Expression of glucocorticoid receptor β in lymphocytes of patients with glucocorticoid-resistant ulcerative colitis
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Honda, M
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Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, JapanAsahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, Japan
Honda, M
[1
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Orii, F
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Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, JapanAsahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, Japan
Orii, F
[1
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Ayabe, T
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Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, JapanAsahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, Japan
Ayabe, T
[1
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Imai, S
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Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, JapanAsahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, Japan
Imai, S
[1
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Ashida, T
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Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, JapanAsahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, Japan
Ashida, T
[1
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Obara, T
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Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, JapanAsahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, Japan
Obara, T
[1
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Kohgo, Y
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Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, JapanAsahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, Japan
Kohgo, Y
[1
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机构:
[1] Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, Japan
Background & Aims. Recently, the glucocorticoid receptor beta (hGR beta) was suggested to play a role as a dominant negative regulator for determining glucocorticoid response. The aim of this study was to clarify whether reverse-transcription polymerase chain reaction (RT-PCR) analysis of hGR beta messenger 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 healthy volunteers was reverse transcribed; the resulting complementary DNA was amplified using specific primers for hGR alpha and hGR beta. Protein expression of hGR in PBMCs was confirmed by immunoprecipitation-Western blot analysis. Results: The expression of hGR alpha mRNA (477 base pairs) was detected in all patients and all healthy volunteers, In contrast, a hGR beta mRNA (366 base pairs) was detected in 1 (9.1%) of 11 glucocorticoid-sensitive 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 resistant group was significantly higher than that in the sensitive group (P = 0.0019). The hGR beta band could be detected by immunoprecipitation-Western blotting in hGR beta mRNA-positive patients. Conclusions: The results show that the expression of hGR beta mRNA in PBMCs examined by RT-PCR may serve as a novel predictor of glucocorticoid response in ulcerative colitis.
机构:
UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
AUPHAN, N
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DIDONATO, JA
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
DIDONATO, JA
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ROSETTE, C
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
ROSETTE, C
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HELMBERG, A
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
HELMBERG, A
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KARIN, M
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
机构:
UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
AUPHAN, N
;
DIDONATO, JA
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
DIDONATO, JA
;
ROSETTE, C
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
ROSETTE, C
;
HELMBERG, A
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
HELMBERG, A
;
KARIN, M
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA