Linked Life Data

16709608

Source:http://linkedlifedata.com/resource/pubmed/id/16709608

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2006-8-16
pubmed:abstractText
Mutations of the X-linked thyroid hormone (TH) transporter (monocarboxylate transporter, MCT8) produce in humans unusual abnormalities of thyroid function characterized by high serum T3 and low T4 and rT3. The mechanism of these changes remains obscure and raises questions regarding the regulation of intracellular availability and metabolism of TH. To study the pathophysiology of MCT8 deficiency, we generated Mct8 knockout mice. Male mice deficient in Mct8 (Mct8(-/y)) replicate the thyroid abnormalities observed in affected men. TH deprivation and replacement with L-T3 showed that suppression of TSH required higher serum levels T3 in Mct8(-/y) than wild-type (WT) littermates, indicating hypothalamus and/or thyrotroph resistance to T3. Furthermore, T4 is required to maintain the high serum T3 level because the latter was not different between the two genotypes during administration of T3. Mct8(-/y) mice have 2.3-fold higher T3 content in liver associated with 6.1- and 3.1-fold increase in deiodinase 1 mRNA and enzymatic activity, respectively. The relative T3 excess in liver of Mct8(-/y) mice produced a decrease in serum cholesterol (79 +/- 18 vs. 137 +/- 38 mg/dl in WT) and an increase in alkaline phosphatase (107 +/- 23 vs. 58 +/- 3 U/liter in WT) levels. In contrast, T3 content in cerebrum was 1.8-fold lower in Mct8(-/y) mice, associated with a 1.6- and 10.6-fold increase in D2 mRNA and enzymatic activity, respectively, as previously observed in TH-deprived WT mice. We conclude that cell-specific differences in intracellular TH content due to differences in contribution of the various TH transporters are responsible for the unusual clinical presentation of this defect, in contrast to TH deficiency.
pubmed:grant
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0013-7227
pubmed:author
pubmed:issnType
Print
pubmed:volume
147
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4036-43
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:16709608-Alkaline Phosphatase, pubmed-meshheading:16709608-Animals, pubmed-meshheading:16709608-Brain Chemistry, pubmed-meshheading:16709608-Cholesterol, pubmed-meshheading:16709608-Disease Models, Animal, pubmed-meshheading:16709608-Drug Resistance, pubmed-meshheading:16709608-Female, pubmed-meshheading:16709608-Humans, pubmed-meshheading:16709608-Hypothalamus, pubmed-meshheading:16709608-Kinetics, pubmed-meshheading:16709608-Liver, pubmed-meshheading:16709608-Male, pubmed-meshheading:16709608-Membrane Transport Proteins, pubmed-meshheading:16709608-Mice, pubmed-meshheading:16709608-Mice, Inbred C57BL, pubmed-meshheading:16709608-Mice, Knockout, pubmed-meshheading:16709608-Mutation, pubmed-meshheading:16709608-Phenotype, pubmed-meshheading:16709608-Thyroid Hormones, pubmed-meshheading:16709608-Thyrotropin, pubmed-meshheading:16709608-Thyroxine, pubmed-meshheading:16709608-Triiodothyronine
pubmed:year
2006
pubmed:articleTitle
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice.
pubmed:affiliation
Department of Medicine, University of Chicago, MC 3090, 5841 South Maryland Avenue, Chicago, Illinois 60637, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural