Literature DB >> 3742717

The induction of transformed-like morphology and enhanced growth in Syrian hamster embryo cells grown at acidic pH.

R A LeBoeuf, G A Kerckaert.   

Abstract

The effect of the pH, Na+ concentration and osmolality of the culture medium on early passage Syrian hamster embryo (SHE) clonal cell proliferation was examined. The pH of the medium was adjusted from 6.49 to 7.45 by addition of different amounts of NaHCO3 to the medium and incubating the cell cultures in a fixed atmosphere of 10% CO2/90% air. Our results indicate that clonal SHE cell proliferation is optimal at pH 6.65-6.80 while plating efficiency is independent of pH between 6.65 and 7.45. Adjustment of Na+ to that concentration in the medium (3450 p.p.m., 0.15 M) of the greatest NaHCO3 addition caused a moderate depression of cell proliferation over the entire pH series. Adjusting the osmolality of the culture medium to a constant value of 338 mOsm/kg did not alter the pH effect on cell proliferation. The pH of the medium also affected cellular and colony morphology. Below pH 6.90 there was an increase in the number of colonies which exhibited a transformed-like morphology ('altered' colonies). The 'altered' phenotype was characterized by a multilayered, criss-cross pattern of growth throughout the colony. This phenotype was stable upon sub-cloning into pH 6.65 medium but was reversible if sub-cloned into pH 7.36 medium. The induction of 'altered' colonies at low pH could be partially suppressed by Na+ or osmolality adjustment. These results are discussed in terms of optimizing growth conditions for SHE cells in order to enhance their usefulness for cell transformation studies. The induction of 'altered' colonies by low pH is also discussed relative to the involvement of pH regulation in tumor-promoter and growth-factor action on cells in culture.

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Year:  1986        PMID: 3742717     DOI: 10.1093/carcin/7.9.1431

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  8 in total

1.  Phenotypic differences between Syrian hamster embryo cells cultured at pH 6.7 or 7.3.

Authors:  R J Isfort; D B Cody; T N Asquith; R A LeBoeuf
Journal:  In Vitro Cell Dev Biol       Date:  1992 Sep-Oct

2.  Effects of media buffer systems on growth and electrophysiologic characteristics of cultured sweat duct cells.

Authors:  C L Bell; P M Quinton
Journal:  In Vitro Cell Dev Biol       Date:  1991-01

3.  A novel mechanism of acid and bile acid-induced DNA damage involving Na+/H+ exchanger: implication for Barrett's oesophagus.

Authors:  Aaron Goldman; Mohammad Shahidullah; David Goldman; Ludmila Khailova; George Watts; Nicholas Delamere; Katerina Dvorak
Journal:  Gut       Date:  2010-09-28       Impact factor: 23.059

4.  Acidic pH induces topoisomerase II-mediated DNA damage.

Authors:  Hai Xiao; Tsai-Kun Li; Jin-Ming Yang; Leroy F Liu
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-11       Impact factor: 11.205

5.  Pantoprazole Induces Apoptosis of Leukemic Cells by Inhibiting Expression of P-Glycoprotein/Multidrug Resistance-Associated Protein-1 Through PI3K/AKT/mTOR Signaling.

Authors:  Miao Liu; Rong Tang; Yi Jiang
Journal:  Indian J Hematol Blood Transfus       Date:  2017-03-30       Impact factor: 0.900

6.  Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs.

Authors:  Stuart Creton; Marilyn J Aardema; Paul L Carmichael; James S Harvey; Francis L Martin; Robert F Newbold; Michael R O'Donovan; Kamala Pant; Albrecht Poth; Ayako Sakai; Kiyoshi Sasaki; Andrew D Scott; Leonard M Schechtman; Rhine R Shen; Noriho Tanaka; Hemad Yasaei
Journal:  Mutagenesis       Date:  2011-08-17       Impact factor: 3.000

7.  A biologically based model of growth and senescence of Syrian hamster embryo (SHE) cells after exposure to arsenic.

Authors:  K H Liao; D L Gustafson; M H Fox; L S Chubb; K F Reardon; R S Yang
Journal:  Environ Health Perspect       Date:  2001-12       Impact factor: 9.031

8.  Improvement of the BALB/c-3T3 cell transformation assay: a tool for investigating cancer mechanisms and therapies.

Authors:  Doerte Poburski; René Thierbach
Journal:  Sci Rep       Date:  2016-09-09       Impact factor: 4.379

  8 in total

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