1975
DOI: 10.1530/acta.0.0790217
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Organ Culture of Human Somatotrophic Pituitary Adenomas: Ultrastructure and Growth Hormone Production

Abstract: Ten somatotrophic adenomas removed from acromegalic patients and fragments of the non-tumoural surrounding pituitary were submitted to organ culture for periods of up to one month. Electron microscopic observation shows that these tumours retain their histological differentiation throughout the culture period. The cell morphology of the cultured tumours remains essentially unchanged and in particular the secretory granules keep their initial size (150 and 130 nm). However the granules disappear gradually so th… Show more

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Cited by 16 publications
(4 citation statements)
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“…Many investigators have cultured pituitary ade nomas. ', 3,4,8,9,11,12,14,17) We previously reported 6) that monolayer cultures of GH-producing pituitary ade nomas exhibit many degenerative changes in the absence of any drug. Therefore, monolayer cultures are not suitable for investigating morphological changes.…”
Section: Resultsmentioning
confidence: 99%
“…Many investigators have cultured pituitary ade nomas. ', 3,4,8,9,11,12,14,17) We previously reported 6) that monolayer cultures of GH-producing pituitary ade nomas exhibit many degenerative changes in the absence of any drug. Therefore, monolayer cultures are not suitable for investigating morphological changes.…”
Section: Resultsmentioning
confidence: 99%
“…However, most other investigators such as Betzdorf et al (1971), Peillon et al (1975) and Kageyama et al (1976) reported the duration of GH secretion to be 2-4 weeks. Minute amounts of GH secretion have been reported by Kageyama et al (1976) in some tumors from nonacromegalic patients, but the amount seemed to be too small to describe to tumoral secretions.…”
Section: Discussionmentioning
confidence: 96%
“…1969;Peillon et al 1975Peillon et al , 1976) the present study was undertaken in order 1) to determine whether in the same culture system PRL secretion and synthesis might occur in these tumours with or without in vivo PRL hypersécrétion 2) to compare the rate and evolution of PRL and GH secretion and synthesis by the same tumours and 3) in addition to evaluate the effect of somatostatin (GHIF) upon PRL secretion from these tumours in short-term incubation.…”
mentioning
confidence: 99%