2017
DOI: 10.1182/blood-2017-05-783043
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Thyroid hormone regulates hematopoiesis via the TR-KLF9 axis

Abstract: Congenital hypothyroidism (CH) is one of the most prevalent endocrine diseases, for which the underlying mechanisms remain unknown; it is often accompanied by anemia and immunodeficiency in patients. Here, we created a severe CH model together with anemia and T lymphopenia to mimic the clinical features of hypothyroid patients by ethylnitrosourea (ENU) mutagenesis in Bama miniature pigs. A novel recessive c.1226A>G transition of the dual oxidase 2 () gene was identified as the causative mutation. This mutation… Show more

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Cited by 48 publications
(45 citation statements)
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“…Irrespective of AVP deficiency, patients with cDI generally have other factors influencing haematopoiesis, for example anterior pituitary deficiency with or without replacement therapy. Although there is evidence that thyroid hormones 18,19 and glucocorticosteroids 20‐22 have an impact on erythropoiesis, we did not find any association of hypothalamic‐pituitary‐thyroid hormone or HPA axis deficiency and altered haemoglobin levels in cDI patients. This is most likely explained by the euthyroid and euadrenal state of our patients under replacement therapy.…”
Section: Discussioncontrasting
confidence: 92%
“…Irrespective of AVP deficiency, patients with cDI generally have other factors influencing haematopoiesis, for example anterior pituitary deficiency with or without replacement therapy. Although there is evidence that thyroid hormones 18,19 and glucocorticosteroids 20‐22 have an impact on erythropoiesis, we did not find any association of hypothalamic‐pituitary‐thyroid hormone or HPA axis deficiency and altered haemoglobin levels in cDI patients. This is most likely explained by the euthyroid and euadrenal state of our patients under replacement therapy.…”
Section: Discussioncontrasting
confidence: 92%
“…Fatigue, one of the most common and debilitating symptoms in MPN patients, is reported in upwards of 93% of MPN patients, and is thought to be the largest contributor to reduced quality of life [2, 7]. Additionally, disease-related psychosocial sequelae, such as depression, are often refractory and undertreated [8, 9].…”
Section: Introductionmentioning
confidence: 99%
“…We have successfully established a systematic three-generation ENU mutagenesis porcine program and screened a large scale of mutants with a broad range of phenotypes that could be potentially developed into models for human diseases (Hai et al, 2017a, 2017b; Zhang et al, 2017). Forward genetic screening is an important method that can be used to establish human disease models and to facilitate studies of gene function (Hrabé de Angelis and Balling, 1998) due to the advantages like high throughput and identification of novel molecular signal pathways without prior hypothesis (de Bruijn et al, 2009).…”
Section: Discussionmentioning
confidence: 99%