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Characterization of nuclear thyroid hormone receptors of cultured skin fibroblasts from patients with resistance to thyroid hormone.

作者信息

Ichikawa K, Hughes I A, Horwitz A L, DeGroot L J

出版信息

Metabolism. 1987 Apr;36(4):392-9. doi: 10.1016/0026-0495(87)90214-9.

DOI:10.1016/0026-0495(87)90214-9
PMID:3561254
Abstract

Nuclear thyroid hormone receptors of patients with the syndrome of resistance to thyroid hormone were investigated in cell lines from seven patients in four affected families and compared to results from six normals. Fibroblasts cultured from skin biopsies were used. When binding affinity and capacity for L-triiodothyronine (T3) were examined by incubating whole cells or isolated nuclei, no significant differences were found. The amount of receptor released during the incubation of nuclei (9.3% to 19.0% of total nuclear receptors) was also within the normal range in these patients. When T3 binding assays were performed on 0.3 mol/L KCl extracted receptor, a significant decrease in binding capacity (MBC) without a difference in binding affinity (Ka) was observed in four patients and a lower Ka with normal MBC was found in two patients. Recovery of receptors in saline extracts, from patients' fibroblasts showing a low MBC, was low in comparison to normals. Lability of salt extracted receptors at 38 degrees C was normal and salt extractability of T3 occupied receptors, examined by incubation of [125I]-T3 labeled nuclei with various concentrations of KCl, was only slightly decreased. This lower salt extractability of receptors was insufficient to account for the low MBC obtained by Scatchard analysis of T3 binding to nuclear extracts. Gel filtration and density gradient sedimentation of salt-extracted receptors showed Stokes radius of 34 A, and sedimentation coefficient of 3.4 S in all patients and normals. From these values, molecular weight of 49,000 and total frictional ratio (f/fo) of 1.4 were calculated for nuclear receptors from patients and normals, suggesting a somewhat asymmetrical shape of receptors.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

相似文献

1
Characterization of nuclear thyroid hormone receptors of cultured skin fibroblasts from patients with resistance to thyroid hormone.
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2
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引用本文的文献

1
Characterization of a thyroid hormone receptor expressed in human kidney and other tissues.人肾及其他组织中表达的甲状腺激素受体的特性分析。
Proc Natl Acad Sci U S A. 1988 Apr;85(8):2781-5. doi: 10.1073/pnas.85.8.2781.
2
The molecular basis of thyroid hormone action.甲状腺激素作用的分子基础。
J Endocrinol Invest. 1989 Dec;12(11):843-61. doi: 10.1007/BF03350080.
3
Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor beta.与人类甲状腺激素受体β配体结合域突变相关的全身性甲状腺激素抵抗。
Proc Natl Acad Sci U S A. 1989 Nov;86(22):8977-81. doi: 10.1073/pnas.86.22.8977.
4
A base mutation of the C-erbA beta thyroid hormone receptor in a kindred with generalized thyroid hormone resistance. Molecular heterogeneity in two other kindreds.一个患有全身性甲状腺激素抵抗的家族中C-erbAβ甲状腺激素受体的碱基突变。另外两个家族中的分子异质性。
J Clin Invest. 1990 Jan;85(1):93-100. doi: 10.1172/JCI114438.
5
Thyroid hormone resistance syndrome. Inhibition of normal receptor function by mutant thyroid hormone receptors.甲状腺激素抵抗综合征。突变型甲状腺激素受体对正常受体功能的抑制。
J Clin Invest. 1991 Jun;87(6):1977-84. doi: 10.1172/JCI115225.
6
Screening of nineteen unrelated families with generalized resistance to thyroid hormone for known point mutations in the thyroid hormone receptor beta gene and the detection of a new mutation.对19个甲状腺激素全身性抵抗的无关家族进行甲状腺激素受体β基因已知点突变的筛查及一个新突变的检测。
J Clin Invest. 1991 Feb;87(2):496-502. doi: 10.1172/JCI115023.
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Tight linkage of the human c-erbA beta gene with the syndrome of generalized thyroid hormone resistance is present in multiple kindreds.人类c-erbAβ基因与全身性甲状腺激素抵抗综合征紧密连锁,在多个家族中均有发现。
J Endocrinol Invest. 1991 Mar;14(3):219-23. doi: 10.1007/BF03346792.
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Generalized thyroid hormone resistance: identification of an arginine to cystine mutation in codon 315 of the c-erb A beta thyroid hormone receptor.全身性甲状腺激素抵抗:c-erb Aβ甲状腺激素受体第315密码子精氨酸至胱氨酸突变的鉴定
J Endocrinol Invest. 1992 Sep;15(8):573-9. doi: 10.1007/BF03344927.