Literature DB >> 2351641

Medium flow rate modulates autocrine-paracrine feedback of GH and PRL release by perifused GH3 cells.

M E Stachura1, C A Lapp, J M Tyler, Y S Lee.   

Abstract

We previously documented both the spontaneous acceleration of growth hormone (GH) and prolactin (PRL) production by GH3 cells during perifusion and the suppression of their production during plate culture. We here present the role played by medium flow itself in this differential behavior. Increasing rates of perifusion flow (pump rates of 1 to 5 ml/h, equivalent to chamber flow rates of 0.19 to 1.3 microliters.min-1.mm-2 of cross-sectional area) were associated with enhanced GH and PRL secretion. Flow rate-dependent basal hormone secretion rates were established quickly and were stable for the first 10 to 14 h of perifusion. The previously documented independent, spontaneous, and continuously accelerating production of both hormones that followed during the subsequent 40 (PRL) to 60 (GH) h of perifusion was also shown to be flow-rate related. Any time the rate of medium flow was changed within an experiment, the rate of hormone secretion was modulated. However, that modulation did not interrupt ongoing flow-associated acceleration of hormone production once the latter had begun. In addition, GH3 cell product(s) from one cell column reversibly inhibited secretion from cells in a downstream column. The inhibition did not occur when cells in the downstream column had been exposed to trypsin. Other work had suggested that neither GH, PRL, insulinlike growth factor-I, leucine, nor nutrient exhaustion were responsible for the effect. These data are consistent with autocrine-paracrine feedback regulation of GH3 cells by a secretory product(s). Feedback would thus provide a mechanism to effect flow-rate-dependent modulation of GH and PRL release, and to explain accelerating hormone production during perifusion.

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Year:  1990        PMID: 2351641     DOI: 10.1007/bf02624090

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  47 in total

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2.  In vitro evidence against the anterior pituitary as a site of negative feedback of prolactin.

Authors:  J L Voogt; W F Ganong
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3.  Modulation of somatostatin binding to rat pituitary membranes by exogenously administered growth hormone.

Authors:  H Katakami; M Berelowitz; M Marbach; L A Frohman
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4.  Superfused pituitary cell cultures: effects of culture conditions on apparent responsiveness to LHRH stimulation administered as short duration pulses.

Authors:  J L O'Conner; A R Clary; T A Kellom
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5.  Continuous perifusion of dispersed anterior pituitary cells: technical aspects.

Authors:  W S Evans; M J Cronin; M O Thorner
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

6.  Sequestration of an early-release pool of growth hormone and prolactin in GH3 rat pituitary tumor.

Authors:  M E Stachura
Journal:  Endocrinology       Date:  1982-12       Impact factor: 4.736

7.  Effects of insulin-like growth factors on adult male rat pituitary function in tissue culture.

Authors:  C G Goodyer; L De Stephano; H J Guyda; B I Posner
Journal:  Endocrinology       Date:  1984-10       Impact factor: 4.736

8.  Physiological concentrations of L-leucine control the release of prolactin from cultured rat pituitary cells.

Authors:  M Cross; A M Walker
Journal:  Endocrinology       Date:  1984-01       Impact factor: 4.736

9.  Human growth hormone and somatomedin C suppress the spontaneous release of growth hormone in unanesthetized rats.

Authors:  H Abe; M E Molitch; J J Van Wyk; L E Underwood
Journal:  Endocrinology       Date:  1983-10       Impact factor: 4.736

10.  GH3 cell secretion of growth hormone and prolactin increases spontaneously during perifusion.

Authors:  C A Lapp; M E Stachura; J M Tyler; Y S Lee
Journal:  In Vitro Cell Dev Biol       Date:  1987-10
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  2 in total

Review 1.  Growth hormone. A paracrine growth factor?

Authors:  S Harvey; K L Hull
Journal:  Endocrine       Date:  1997-12       Impact factor: 3.633

2.  Growth hormone receptor synthesis and release in tumorous somatolactotrophs.

Authors:  K L Hull; E J Sanders; S Harvey
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