scholarly journals Differential distribution of S-100 protein and vimentin in the hypophyseal pars tuberalis of the guinea pig.

1996 ◽  
Vol 44 (5) ◽  
pp. 501-510 ◽  
Author(s):  
Y Kameda

In the hypophyseal pars tuberalis of guinea pigs, I examined immunohistochemical localization and development of vimentin and S-100 protein in comparison with those of the pars distalis. In the pars distalis, almost all folliculostellate cells expressed intense immunoreactivity for vimentin. A subpopulation of vimentin-immunoreactive folliculostellate cells was also immunoreactive for S-100 protein. During fetal development, vimentin-immunoreactive cells appeared at mid-gestation in the pars distalis and became numerous at late stages, whereas only a few S-100 immunoreactive cells were observed even at late stages. In the pars tuberalis, a large number of vimentin-immunoreactive cells were distributed in the cranial region surrounding the median eminence and the dorsocaudal region surrounding the infundibular stalk. These cells, however, were sparse in the ventrocaudal region in continuity with the pars distalis. Conversely, dense distribution of S-100 immunoreactive cells was restricted in the ventrocaudal region. Vimentin-immunoreactive cells were elongated and were mostly distributed as solitary cells, whereas S-100 immunoreactive cells were gathered in large or small cell groups and frequently formed colloid-containing follicles. During fetal development, large cell groups immunoreactive for S-100 protein were detected at late stages in the ventrocaudal region. Therefore, in the pars tuberalis S-100 immunoreactive cells are distinct from the vimentin cells and do not correspond to the folliculostellate cells of the pars distalis.

1986 ◽  
Vol 10 (10) ◽  
pp. 765-773 ◽  
Author(s):  
F MICHETTI ◽  
M RENDE ◽  
L LAURIOLA ◽  
V STOLFI ◽  
G CALOGERO ◽  
...  

1965 ◽  
Vol 31 (3) ◽  
pp. 279-287 ◽  
Author(s):  
B. A. YOUNG ◽  
C. L. FOSTER ◽  
E. CAMERON

SUMMARY The ultrastructure of the adenohypophysis of the rabbit is described preliminary to reporting changes after experimental procedures. Fixation by perfusing with gluteraldehyde enabled selected regions of the gland to be removed with accuracy. Separate descriptions of the pars distalis proper, zona tuberalis, pars tuberalis and pars intermedia are therefore included. In the pars distalis proper four types of granular cell were recognized although their function cannot be accurately determined. For convenience, therefore, they have been designated 1, 2, 3 and 4. In addition a fifth type of cell (type 5) is described which is also present in the other areas. This cell, as well as having possible phagocytic functions, appears to be concerned in the formation of a perivascular channel. Two types of cell are recognized in the zona tuberalis, which are similar in appearance to the 3 and 4 cells of the pars distalis, although not necessarily identical in function. The characteristic cells of the pars tuberalis are rich in cytoplasmic RNA and contain large numbers of intracellular fibrils. It is suggested that the ribosomes are concerned in the synthesis of a sedentary protein which may take the form of the microfibrils. The pars intermedia contains a predominant cell type with large granules of varying density. The relationship of these granules to the specific hormone is discussed.


1993 ◽  
Vol 41 (2) ◽  
pp. 307-311 ◽  
Author(s):  
M J Olson ◽  
J L Martin ◽  
A C LaRosa ◽  
A N Brady ◽  
L R Pohl

The enzymatic esterase activity of carboxylesterases is integral to the nasal toxicity of many esters used as industrial solvents or in polymer manufacture, including propylene glycol monomethyl ether acetate, dimethyl glutarate, dimethyl succinate, dimethyl adipate, and ethyl acrylate. Inhalation of these chemicals specifically damages the olfactory mucosa of rodents. We report the localization and differential distribution of a 59 KD carboxylesterase in nasal tissues of the rat by immunohistochemistry. Rabbit antiserum against the 59 KD rat liver microsomal carboxylesterase bound most prominently to the olfactory mucosa when applied to decalcified, paraffin-embedded sections of rat nasal turbinates. Within the olfactory mucosa, anti-carboxylesterase did not bind to sensory neurons, the target cell for ester-initiated toxicity; these cells apparently lack carboxylesterase. Instead, the antibody was preferentially bound by cells of Bowman's glands and sustentacular epithelial cells which are immediately adjacent to the olfactory nerve cells. In contrast, non-olfactory tissues (respiratory mucosa and squamous epithelium), which are more resistant to the toxicity of esters, had less carboxylesterase content. The distribution of immunoreactivity correlated well with the distribution of carboxylesterase catalytic activity described elsewhere. These findings help to link the metabolic fate of inhaled esters to the site-specific pathological findings that follow exposure to such chemicals.


1989 ◽  
Vol 12 (11) ◽  
pp. 929-935 ◽  
Author(s):  
Kimiya Sugimura ◽  
Hajime Haimoto ◽  
Hiroshi Nagura ◽  
Kanefusa Kato ◽  
Akira Takahashi

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