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Heterogeneous dopamine D2 receptor subtype messenger ribonucleic acid expression in clinically nonfunctioning
U Renner1, T Arzberger, U Pagotto
1Max-Planck-Institute of Psychiatry, Clinical Institute, Department of Endocrinology, Munich, Germany. renner@mpipsykl.mpg.de
The Journal of Clinical Endocrinology and Metabolism
|April 29, 1998
Summary
Dopamine D2 receptor (D2R) subtypes, D2short and D2long, show varied expression in nonfunctioning pituitary adenomas. This heterogeneity may impact bromocriptine
Area of Science:
- Endocrinology
- Molecular Biology
- Neuroscience
Background:
- Dopamine D2 receptor (D2R) subtypes, D2short (D2s) and D2long (D2l), play crucial roles in pituitary function.
- Limited understanding exists regarding D2R subtype expression and function in normal and adenomatous pituitary tissues.
Purpose of the Study:
- To investigate the messenger RNA (mRNA) expression of D2R subtypes in clinically nonfunctioning pituitary adenomas.
- To explore the localization and functional implications of D2R subtype expression in these tumors.
Main Methods:
- In situ hybridization using subtype-specific oligonucleotides to analyze D2R mRNA expression.
- Immunohistochemistry to determine D2R localization within adenoma cells.
- In vitro cell culture to assess the effect of bromocriptine on tumor cell proliferation.
Main Results:
- Normal pituitaries exhibit a predominant D2l isoform expression.
- Nonfunctioning pituitary adenomas display heterogeneous D2R subtype expression, with some lacking D2R mRNA entirely.
- D2R was primarily localized in gonadotropin-immunopositive cells (LH and FSH) within adenomas.
- Bromocriptine's growth inhibitory effect was observed in only a subset of adenoma cultures, potentially linked to D2R subtype expression.
Conclusions:
- Clinically nonfunctioning pituitary adenomas show diverse D2R subtype expression patterns, differing from normal pituitary tissue.
- The heterogeneous D2R expression may explain the variable response to bromocriptine therapy.
- Further research is needed to confirm the role of the D2s subtype in mediating bromocriptine's growth inhibitory effects.