The distribution of immunoreactive α-melanocyte-stimulating hormone cells in the adult human pituitary gland

1986 ◽  
Vol 111 (2) ◽  
pp. 335-NP ◽  
Author(s):  
P. J. Coates ◽  
I. Doniach ◽  
A. C. Hale ◽  
L. H. Rees

ABSTRACT It has been suggested that a proportion of the adenomas and the nodular hyperplasia of cells in the pituitary gland in cases of Cushing's disease are derived from cells of the pars intermedia rather than the pars anterior. The evidence can be summarized as follows: (1) the posterior site of adenoma or nodular hyperplasia in the pituitary, (2) the innervation of cells and (3) the suppressive response to the dopamine agonist bromocriptine in vivo or to dopamine in vitro. All these observations infer analogy with cells of the pars intermedia of other species, which are controlled by direct neural tonic dopaminergic inhibition. The adult human pituitary gland, however, does not possess a morphologically distinct pars intermedia, due to regression of the rudimentary fetal pars intermedia after birth, with mixing of cells into the pars anterior and pars nervosa. Since cells of the pars intermedia characteristically synthesize α-MSH, we have studied this peptide in order to assess the occurrence and distribution of intermedia-derived cells in the adult human pituitary. Sections from 100 pituitaries, removed at autopsy, were stained by an indirect immunoperoxidase technique using non-cross-reacting antisera specific for α-MSH and ACTH. Immunoreactive α-MSH (IR-α-MSH) cells were found in a total of 97 specimens. Of these, only ten cases showed a marked concentration of IR-α-MSH cells in the zona intermedia. In the majority of pituitaries, IR-α-MSH cells were more commonly seen in the pars anterior than in the zona intermedia; in 41 cases, IR-α-MSH cells were completely absent from the zona intermedia. The number of IR-α-MSH cells varied greatly, from less than ten cells per section to many hundreds, regardless of the age or sex of the individual. Additionally, no correlation could be made between the number of IR-α-MSH cells and the cause of death, treatment or the period of time between death and removal of the pituitary. We conclude that cells containing IR-α-MSH are present in varying numbers in the normal adult human pituitary gland. These cells do not show a specific distribution pattern, but may be found in both the zona intermedia and are spread throughout the pars anterior. J. Endocr. (1986) 111, 335–342

1989 ◽  
Vol 120 (3) ◽  
pp. 525-NP ◽  
Author(s):  
P. J. Coates ◽  
I. Doniach ◽  
J. M. P. Holly ◽  
L. H. Rees

ABSTRACT Immunocytochemistry, radioimmunoassay and high-performance liquid chromatography (HPLC) techniques have been used in combination to investigate the presence of immunoreactive (ir)-α-MSH in the normal human pituitary gland, and to investigate the possible origin of these cells from the fetal pars intermedia. Two separate antisera to α-MSH were employed in immunocytochemistry to distinguish between authentic α-MSH and the desacetyl form. Only desacetyl α-MSH was detected in the pituitary gland of fetal and adult man, in both the pars (zona) intermedia and the pars anterior. In the fetus, a large proportion of the ACTH-containing cells of the anterior lobe also contained ir-α-MSH, while ir-α-MSH containing cells were more sparse in adults. Radioimmunoassay of acid extracts of adult pituitary tissue showed α-MSH levels representing less than 0·05% of the ACTH content of the gland. HPLC analysis of these extracts confirmed that only the desacetyl form was present. These results suggest that α-MSH peptides are synthesized by anterior lobe cells of the human pituitary gland, which are not derived from the fetal pars intermedia. Possible regulatory mechanisms affecting cells which contain ir-α-MSH are discussed, and by comparison with the intermediate lobe of other species it is concluded that there is little evidence for a true intermediate lobe in the human pituitary gland. Journal of Endocrinology (1989) 120, 525–530


Author(s):  
Eva Horvath ◽  
Kalman Kovacs

The human pituitary gland consists of two major components: the adenohypophysis comprising the hormone producing cells of the pars anterior, pars intermedia, and pars tuberalis, and the neurohypophysis, also called pars nervosa or posterior lobe (1). In contrast to most mammalian species, the human gland has no anatomically distinct pars intermedia (2). The exclusively proopiomelanocortin (POMC)-producing cells of the pars intermedia are sandwiched between the anterior and posterior lobes in the majority of mammals, whereas in the human they are incorporated within the pars anterior, thereby constituting the pars distalis (3). The pars tuberalis is a minor upward extension of the adenohypophysis attached to the exterior of the lower pituitary stalk. In this chapter we deal only with adenohypophyseal tumours. Histologically, the adenohypophysis consists of a central median (or mucoid) wedge flanked by the two lateral wings. The hormone-producing cell types are distributed in an uneven, but characteristic manner. The cells are arranged within evenly sized acini surrounded by a delicate but well-defined reticulin fibre network giving the pituitary its distinct architecture (4). In the center of the acini is the long-neglected pituitary follicle composed of the agranular nonendocrine folliculo-stellate cells (5).


1983 ◽  
Vol 104 (2) ◽  
pp. 164-166 ◽  
Author(s):  
Akira Miyake ◽  
Keiichi Tasaka ◽  
Shintaro Mori ◽  
Youichi Saito ◽  
Toshihiro Aono

Abstract. The effect of prostaglandin D2 on the release of luteinizing hormone was studied in a superfusion system by superfusing human pituitary gland. Perfusion with 30 μg of prostaglandin D2 induced a significant increase of luteinizing hormone secretion. This is the first evidence of a direct effect of prostaglandin D2 on the secretion of luteinizing hormone from the human pituitary gland. This finding suggests the possible role of prostaglandin D2 in human reproductive function


1983 ◽  
Vol 96 (2) ◽  
pp. 303-309 ◽  
Author(s):  
A. M. McNicol ◽  
H. Thomson ◽  
C. J. R. Stewart

The distribution of specifically stained corticotrophic cells has been studied in the pituitary glands of 11 dogs with pituitary-dependent hyperadrenocorticism. The results suggest that the disease is not a single entity, and that some cases are caused by primary abnormality of the pituitary gland whereas others appear to be the result of dysfunction of the hypothalamus or central nervous system. The patterns correspond closely to those demonstrated in the human pituitary gland in Cushing's disease, and confirm that the canine disease is a useful model for the study of the pathogenesis of the variants of the condition.


1975 ◽  
Vol 379 (1) ◽  
pp. 247-261 ◽  
Author(s):  
Paul Roos ◽  
D.V. Dervartanian ◽  
Gunilla Jacobson ◽  
Leif Wide

1992 ◽  
Vol 56 (5) ◽  
pp. 729-734 ◽  
Author(s):  
Solange C. Hearn ◽  
Philip M. Jones ◽  
Mohammad A. Ghatei ◽  
Johanna Byrne ◽  
Sarah F. Hill ◽  
...  

1985 ◽  
Vol 40 (5) ◽  
pp. 419-422 ◽  
Author(s):  
Errol B. De Souza ◽  
Marilyn H. Perrin ◽  
Peter J. Whitehouse ◽  
Jean Rivier ◽  
Wylie Vale ◽  
...  

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