scholarly journals Dynamics of proopiomelanocortin and prohormone convertase 2 gene expression in Xenopus melanotrope cells during long-term background adaptation

1998 ◽  
Vol 159 (2) ◽  
pp. 281-286 ◽  
Author(s):  
CH Dotman ◽  
F van Herp ◽  
GJ Martens ◽  
BG Jenks ◽  
EW Roubos

The toad Xenopus laevis is able to adapt its skin color to background light intensity. In this neuroendocrine reflex, the proopiomelanocortin (POMC)-derived peptide alpha-melanophore-stimulating hormone (alphaMSH) is a key regulatory factor. In animals adapting to a black background, release of alphaMSH from the pituitary pars intermedia causes dispersal of melanin in skin melanophores. To investigate the long-term in vivo dynamics of alphaMSH production during black background adaptation, the biosynthetic rate of POMC and the contents of POMC, alphaMSH and the POMC processing enzyme precursor convertase 2 (PC2) have been studied in the pars intermedia using pulse-labeling, Western blot and radioimmunoassay. In control animals, adapted to a white background, the rate of POMC biosynthesis and the POMC content were low, while high alphaMSH and PC2 contents were found. After 1 week of adaptation to a black background, the rate of POMC biosynthesis and the POMC protein content had increased 19- and 3.7-fold respectively. These parameters attained a maximum level (28- and 5. 8-fold higher than control) after 3 weeks and remained at these elevated levels for at least 12 weeks. After 1 week, the pars intermedia content of alphaMSH was only 30% of the control level, but after 6 and 12 weeks, the alphaMSH level had increased to the control level. The PC2 content decreased to 52% of control after 1 week and stabilized after 3 weeks at a level slightly lower than the control value. The results show that during long-term background adaptation a steady-state situation is reached, with a balance between the biosynthesis, enzymatic processing and release of alphaMSH. The in vivo dynamics of the processing enzyme PC2 suggest a parallel storage and release of alphaMSH and mature PC2 in the Xenopus pituitary pars intermedia.

1977 ◽  
Vol 55 (6) ◽  
pp. 922-927 ◽  
Author(s):  
B. G. Jenks ◽  
A. P. VanOverbeeke ◽  
B. F. McStay

Pituitary levels of melanophore-stimulating hormone (MSH), release of MSH, and protein synthetic activity in the pars intermedia were determined in Xenopus laevis during background adaptation. MSH was measured using a radioimmunoassay to α-MSH; uptake of [3H]lysine, determined autoradiographically, was used to assess protein synthesis; changes in melanophore index indicated changes in release of MSH. Adaptation to black background led to eventual depletion of MSH and increased protein synthetic activity. Conversely, during adaptation to a white background MSH levels increased and protein synthesis decreased. Changes in synthesis lagged considerably behind changes in release. During the initial stage of black-background adaptation, release of MSH was not accompanied by simultaneous decrease in levels of MSH in the gland from which it is concluded that replenishment of MSH took place. Our results indicated that this replenishment in the gland could not be accounted for by de novo synthesis of the hormone. It is proposed that a stored precursor to MSH exists, conversion of which provides for rapid replenishment of MSH. It is suggested that the factor(s) controlling MSH release affect synthesis of this hormone only indirectly.


1992 ◽  
Vol 135 (3) ◽  
pp. 469-478 ◽  
Author(s):  
K. Maruthainar ◽  
Y. Peng-Loh ◽  
D. G. Smyth

ABSTRACT β-Endorphin-and α-melanotrophin (α-MSH)-related peptides were extracted from the pars intermedia of Xenopus laevis maintained for 2, 4 or 6 weeks on a white background and for the same periods on a black background. The peptides were resolved under dissociating conditions by gel exclusion chromatography on Sephadex G-50 and they were detected by radioimmunoassay with antibodies to β-endorphin, α,N-acetyl β-endorphin and α-MSH. The β-endorphin-related peptides separated into two fractions of different molecular size. Further purification of the peptides in each fraction was by ion exchange chromatography on SP-Sephadex C-25 and by high-pressure liquid chromatography. The α-MSH-related peptides were resolved by gel exclusion and ion exchange chromatography. The purified β-endorphin- and α-MSH-immunoreactive peptides were identified by comparison of their chromatographic properties with the corresponding peptides from porcine pituitary or by comparison with synthetic peptides. The major form of β-endorphin in the pars intermedia of the frog adapted to a white background was identified as α,N-acetyl β-endorphin (1–8); it was accompanied by a small quantity of acetylated peptides with molecular size similar to β-endorphin. In contrast, the pars intermedia of the frogs adapted to a black background contained approximately equal amounts of α,N-acetyl β-endorphin (1–8) and the larger forms of β-endorphin. The higher molecular weight forms were identified as the α,N-acetyl derivatives of β-endorphin (1–26), (1–27) and (1–31); however after 6 weeks of white adaptation the sole remaining peptide in this group was the 26-residue peptide. An additional β-endorphin immunoreactive peptide, provisionally identified as β-endorphin (10–26), was present in both black- and white-adapted animals; the amounts of this peptide increased during white adaptation. Major differences in the processing of α-MSH were also observed. In the frogs adapted to a black background des-acetyl α-MSH greatly predominated over the acetyl form whereas after 6- weeks adaptation to a white background the acetylated peptide proved to be the principal component. The results demonstrate that the proteolytic processing of β-endorphin and the acetylation of α-MSH in Xenopus laevis are influenced by background adaptation. The formation of β-endorphin (1–8) appears to reflect the action of an endopeptidase that acts at the single arginine residue present at position 9. This cleavage does not appear to take place in mammalian β-endorphins where position 9 is occupied by lysine. Journal of Endocrinology (1992) 135, 469–478


In a previous contribution (Hogben and Slome, 1931) evidence was brought forward to show that the white background response does not depend on the same mechanism of coordination as the black background response, which is produced by reflex liberation of a hormone (“B” substance) of the pars intermedia in the pituitary gland; and experiments pointing to the existence of another internal secretion (“W” substance), connected directly or indirectly with the activity of the pars tuberalis, were described. The existence of separate receptor components of the retina controlling the two systems was left for subsequent enquiry. Of two possible hypotheses concerning the nature of the receptive mechanism, the most likely one is illustrated diagrammatically in fig. 1. In normal situations, when an animal is illuminated on a black background, light can only fall on the floor of the retina. If it is aquatic, the maximum divergence of any two rays which strike the eye is twice the critical angle for air and water, so that in the absence of reflexion of rays from sur­rounding objects below the surface of separation all rays will presumably be brought to a sharp focus in shallow water. There are thus three distinct possibilities which arise from the way in which the animal is illuminated if, as in Xenopus , the eyes are situated on the top of the head: ( a ) in darkness no part of the retina is stimulated, the same being true of the eyeless animal; ( b ) when the animal is exposed to a black background only a sharply localized region of the retina is stimulated; ( c ) when the animal is exposed to a white background the whole of the retina is illuminated owing to the scattering of rays in all directions from the surroundings. For convenience of description the usual black back­ground situation will be described hereafter as one in which only the “floor” of the retina is stimulated, and the white background situation as one in which the floor and the “ periphery ” of the retina are both stimulated together. If then, the receptor elements of the floor and periphery initiate different systems of reflex arcs the phenomena of the background response in Amphibia and Reptiles may be interpreted as follows. In Reptiles we may suppose that stimulation of floor reflexly excites the melanophores to expand, while stimulation of peripheral photoreceptors excites them to contract, being presumably prepotent in the final common path. In Amphibia two alternatives may be con­sidered: ( a ) that floor elements reflexly excite liberation of “B” and that peripheral photoreceptors, being prepotent, reflexly inhibit libera­tion of “B"; ( b ) that floor elements reflexly excite liberation of “B”, and peripheral photoreceptors reflexly excite production of the antago­nistic substance “W” in quantity sufficient to over-ride the effect of “B”. The crucial test of the truth of the general hypothesis that the floor and peripheral elements of the retina initiate different processes of coordina­tion was suggested by Keeble and Gamble (1904-6) in their experiments on Crustacea. If it is true, a normal animal illuminated from below in a black tank with a white top should react in exactly the same way as a normal animal when illuminated in a black tank from above. On the other hand, a normal animal illuminated from below in a black tank with a black top should react like an eyeless animal in the same situation, because the floor elements would not be subject to stimulation. The experiment may be varied as indicated below. In order to obtain signi­ficant results two classes of precautions must be carefully observed. One is that the physical dimensions of the tank must not exceed certain limits, since the maximal divergence of two rays is rigidly fixed when an animal is illuminated from above. The other is that there must be no air-water interface to permit reflexion of the incident rays downwards. Aside from the fact that no bubbles must be allowed to collect, this condition presents a practical difficulty if the animal has to come to the surface to breathe.


Blood ◽  
1997 ◽  
Vol 89 (5) ◽  
pp. 1551-1559 ◽  
Author(s):  
Wen Zhou ◽  
Christopher F. Toombs ◽  
Tong Zou ◽  
Jane Guo ◽  
Murray O. Robinson

Abstract The consequences of long-term in vivo expression of human c-mpl ligand in a mouse model were examined. Transgenic mice expressing the human full-length cDNA in the liver exhibited a fourfold increase in circulating platelet count that persisted stably over the life of the animals. Transgenic animals thrived and appeared healthy for at least 500 days. Transgenic platelets appeared normal with respect to surface antigens and response to platelet aggregation agonists. The highest-expressing transgenic line maintained human c-mpl ligand serum levels of 3 ng/mL. Megakaryocyte numbers in bone marrow and spleen were elevated, as were bone marrow and spleen megakaryocyte colony-forming cells (MEG-CFC). Megakaryocytes were observed in the bone marrow, spleen, liver, and lung, but in no other sites. Circulating myeloid and lymphoid cell populations were increased twofold. Additionally, the animals had a slight but significant anemia despite an increase in marrow colony-forming units-erythroid (CFU-E). No evidence of myelofibrosis was observed in the bone marrow. The platelet nadir in response to administration of either antiplatelet serum (APS) or 5-fluorouracil (5FU) was significantly reduced relative to the control level. Furthermore, the red blood cell (RBC) nadir was reduced relative to control levels in both models, suggesting that c-mpl ligand can directly or indirectly support the maintenance of erythrocyte levels following thrombopoietic insult.


1995 ◽  
Vol 146 (1) ◽  
pp. 159-167 ◽  
Author(s):  
F J C van Strien ◽  
L Galas ◽  
B G Jenks ◽  
E W Roubos

Abstract Immunocytochemical analysis revealed the presence of acetylated endorphins in both melanotropes and corticotropes of the pituitary gland of Xenopus laevis. Chemical acetylation studies to determine the steady-state level of acetylated versus non-acetylated endorphins showed that virtually all endorphins are acetylated in both melanotropes and corticotropes. Apparently Xenopus is unique among vertebrates as non-acetylated endorphins are major endproducts in the distal lobe of all other vertebrate species studied thus far. The dynamics of endorphin biosynthesis in melanotrope cells using pulse-chase analysis coupled to immunoaffinity chromatography revealed that processing of pro-opiomelanocortin to produce N-terminalacetylated endorphins is very rapid. To determine the effect of long-term background adaptation on acetylation status of endorphins and α-MSH-related peptides, Xenopus laevis were adapted for 3 or 6 weeks to either a black or a white background. In both physiological states the major intracellular form of α-MSH-related peptides in melanotropes was desacetyl α-MSH while the major endorphin-related peptide was α,N-acetyl-β-endorphin[1–8]. In the medium of superfused neurointermediate lobes of black background-adapted animals the major form of secreted melanotropins and endorphins was α-MSH and α,N-acetyl-β-endorphin[1–8] respectively. We conclude that there is a marked spatio-temporal difference in acetylation of melanotropin and endorphins, with rapid intracellular acetylation of endorphins while melanotropin is acetylated at the time of its exocytosis. In the medium of superfused neurointermediate lobes of white background-adapted animals the amount of desacetyl α-MSH was much higher than in the medium of lobes of black-adapted animals. Therefore, the secretory signals from melanotrope cells of black- and white-adapted Xenopus appear to differ with respect to the degree of acetylation of the melanotropins. This difference may underlie the strategy of Xenopus to regulate dermal melanophore activity during physiological background adaptations. Journal of Endocrinology (1995) 146, 159–167


1972 ◽  
Vol 53 (2) ◽  
pp. 303-NP ◽  
Author(s):  
B. WEATHERHEAD ◽  
P. WHUR

SUMMARY The fact that the transfer of amphibians between black and white backgrounds causes the 'melanocyte-stimulating hormone (MSH) cells' of the pars intermedia of the pituitary to undergo considerable morphological change has been established for some time. The application of morphometric techniques to the 'MSH cells' of Xenopus has permitted the quantitative analysis of these changes at the ultrastructural level. Of the nine classes of organelle selected for analysis in these cells, three, namely nucleus, plasma membrane and dense bodies, showed no statistically significant changes. The remaining classes of organelle all showed significant changes in the percentage of the total cell volume that they occupied, although not all the organelles changed at the same rate. Transfer of animals from a white to a black background for up to 12 days was associated with increase in the percent volume of rough endoplasmic reticulum, Golgi membranes, Golgi granules and mitochondria and with a decrease in the percent volume of the fibrous granules. Return of animals to a white background after 6 days on a black background produced a reversal of the above changes with return to, or close to, white background (control) levels. This quantitative ultrastructural approach also highlights discrepancies in both the rate and magnitude of the changes in some of the organelles and related non-morphological parameters previously reported, e.g. the size of the rough endoplasmic reticulum and the rate of incorporation of labelled amino acid into protein; or the numbers of fibrous granules and the levels of detectable pituitary MSH. Some possible interpretations of these discrepancies are discussed.


Blood ◽  
1997 ◽  
Vol 89 (5) ◽  
pp. 1551-1559 ◽  
Author(s):  
Wen Zhou ◽  
Christopher F. Toombs ◽  
Tong Zou ◽  
Jane Guo ◽  
Murray O. Robinson

The consequences of long-term in vivo expression of human c-mpl ligand in a mouse model were examined. Transgenic mice expressing the human full-length cDNA in the liver exhibited a fourfold increase in circulating platelet count that persisted stably over the life of the animals. Transgenic animals thrived and appeared healthy for at least 500 days. Transgenic platelets appeared normal with respect to surface antigens and response to platelet aggregation agonists. The highest-expressing transgenic line maintained human c-mpl ligand serum levels of 3 ng/mL. Megakaryocyte numbers in bone marrow and spleen were elevated, as were bone marrow and spleen megakaryocyte colony-forming cells (MEG-CFC). Megakaryocytes were observed in the bone marrow, spleen, liver, and lung, but in no other sites. Circulating myeloid and lymphoid cell populations were increased twofold. Additionally, the animals had a slight but significant anemia despite an increase in marrow colony-forming units-erythroid (CFU-E). No evidence of myelofibrosis was observed in the bone marrow. The platelet nadir in response to administration of either antiplatelet serum (APS) or 5-fluorouracil (5FU) was significantly reduced relative to the control level. Furthermore, the red blood cell (RBC) nadir was reduced relative to control levels in both models, suggesting that c-mpl ligand can directly or indirectly support the maintenance of erythrocyte levels following thrombopoietic insult.


1971 ◽  
Vol 51 (3) ◽  
pp. 521-532 ◽  
Author(s):  
P. WHUR ◽  
B. WEATHERHEAD

SUMMARY Xenopus were kept on, and transferred between, black or white back-grounds before incubating the pars intermedia and sometimes other parts of the pituitary with [3H]leucine. The rates of incorporation of label were assessed either by liquid scintillation counting of trichloroacetic acid precipitates or quantitative analysis of autoradiographs. Inhibition of incorporation of label was achieved after incubation with puromycin, showing that the label was associated with newly synthesized peptide material. The rates of incorporation of label into pars distalis and pars nervosa were not significantly different in animals from black or white back-grounds. However, pars intermedia from animals on a black background incorporated label at three to six times the rate of animals from a white background. In animals kept for some days on a white background and then transferred to a black background the rate of incorporation began to rise within a few minutes and reached the new higher level after several hours. In animals transferred from a black to a white background, however, no decline in rate was detected until 2 days after the transfer, but by 3 days the rate had returned to the white background level. The timing of these changes bears no relationship to the timing of changes, reported elsewhere, in the ultrastructure of pars intermedia cells after changes in background colour. They are, on the other hand, similar to the timing of changes in the melanocyte-stimulating hormone content of pars intermedia and also to changes in the melanophore index.


1984 ◽  
Vol 101 (3) ◽  
pp. 277-284 ◽  
Author(s):  
K. T. Rodrigues ◽  
J. P. Sumpter

ABSTRACT Radioimmunoassays for α-MSH, β-MSH, ACTH and endorphin were used to measure pituitary concentrations of these peptides in rainbow trout during adaptation to black and white backgrounds. There was no difference in the pituitary content of any of these peptides between long-term black- and white-adapted trout. Plasma levels of α-MSH immunoreactivity were significantly higher in black-adapted trout than in white-adapted trout. Time-course studies revealed that although the body colour of trout showed an initial rapid adaptation to background colour, this was not paralleled by a corresponding change in plasma α-MSH levels. These only showed significant changes after 7 or more days of background adaptation, when melanophore recruitment or degradation occurred on black or white backgrounds respectively. Intravenous administration of mammalian α-MSH, salmon β-MSH I or antibodies to these peptides did not affect short-term background adaptation. However, long-term administration of mammalian α-MSH via osmotic minipump maintained melanophore numbers in grey-adapted trout transferred to a white background, although this observation was based on only two fish. It is concluded that peptides derived from pro-opiomelanocortin do not appear to be involved in controlling physiological colour change but may be involved in regulating morphological colour change of the rainbow trout. J. Endocr. (1984) 101, 277–284


2014 ◽  
Vol 62 (S 01) ◽  
Author(s):  
M. Sigler ◽  
S. Huell ◽  
R. Foth ◽  
W. Ruschewski ◽  
T. Tirilomis ◽  
...  

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