Searchable abstracts of presentations at key conferences in endocrinology

ea0063oc9.2 | Thyroid 2 | ECE2019

Direct evidence for disulfides in the mechanism of deiodinase 1

Rodriguez Alfonso Ruben Ruiz , Braun Doreen , Schweizer Ulrich

The main product of the thyroid gland, T4, is a prohormone. 5’-deiodination is needed to convert T4 into the active, nuclear receptor-binding hormone, T3. Pharmacological modulation of activating 5’-and inactivating 5-deiodination of iodothyronines would be desirable in a number of medical conditions, including hypothyroidism, hyperthyroidism and various cancers. A structural and mechanistic understanding of deiodinase (DIO) catalysis...

ea0014s14.3 | Trojan horses for steroids | ECE2007

Hepatic deiodinase activity is dispensable for the maintenance of normal thyroid hormone levels in mice

Schweizer Ulrich

The main product of the thyroid is thyroxine (T4). However, the physiological ligand of nuclear thyroid hormone receptors is triiodothyronine, T3. Deiodination of T4 to yield T3 is achieved by 5′-deiodinase activity. Type I-deiodinase (Dio1) was the first deiodinase cloned and its strong expression in liver and kidny, together with the size of these organs, suggested a role for Dio1 in peripheral conversion of T4 to T3. Later, Dio2 and Dio3 were cloned, enzymes with a mo...

ea0041gp191 | Thyroid - Basic | ECE2016

Chemical chaperones rescue pathogenic MCT8 mutations

Braun Doreen , Schweizer Ulrich

Introduction: Monocarboxylate transporter 8 (MCT8) is a thyroid hormone-specific transmembrane transport protein. Inactivating mutations in MCT8 lead to severe mental retardation, the Allan-Herndon-Dudley syndrome. The severity of the Allan-Herndon-Dudley syndrome differs among MCT8 patients. Partial activity of MCT8 can be caused either by mutations affecting the transport mechanism (e.g. substrate interaction, conformational change) or by inefficient protein expression, memb...

ea0035oc7.4 | IGF-1 and Thyroid Basic | ECE2014

Training MCT10 to transport thyroxine: Structure based targeted mutations in MCT10

Schweizer Ulrich , Braun Doreen , Johannes Jorg

With the identification of mutations in the monocarboxylate transporter 8 (MCT8) gene in patients afflicted with the Allan–Herndon–Dudley syndrome (AHDS), the concept of transporter-mediated transmembrane transport of thyroid hormones was finally accepted. Impaired thyroid hormone transport into neurons and pituitary cells is believed to cause severe psychomotor retardation and altered thyroid hormone function tests. MCT8 is a specific thyroid hormone transporter abl...

ea0016p737 | Thyroid | ECE2008

Role of deiodinases in the thyroid for the maintenance of circulating T3 levels

Chiu Jazmin , Wirth Eva , Schweizer Ulrich

Deiodinases (Dio1-3) are selenium-dependent enzymes that catalyze the reductive removal of iodine from iodothyronines. Depending on the substrate and the position of the iodine removed, deiodination can generate T3 from T4 or inactivate T3 and T4. Local expression of Dio can help to adjust the intracellular levels of T3 to the physiological needs of the organ without changing circulating T3 concentrations. It has been suggested that hepatic Dio1 generates circulating T3. Howev...

ea0020oc5.1 | Thyroid: Basic and Clinical | ECE2009

Neurological and behavioral phenotypes in mice lacking Mct8-mediated neuronal T3 uptake

Schweizer Ulrich , Wirth Eva , Roth Stephan , Kohrle Josef , Gruters Annette

Thyroid hormone transport into cells critically depends on plasma membrane transport proteins. One of these, monocarboxylate transporter 8 (MCT8), is mutated in patients suffering from a form of X-linked mental retardation, the Allan-Herndon-Dudley syndrome. These patients are characterized by abnormal thyroid hormone and TSH plasma levels indicating a role for MCT8 in the regulation of the thyroid hormone axis. Mice lacking the Mct8 gene replicate the thyroid hormone a...

ea0020p573 | Neuroendocrinology, Pituitary and Behaviour | ECE2009

Transport activities and plasma membrane localization of MCT8 mutant proteins identified in patients with severe psychomotor retardation depend on cell type. Implications for the interpretation of clinical phenotypes

Kinne Anita , Roth Stephan , Schweizer Ulrich , Kohrle Joseph

Objective: Mutations in the gene encoding the thyroid hormone transport protein, monocarboxylate transporter 8 (MCT8), underlie severe mental retardation. In vitro expression of mutant transporters was performed to understand phenotypical differences.Methods: We established cell lines stably expressing 16 MCT8 variants in JEG1 and MDCK cells. Several of these mutants have never been analysed before. The cell lines were characterized according to M...

ea0011oc63 | ThyroidOC57 British Thyroid Association Award | ECE2006

Gender-specific differences in the expression of deiodinase I (Dio1) in mammals

Riese C , Schweizer U , Köhrle J , Schomburg L

Selenium (Se) represents an essential trace element and acts as catalytic entity in thyroid hormone deiodinases (Dio), glutathione peroxidases or thioredoxin reductases. Se-deficiencies worsen a variety of conditions of which some display a sex-bias, including certain forms of cancer, autoimmune- and infectious diseases. Using C57BI/6 mice as model organism, we determined enzymatic activities and transcript levels of certain selenoproteins in various tissues. mRNA levels of th...

ea0081ep692 | Pituitary and Neuroendocrinology | ECE2022

Soluble alpha klotho in blood is a new and highly stable biomarker

Ribeiro de Oliveira Longo Schweizer Junia , Haenelt Michael , Schilbach Katharina , Stormann Sylvere , Schopohl Jochen , Bidlingmaier Martin

Background: Soluble alpha klotho (sαKL) is a circulating protein that has been linked to the growth hormone (GH) axis. We previously showed its association to disease activity in patients with acromegaly, with considerable robustness towards biological confounders. However, there is scarce data in literature regarding the analytical performance of the assay, and pre-analytical stability of sαKL in blood samples. Objective: We aimed to evaluate ...

ea0090ep761 | Pituitary and Neuroendocrinology | ECE2023

Delayed onset of pasireotide-induced hyperglycemia: Report of two cases

Stormann Sylvere , Schilbach Katharina , Amereller Felix , Schweizer Junia Ribeiro de Oliveira Longo , Schopohl Jochen

Introduction: Pasireotide is a potent somatostatin analogue (SSA) and used in therapy-refractory acromegaly, commonly after failure of treatment with first-generation SSA. However, it may induce severe hyperglycemia, which usually occurs rapidly after initiation of therapy and in general gradually improves over time. We here present two cases of young male patients who developed severe pasireotide-induced hyperglycemia after several years of treatment.Ca...