help button home button Endocrine Society Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tagami, T.
Right arrow Articles by Imura, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tagami, T.
Right arrow Articles by Imura, H.

Endocrinology, Vol 127, 1727-1734, Copyright © 1990 by Endocrine Society


ARTICLES

Immunohistochemical localization of nuclear 3,5,3'-triiodothyronine receptor proteins in rat tissues studied with antiserum against C-ERB A/T3 receptor

T Tagami, H Nakamura, S Sasaki, T Mori, H Yoshioka, H Yoshida and H Imura
Department of Internal Medicine, Kyoto University School of Medicine, Japan.

We have previously raised an anti-c-erb A peptide antibody (designated 4B II) which immunoprecipitated in vitro transcription/translation products of c-erb A alpha 1 and beta. 4B II could recognize nuclear T3 receptor (NT3R) without distinction between difference in species and tissues. Using 4B II, we studied immunohistochemical localization of NT3R proteins in various tissues of the rat. Cryostat sections (4-6 microns) of selected rat tissues were incubated with 4B II at 4C overnight, followed by fluorescein-isothyocianate-conjugated anti- rabbit immunoglobulin G for 60 min at 25 C. The cellular localization of fluorescence in all tissues examined was exclusively nuclear. Under the same conditions, control sections stained with antiserum which had previously absorbed with c-erb A peptide or inactive serum showed no specific staining. In the brain the large nuclei, supposed to be neuronal, were strongly stained in the cerebral cortex and the granular layer of the cerebellum. In the kidney, cells in the glomerulus, the distal, but not the proximal, tubules, and the collecting ducts exhibited nuclear staining. Nuclear fluorescence was observed homogeneously in the heart and liver, but the intensity was much weaker in the latter. Less intense fluorescence was seen in the testis and spleen, although specific immunostaining was clearly observed in the nuclei of spermatocytes, Leydig cells, and the heads of the sperms in the testis, and many lymphocytes in the spleen. Nuclei of follicular cells of the thyroid exhibited very strong fluorescence, suggesting existence of plenty of NT3R proteins. The anterior pituitary showed strong immunostaining in most nuclei, and clear nuclear fluorescence was also detected in the intermediate lobe of the pituitary. The present study showed that NT3R distributes selectively in certain types of cells in many tissues and that the content of NT3R proteins seems to correlate with the concentration of c-erb A mRNA alpha 1 and beta among many organs.


This article has been cited by other articles:


Home page
J. Clin. Endocrinol. Metab.Home page
K. Moriyama, T. Tagami, T. Usui, M. Naruse, T. Nambu, Y. Hataya, N. Kanamoto, Y.-s. Li, A. Yasoda, H. Arai, et al.
Antithyroid Drugs Inhibit Thyroid Hormone Receptor-Mediated Transcription
J. Clin. Endocrinol. Metab., March 1, 2007; 92(3): 1066 - 1072.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
B. Zandieh Doulabi, M. Platvoet-ter Schiphorst, H. C. van Beeren, W. T. Labruyere, W. H. Lamers, E. Fliers, O. Bakker, and W. M. Wiersinga
TR{beta}1 Protein Is Preferentially Expressed in the Pericentral Zone of Rat Liver and Exhibits Marked Diurnal Variation
Endocrinology, March 1, 2002; 143(3): 979 - 984.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
F. A. R. Neves, R. R. Cavalieri, L. A. Simeoni, D. G. Gardner, J. D. Baxter, B. F. Scharschmidt, N. Lomri, and R. C. J. Ribeiro
Thyroid Hormone Export Varies among Primary Cells and Appears to Differ from Hormone Uptake
Endocrinology, February 1, 2002; 143(2): 476 - 483.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
H.B. S. Ariyaratne, N. Mills, J. I. Mason, and S.M.L. C. Mendis-Handagama
Effects of Thyroid Hormone on Leydig Cell Regeneration in the Adult Rat Following Ethane Dimethane Sulphonate Treatment
Biol Reprod, October 1, 2000; 63(4): 1115 - 1123.
[Abstract] [Full Text]


Home page
Biol. Reprod.Home page
J. J. Buzzard, J. R. Morrison, M. K. O'Bryan, Q. Song, and N. G. Wreford
Developmental Expression of Thyroid Hormone Receptors in the Rat Testis
Biol Reprod, March 1, 2000; 62(3): 664 - 669.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
P. R. Manna, M. Tena-Sempere, and I. T. Huhtaniemi
Molecular Mechanisms of Thyroid Hormone-stimulated Steroidogenesis in Mouse Leydig Tumor Cells. INVOLVEMENT OF THE STEROIDOGENIC ACUTE REGULATORY () PROTEIN
J. Biol. Chem., February 26, 1999; 274(9): 5909 - 5918.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
SuzanneB. Brown, M. Maloney, and WilliamB. Kinlaw
"Spot 14" Protein Functions at the Pretranslational Level in the Regulation of Hepatic Metabolism by Thyroid Hormone and Glucose
J. Biol. Chem., January 24, 1997; 272(4): 2163 - 2166.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1990 by The Endocrine Society