1981
DOI: 10.1016/0309-1651(81)90202-2
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A role for lactate in the differentiation of cultured sheep thyroid cells

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1983
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Cited by 10 publications
(3 citation statements)
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“…The inhibiting effect of glucose on differentiation is not restricted to HT-29 cells: primary cultures of chick embryo neuroretinal cells accumulate lens specific 6crystalline when cultured in low glucose but fail to do so if supplementary glucose is added (De Pomerai and Gali, 1982); glucose inhibits the functional differentiation of primary cultures of sheep thyroid cells (Mothersill et al, 1981). Along with the results in HT-29 cells, these data suggest that glucose metabolism is involved in the regulation of cell differentiation.…”
Section: -mentioning
confidence: 59%
“…The inhibiting effect of glucose on differentiation is not restricted to HT-29 cells: primary cultures of chick embryo neuroretinal cells accumulate lens specific 6crystalline when cultured in low glucose but fail to do so if supplementary glucose is added (De Pomerai and Gali, 1982); glucose inhibits the functional differentiation of primary cultures of sheep thyroid cells (Mothersill et al, 1981). Along with the results in HT-29 cells, these data suggest that glucose metabolism is involved in the regulation of cell differentiation.…”
Section: -mentioning
confidence: 59%
“…The level of differentiation obtainable is high, follicular development, T, production and iodine trapping being detectable [ 70, 721. Differentiation is dependent on thyrotropic hormone and on availability of lactate which is used in the process of follicle formation [73]. Absence of these substances leads to dedifferentiation and growth of cells.…”
Section: Development Of New Transformation Systemsmentioning
confidence: 99%
“…The follicular morphology im¬ proved for up to 20 days after which the cells rapidly died due to lack of nutrients (Mothersill et al 1980). Differentiated cell life could be extended up to 30 days by using conditioned medium from 10-15 day cultures for medium changes after day 20 and further extension of the differentiated life span to cultures could be produced by adding concentrated glucose solutions (5 mg in 0.1 ml medium per flask) to the medium just before the cell death was due to occur (Mothersill et al 1981). …”
mentioning
confidence: 99%