Literature DB >> 6619197

Phosphatidylethanolamine synthesis in ethanolamine-responsive and -nonresponsive cells in culture.

T Kano-Sueoka, J E Errick, D King, L A Walsh.   

Abstract

Mammalian cells can be classified into two types based upon whether or not they show growth response to ethanolamine (Etn) in culture. The content of phosphatidylethanolamine (PE) in phospholipid and incorporation of radioactive Etn into the cells were examined in the Etn-responsive and -nonresponsive cells in order to elucidate the mechanisms of growth stimulation by Etn. In all Etn-responsive cells tested, 5 microM Etn significantly altered the composition of cellular phospholipid compared to that grown without Etn, while Etn-nonresponsive cells had a similar phospholipid composition whether the growth medium contained Etn or not. Using two rat mammary carcinoma cell lines, 64-24 (responsive type) and 22-1 (nonresponsive type), further studies were carried out. In 64-24 cells there was a proportional increase in PE content as the dosage of Etn in the medium was increased. The increase in PE content leveled off at 10 microM. Further, the increase in PE content was correlated with increased rate of growth. In contrast, PE content or growth rate did not change at all in 22-1 cells. In 64-24 cells radioactive Etn (0.1-50 microM) was incorporated four- to five-fold more efficiently into phospholipid, and the aqueous pool of precursors of PE was ten times less as compared to 22-1 cells, indicating that Etn-responsive cells utilize Etn supplied in the medium to synthesize PE far more efficiently than Etn-nonresponsive cells. De novo synthesis of PE must not be sufficient to support optimum growth in Etn-responsive cells.

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Year:  1983        PMID: 6619197     DOI: 10.1002/jcp.1041170115

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  6 in total

1.  Ethanolamine enhances the proliferation of intestinal epithelial cells via the mTOR signaling pathway and mitochondrial function.

Authors:  Huansheng Yang; Xia Xiong; Tiejun Li; Yulong Yin
Journal:  In Vitro Cell Dev Biol Anim       Date:  2016-03-22       Impact factor: 2.416

2.  Insufficiency of transformation by simian virus 40, polyomavirus, EJ-ras, or v-myc oncogenes for conversion of ethanolamine-responsive mammary cells to ethanolamine-nonresponsive cells.

Authors:  T Kano-Sueoka; D M King
Journal:  J Virol       Date:  1988-09       Impact factor: 5.103

3.  Phosphatidylethanolamine deficiency in membrane lipids inhibits keratinocyte intercellular networks formation.

Authors:  T Kano-Sueoka; D Oda; J K Kawamoto
Journal:  In Vitro Cell Dev Biol Anim       Date:  2001 Nov-Dec       Impact factor: 2.416

4.  Ethanolamine modulates DNA synthesis through epidermal growth factor receptor in rat primary hepatocytes.

Authors:  Hisae Kume; Hajime Sasaki
Journal:  In Vitro Cell Dev Biol Anim       Date:  2006 Jan-Feb       Impact factor: 2.416

5.  Evidence for an ethanolamine cycle: differential recycling of the ethanolamine moiety of phosphatidylethanolamine derived from phosphatidylserine and ethanolamine.

Authors:  Y J Shiao; J E Vance
Journal:  Biochem J       Date:  1995-09-01       Impact factor: 3.857

6.  Analysis of cytosolic phosphoethanolamine and ethanolamine and their correlation with prognostic factors in breast cancer.

Authors:  T Kano-Sueoka; T Watanabe; T Miya; H Kasai
Journal:  Jpn J Cancer Res       Date:  1991-07
  6 in total

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