Ciba Foundation Symposium 81 - Peptides of the Pars

Content:
Chapter 1 Chairman's advent (pages 1–2): G.M. Besser
Chapter 2 The Intermediate Lobe of the Pituitary Gland: advent and historical past (pages 3–12): Aaron B. Lerner
Chapter three constitution and Chemistry of the Peptide Hormones of the Intermediate Lobe (pages 13–31): Alex N. Eberle
Chapter four comparability of Rat Anterior and Intermediate Pituitary in Tissue tradition: Corticotropin (ACTH) and ??Endorphin (pages 32–54): Richard E. Mains and Betty A. Eipper
Chapter five Processing, Turnover and unlock of Corticotropins, Endorphins and Melanotropin within the Toad Pituitary Intermediate Lobe (pages 55–78): Y. Peng Loh
Chapter 6 ??Endorphin?Related Peptides within the Pituitary Gland: Isolation, id and Distribution (pages 79–100): D. G. Smyth, S. Zakarian, J. F. W. Deakin and D. E. Massey
Chapter 7 wonderful constitution and Cytochemistry of the Mammalian Pars Intermedia (pages 101–127): M. E. Stoeckel, G. Schmitt and A. Porte
Chapter eight Distribution, Subcellular Localization and identification of Immunoreactive ??Melanotropin within the Pituitary Gland and mind (pages 128–140): I. C. Porter, F. J. H. Tilders, A. Barnea and C. R. Parker
Chapter nine Nature and keep an eye on of Peptide liberate from the Pars Intermedia (pages 141–165): Sue Jackson, J. desire, F. Estivariz and P. J. Lowry
Chapter 10 organic position of the Pars Intermedia in reduce Vertebrates (pages 166–179): Bridget I. Baker
Chapter eleven The Pars Intermedia and the Fetal Pituitary?Adrenal Axis (pages 180–195): R.E. Silman, Cathy road, Diane Holland, T. Chard, J. Falconer and J. S. Robinson
Chapter 12 services of ??Melanotropin and different Opiomelanocortin Peptides in Labour, Intrauterine progress and mind improvement (pages 196–223): D. F. Swaab and J. T. Martin
Chapter thirteen Pars Intermedia Peptides: experiences in grownup people (pages 224–243): Sally J. Ratter, Lorraine McLoughlin, Glenda Gillies, Vicky Clement?Jones, J. desire and Lesley H. Rees
Chapter 14 organic activities of Melanocyte?Stimulating Hormone (pages 244–262): Mac E. Hadley, Christopher B. Heward, Victor I. Hruby, Tomi ok. Sawyer and younger C. S. Yang
Chapter 15 ? ?Melanotropin and mind functionality (pages 263–276): Jan M. Van Ree, Bela Bohus, Katharina M. Csontos, Willem Hendrik Gispen, Henk M. Greven, Frans P. Nijkamp, Fred A. Opmeer, Guus (A.) A. De Rotte, Tjeerd B. Van Wimersma Greidanus, Albert Witter and David De Wed
Chapter sixteen Melanocyte?Stimulating Hormone and Adaptive Behaviour (pages 277–294): Tjeerd B. Van Wimersma Greidanus, Guus (A.) A. De Rotte, Anthony J. Thody and Alex N. Eberle
Chapter 17 Chairman's final feedback (pages 299–300): G.M. Besser

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Immunostaining was blocked by addition of the appropriate synthetic peptide. Background cells may arise in part from posterior lobe pituicytes. The number of cells in the cultures increased greatly with time in culture; the rate of incorporation of labelled amino acid into TCA- (trichloroacetic acid) precipitable material increased 18-fold in 9 days. 38 MAINS AND EIPPER FIG. 2. Phase-contrast micrographs of intermediate-posterior pituitary cultures. Tenday-old cultures of intermediate-posterior pituitary cells, maintained in XDMEMCO, and 5% rat serum,were photographed in the live state.

REFERENCES Eberle A, Schwyzer R 1975 Hormone-receptor interactions. Helv Chim Acta 58:1528-1535 Eberle A, Schwyzer R 1976 Hormone-receptor interactions. The message sequence of amelanotropin: demonstration of two active sites. Helv Chim Acta 622452-2459 Eberle A, Schwyzer R 1979b Multiply labelled or-MSH derivatives for degradation studies. Experientia (Basel) 35: 961 CHEMISTRY OF INTERMEDIATE LOBE PEPTIDES 31 Sawyer TK, Sanfilippo RJ, Hruby VJ, Engle MH, Heward CB, Burnett JB, Hadley ME 1980 [Nle4, D-Phe' ] -a-melanocyte stimulating hormone: a highly potent or-melanotropin with ultralong biological activity.

Conditions were developed for the stable, long-term tissue culture of dissociated intermediate-posterior pituitary cells. Extracts of cells maintained in tissue culture for 18 h or nine days had the same content of immunoreactivep-endorphin, 16K fragment, ACTH(18-39) (or CLIP) and ACTH(17-24). Throughout the nine days in culture, characteristic cells that could be immunostained with antibodies to various regions of proACTH/endorphin were present; during the time in culture, non-reactive background cells multiplied rapidly.

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