Korean J Physiol Pharmacol.
1998 Feb;2(1):101-108.
Discrepancy between in vitro and in vivo effect of Galphas gene
mutation on the mRNA expression of TRH receptor
- Affiliations
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- 1Department of Pharmacology, Kyunghee University, College of Medicine, Seoul 130-701, Korea.
- 2Division of Endocrinology, Kyunghee University College of Medicine, Seoul 130-701, Korea.
- 3Department of Internal Medicine, Kyunghee University College of Medicine, Seoul 130-701, Korea.
- 4Institute of Genetic Engineering at Kyunghee University, Seoul 130-701, Korea.
Abstract
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We investigated the effect of alpha-subunit of the stimulatory
GTP-binding protein (Galphas) gene mutation on the expression of the
thyrotropin-releasing hormone (TRH) receptor (TRH-R) gene in GH3 cells
and in growth hormone (GH)-secreting adenomas of acromegalic patients.
In the presence of cycloheximide, forskolin and isobutylmethylxanthine,
cholera toxin, and GH-releasing hormone (GBRH) decreased rat TRH-R
(rTRH-R) gene expression by about 39%, 43.7%, and 46.7%, respectively.
Transient expression of a vector expressing mutant-type Galphas
decreased the rTRH-R gene expression by about 50% at 24 h of
transfection, whereas a wild-type Galphas expression vector did not.
The transcript of human TRH-R (hTRH-R) gene was detected in 6 of 8
(75%) tumors. Three of them (50%) showed the paradoxical GH response to
TRH and the other three patients did not show the response. The
relative expression of hTRH-R mRNA in the tumors from patients with the
paradoxical response of GH to TRH did not differ from that in the
tumors from patients without the paradoxical response. Direct PCR
sequencing of GALPHAs gene disclosed a mutant allele and a normal
allele only at codon 201 in 4 of 8 tumors. The paradoxical response to
TRH was observed in 2 of 4 patients without the mutation, and 2 of 4
patients with the mutation. The hTRH-R gene expression of pituitary
adenomas did not differ between the tumors without the mutation and
those with mutation. The present study suggests that the expression of
TRH-R gene is not likely to be a main determinant for the paradoxical
response of GH to TRH, and that Galphas mutation may suppress the gene
expression of TRH-R in GH-secreting adenoma. However, a certain
predisposing factor(s) may play an important role in determining the
expression of TRH-R.