1960
DOI: 10.1016/0014-4827(60)90117-8
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Studies on properties of surfaces required for growth of mammalian cells in synthetic medium

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Cited by 102 publications
(18 citation statements)
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“…Paramoeba was often seen in large clumps in such areas. Similar observations have been recorded for other cell types(24). Divalent cations were not required for adhesion ofParamoeba to polystyrene surfaces, as amoebae adhered well in CMF alone.…”
supporting
confidence: 87%
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“…Paramoeba was often seen in large clumps in such areas. Similar observations have been recorded for other cell types(24). Divalent cations were not required for adhesion ofParamoeba to polystyrene surfaces, as amoebae adhered well in CMF alone.…”
supporting
confidence: 87%
“…Once sufficient contact between cell and substrate has occurred, charge density exerts little effect on Paramoeba, as morphology and locomotive rates in each medium do not differ between treated and untreated dishes or culture tubes. In the case of glass substrata, sodium ions, which are complexed with SiO-residues, are ionized when in contact with liquid media; hence, the greater the soda (Na,O) content of glass, the greater the negative surface charge density of the glass (24). Thus, if negative charge density were strictly dependent on substrate composition, slides and cover slips should give a low percent transmission (i.e.…”
Section: Discussionmentioning
confidence: 99%
“…The idea that sterilization may affect cell adhesion by causing changes in the glass surface has been introduced in 1965, 12 based on observations of poor fibroblast attachment to Pyrex glass pre-treated with NaOH. 13 Still, there is no clear understanding of the specific changes in glass surfaces introduced by alkali, acid or water-steam treatment, and of heating and sterilizing procedures in general. A clear correlation between adhesion strength of mammalian cells and the nanoroughness of glass following sterilization treatment has also not been established so far.…”
Section: Discussionmentioning
confidence: 99%
“…Since HeLa cells were first established in vitro as a strain readily grown by serial subculture (1, 2) they have been exceptionally widely used for the propagation of viruses and for a variety of other purposes such, for example, as the study of cell adherence (3,4) and mitosis (5), the assay of toxic substances (6), and the investigation of biosynthetic processes (7). However, despite the ubiquity of HeLa ceils in many types of laboratory, relatively little has been reported concerning their fine structure under normal conditions of culture, the electron microscope having mainly been used to study them after infection with various viruses (8)(9)(10)(11)(12)(13).…”
Section: Introductionmentioning
confidence: 99%