Journal Article
Research Support, Non-U.S. Gov't
Add like
Add dislike
Add to saved papers

Simultaneous localization of Pit-1 protein and gonadotropins on the same cell type in the anterior pituitary glands of the rat.

Pit-1 is a prototypic member of the POU transcription factor family and plays a critical role in pituitary-specific action of growth hormone (GH), prolactin (PRL), and thyroid-stimulating hormone (TSH) beta-subunit genes. The purpose of the present study was to elucidate the changes in the expression of the Pit-1 product in the pituitary of pregnant rats employing an improved double-immunohistochemical method. The positive cells showed nuclear immunoreactivity and Pit-1 protein was frequently observed in the nuclei of many cells which were also immunopositive for GH, PRL, and betaTSH. Unexpectedly, a significant number of pituitary cells containing both Pit-1 and gonadotropins were also observed. These cells were usually distributed near blood vessels that supply the pituitary. While a prominent increase in the percentage of Pit-1/PRL, Pit-1/beta-luteinizing hormone and Pit-1/beta-follicle-stimulating hormone immunoreactive cells was observed in pregnant rats, the percentage of Pit-1/GH immunoreactive cells was strongly decreased. In contrast, no significant differences in the percentage of Pit-1/betaTSH doubly immunolabeled cells were noticed. Our findings strongly support the hypothesis that PRL could coexist in the Pit-1 immunopositive gonadotropes. Although Pit-1 protein was not detected in the nuclei of corticotropes, the existence of these cells in the rat pituitary cannot be excluded.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app