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  • 1
    ISSN: 1432-2307
    Keywords: Immunohistochemistry ; Electron microscopy ; ACTH ; Pituitary gland ; Neoplasm
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Immunohistochemical localization of theN-terminal fragment (1–76) (NTF) of human pro-opiomelanocortin (POMC) was studied in human adult and fetal pituitary glands, as well as in pituitary adenomas associated with Cushing's syndrome and in ectopic ACTH-producing tumors. Comparison of localization between NTF and ACTH was performed using mirror sections. Our results indicated concomitant localization of NTF and ACTH in the same cells, not only in normal adult and fetal pituitaries but also in pituitary adenomas and ectopic ACTH producing tumours. Specificity of the NTF staining was confirmed by immunoabsorption. Negative staining of the bovine pituitary gland indicated the immunohistochemical localization ofN-terminal (1–45) of human POMC as there is a known species difference in the sequence 1–45 between human and the bovineN-terminal fragment. Presence of NTF in cisterna of rough endoplasmic reticulum indicates its production by small cell carcinoma. These findings, together with the previous studies, suggest that the complete form of POMC is produced in the tumours as well as in normal pituitaries.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-198X
    Keywords: ANGiotensinogen ; Gene expression ; Human growth hormone fusion gene ; Steroids ; Thyroid hormone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract To identify tissue- and hormonal-specific DNA controlcis-elements in the rat gene, we have constructed fusion genes consisting of various lengths of the 5′-flanking region of the rat angiotensinogen gene linked to a human growth hormone (hGH) reporter gene and have introduced them into a subclone of rat pancreatic islet tumor cell line (1056A) which expresses the highest level of angiotensinogen mRNA. As a negative control, we have also introduced them into a human choriocarcinoma cell line (JEG-3), which does not express the endogenous angiotensinogen gene. The level of the expression of these fusion genes in these cells was determined by the level of immunoreactive hGH secreted into the culture medium. The expression of angiotensinogen-growth hormone (ANG-GH) fusion genes, pOGH (ANG N-1498/+18), pOGH (ANG N-688/+18), pOGH (ANG N-110/+18), pOGH (ANG N-53/+18), and pOGH (ANG N-35/+18) was 1.0, 1.8, 1.5, 12.0 and 3.0-fold higher, respectively, than the promoterless growth hormone expression vector (pOGH). The addition of dexamethasone (10−6 M), aldosterone (10−5 M), and thyroid hormone, L-T3 (10−7 M), stimulated the expression of pOGH (ANG N-1498/+18) by 4.0-, 2.5-, and 2.0-fold above the control level, respectively. Combination of dexamethasone (10−6 M), L-T3 (10−7 M), and ethinyl-estradiol (10−6 M) stimulated the expression of the pOGH (ANG N-1498/+18) to greater than 10-fold over the control. Ethinyl-estradiol (10−6 M) or progesterone (10−6 M) alone had no effect on the expression of the pOGH (ANG N-1498/+18). These studies demonstrate that the induction of expression of the angiotensinogen gene by dexamethasone and L-T3 in 1056A cells is due to a transcriptional mechanism and the 1056A cells could be useful for studying angiotensinogen gene regulation and for identifying the glucocorticoid and L-T3-responsivecis-regulatory elements in the angiotensinogen gene.
    Type of Medium: Electronic Resource
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