K Nath
Journal:  Autoimmun Rev       Date:  2012-12-29       Impact factor: 9.754

8.  Heat stress and antioxidant enzyme activity in bubaline (Bubalus bubalis) oocytes during in vitro maturation.

Authors:  Syma Ashraf Waiz; Mohammad Raies-Ul-Haq; Suman Dhanda; Anil Kumar; T Sridhar Goud; M S Chauhan; R C Upadhyay
Journal:  Int J Biometeorol       Date:  2016-01-19       Impact factor: 3.787

9.  Transgenic mice overexpressing ornithine and S-adenosylmethionine decarboxylases maintain a physiological polyamine homoeostasis in their tissues.

Authors:  R Heljasvaara; I Veress; M Halmekytö; L Alhonen; J Jänne; P Laajala; A Pajunen
Journal:  Biochem J       Date:  1997-04-15       Impact factor: 3.857

10.  Elucidation of the molecular mechanisms of a salicylhydrazide class of compounds by proteomic analysis.

Authors:  Xuefei Cao; Carmen Plasencia; Atsuko Kanzaki; Austin Yang; Terrence R Burke; Nouri Neamati
Journal:  Curr Cancer Drug Targets       Date:  2009-03       Impact factor: 3.428

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