IMMUNOHISTOCHEMICAL STUDY OF THE HUMAN PITUITARY WITH ANTI-LUTEINIZING HORMONE, ANTI-FOLLICLE STIMULATING HORMONE AND ANTI-THYROTROPHIN SERA

1973 ◽  
Vol 72 (4) ◽  
pp. 625-642 ◽  
Author(s):  
C. Robyn ◽  
P. Leleux ◽  
L. Vanhaelst ◽  
J. Golstein ◽  
M. Herlant ◽  
...  

ABSTRACT Sections of fixed human pituitaries were investigated by an indirect immunofluorescence technique using antisera obtained following immunization of rabbits with human chorionic gonadotrophin (HCG), human hypophyseal gonadotrophins (HHG) and bovine hypophyseal thyrotrophin (BTSH) preparations. After microphotography of immunofluorescent positive cells, the tissue sections were stained by the Alcian blue (or Thionine aldehyde)-Periodic Acid Schiff-Orange G method. The microscopical fields which had been examined in immunofluorescence were then relocated and photographed again. A correlation was established between the cells reacting with an antiserum and the cell types of the morphological nomenclatures for human adenohypophysis proposed by Romeis (1940) and by Pearse & van Noorden (1963) and those of the functional classification proposed by Herlant & Pasteels (1967). The specificity of the antisera was checked by immunoelectrophoresis and by neutralization of the biological activities of luteinizing hormone (LH), follicle stimulating hormone (FSH) and BTSH. After selective absorption of the FSH neutralizing antibodies an anti-HCG serum became specific for LH. After selective absorption of the LH neutralizing antibodies an anti-HHG serum was found specific for FSH. The anti-BTSH sera neutralized the biological activity of human TSH, but cross reacted in immunoelectrophoresis with ovine LH and in immunofluorescence with the gonadotrophic cells of human pituitaries. After absorption with HCG, an anti-BTSH serum produced a specific immunofluorescence in large purple blue to dark blue Romeis δ cells filled with fine Alcian blue (or Thionine aldehyde) positive granules. This cell type is equivalent to the S2 mucoids of Pearse or to the "Thyrotrophs" of Herlant. The anti-LH and anti-FSH sera cross-reacted with TSH. Indeed, the S2 mucoids were also fluorescence positive with both anti-gonadotrophic sera. In addition, both anti-LH and anti-FSH sera produced a specific immunofluorescence in the group of purple coloured Romeis δ cells closely related to the S1 mucoids of Pearse. This would indicate that the same cell type contains immunoreactive LH and FSH, which is in contradiction with the description of two different gonadotrophic cell types based on histochemical stainings of human and animal pituitaries obtained in various physiopathological conditions.

1997 ◽  
Vol 45 (6) ◽  
pp. 785-794 ◽  
Author(s):  
Jennifer Armstrong ◽  
Gwen V. Childs

C-fos expression appears in some activated cell types. Because of dynamic changes in gonadotropes during the estrous cycle, this study was initiated to determine if fos might be expressed in gonadotropes before any period of activation. We detected c-fos and pituitary antigens in dissociated anterior pituitary cells by dual-labeling immunocy-tochemistry. The highest percentages of cells with fos protein were found in proestrous rat populations. In diestrous and proestrous populations, dual labeling showed that 6–9% of pituitary cells contained fos with adrenocorticotropin, thyroid-stimulating hormone, prolactin, or growth hormone antigens. In contrast, only 0.8–3% contained fos with luteinizing hormone (LH) or follicle-stimulating hormone (FSH) antigens. We then tested the hypothesis that gonadotropes might increase fos expression earlier in the cycle. In populations from metestrous rats, c-fos labeling was found in 45% of LH cells compared to only 23% of LH cells in the proestrous group. This suggests that proportionately more LH cells are being activated to produce fos early in the cycle. Perhaps fos is used in translation of LHβ antigens or gonadotropin-releasing hormone (GnRH) receptor mRNAs. In contrast, less than 1% of all pituitary cells expressed fos with FSH at all stages of the cycle (only 6–12% of FSH cells). This differential expression suggests one mechanism behind the regulation of non-parallel storage and release of gonadotropin antigens.


Aquaculture ◽  
2008 ◽  
Vol 274 (2-4) ◽  
pp. 408-415 ◽  
Author(s):  
Youichi Hayakawa ◽  
Tetsuro Morita ◽  
Wataru Kitamura ◽  
Shinji Kanda ◽  
Akira Banba ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document