Expression of glucocorticoid receptor beta in lymphocytes of patients withglucocorticoid-resistant ulcerative colitis

Citation
M. Honda et al., Expression of glucocorticoid receptor beta in lymphocytes of patients withglucocorticoid-resistant ulcerative colitis, GASTROENTY, 118(5), 2000, pp. 859-866
Citations number
30
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
GASTROENTEROLOGY
ISSN journal
00165085 → ACNP
Volume
118
Issue
5
Year of publication
2000
Pages
859 - 866
Database
ISI
SICI code
0016-5085(200005)118:5<859:EOGRBI>2.0.ZU;2-I
Abstract
Background & Aims. Recently, the glucocorticoid receptor beta (hGR beta) wa s suggested to play a role as a dominant negative regulator for determining glucocorticoid response. The aim of this study was to clarify whether reve rse-transcription polymerase chain reaction (RT-PCR) analysis of hGR beta m essenger RNA (mRNA) can predict the response to glucocorticoids in patients with ulcerative colitis. Methods: Total RNA obtained from peripheral blood mononuclear cells (PBMCs) of 23 patients with ulcerative colitis and 20 he althy volunteers was reverse transcribed; the resulting complementary DNA w as amplified using specific primers for hGR alpha and hGR beta. Protein exp ression of hGR in PBMCs was confirmed by immunoprecipitation-Western blot a nalysis. Results: The expression of hGR alpha mRNA (477 base pairs) was det ected in all patients and all healthy volunteers, In contrast, a hGR beta m RNA (366 base pairs) was detected in 1 (9.1%) of 11 glucocorticoid-sensitiv e patients, 10 (83.3%) of 12 glucocorticoid-resistant patients, and 2 (10%) of 20 healthy volunteers. The positive rate of hGR beta mRNA in the resist ant group was significantly higher than that in the sensitive group (P = 0. 0019). The hGR beta band could be detected by immunoprecipitation-Western b lotting in hGR beta mRNA-positive patients. Conclusions: The results show t hat the expression of hGR beta mRNA in PBMCs examined by RT-PCR may serve a s a novel predictor of glucocorticoid response in ulcerative colitis.