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2.
Surg Endosc ; 32(2): 617-626, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-28717870

RESUMO

BACKGROUND: Evidence on the value of laparoscopic liver resections (LLR) for hepatocellular carcinoma (HCC) and severe cirrhosis is still lacking. The aim of this study is to assess surgical and oncological outcomes of LLR in cirrhotic HCC patients. METHODS: The analysis included 403 LLR for HCC from seven European centres. 333 cirrhotic and 70 non-cirrhotic patients were compared. A matched comparison was performed between 100 Child-Pugh A and 25 Child-Pugh B patients. RESULTS: There was no difference in blood loss (250 vs. 250 mL, p 0.465) and morbidity (28.6 vs. 26.4%, p 0.473) between cirrhotics and non-cirrhotics, and liver-specific complications were similar (12.8 vs. 12%, p 0.924). The sub-analysis revealed similar perioperative outcomes in either Child-Pugh A or B patients. Noteworthy, ascitis (11 vs. 12%, p 0.562) and liver failure (3 vs. 4%, p 0.595) were not different. ASA score (OR 1.76, p 0.034) and conversion (OR 2.99, p 0.019) were risk factors for major morbidity. Despite lower recurrence-free survival in cirrhotics (43 vs. 55 months, p 0.034), overall survival was similar to non-cirrhotic patients (84 vs. 76.5, p 0.598). CONCLUSION: LLR for HCC appear equally safe in cirrhotic and non-cirrhotic patients, and the advantages can be witnessed in those with advanced cirrhosis. Severe comorbidities and conversion should be considered risk factors for complications-rather than the severity of cirrhosis and portal hypertension-when liver resection is performed laparoscopically. Such results may be of great interest to liver surgeons and hepatologists when deciding on the management of HCC within cirrhosis.


Assuntos
Carcinoma Hepatocelular/cirurgia , Hepatectomia , Hipertensão Portal/patologia , Laparoscopia , Cirrose Hepática/patologia , Neoplasias Hepáticas/cirurgia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Criança , Feminino , Hepatectomia/métodos , Humanos , Hipertensão Portal/cirurgia , Laparoscopia/métodos , Cirrose Hepática/cirurgia , Masculino , Pessoa de Meia-Idade , Adulto Jovem
3.
Dev Biol ; 366(2): 142-52, 2012 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-22537491

RESUMO

Regulated cell death, defined in morphological terms as apoptosis, is crucial for organ morphogenesis. While differentiation of the thyroid gland has been extensively studied, nothing is yet known about the survival mechanisms involved in the development of this endocrine gland. Using the zebrafish model system, we aim to understand whether genes belonging to the Bcl-2 family that control apoptosis are implicated in regulation of cell survival during thyroid development. Evidence of strong Bcl-2 gene expression in mouse thyroid precursors prompted us to investigate the functions played by its zebrafish homologs during thyroid development. We show that the bcl2-like (bcl2l) gene is expressed in the zebrafish thyroid primordium. Morpholino-mediated knockdown and mutant analyses revealed that bcl2l is crucial for thyroid cell survival and that this function is tightly modulated by the transcription factors pax2a, nk2.1a and hhex. Also, the bcl2l gene appears to control a caspase-3-dependent apoptotic mechanism during thyroid development. Thyroid precursor cells require an actively maintained survival mechanism to properly proceed through development. The bcl2l gene operates in the inhibition of cell death under direct regulation of a thyroid specific set of transcription factors. This is the first demonstration of an active mechanism to ensure survival of the thyroid primordium during morphogenesis.


Assuntos
Genes bcl-2 , Glândula Tireoide/embriologia , Proteínas de Peixe-Zebra/fisiologia , Peixe-Zebra/embriologia , Proteína bcl-X/fisiologia , Animais , Sobrevivência Celular , Morfogênese , Glândula Tireoide/fisiologia , Fatores de Transcrição/fisiologia
4.
Dev Biol ; 359(2): 163-75, 2011 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-21924257

RESUMO

The thyroid and lungs originate as neighboring bud shaped outgrowths from the midline of the embryonic foregut. When and how organ specific programs regulate development into structures of distinct shapes, positions and functions is incompletely understood. To characterize, at least in part, the genetic basis of these events, we have employed laser capture microdissection and microarray analysis to define gene expression in the mouse thyroid and lung primordia at E10.5. By comparing the transcriptome of each bud to that of the whole embryo as well as to each other, we broadly describe the genes that are preferentially expressed in each developing organ as well as those with an enriched expression common to both. The results thus obtained provide a valuable resource for further analysis of genes previously unrecognized to participate in thyroid and lung morphogenesis and to discover organ specific as well as common developmental mechanisms. As an initial step in this direction we describe a regulatory pathway involving the anti-apoptotic gene Bcl2 that controls cell survival in early thyroid development.


Assuntos
Embrião de Mamíferos/metabolismo , Pulmão/metabolismo , Glândula Tireoide/metabolismo , Transcriptoma , Animais , Padronização Corporal/genética , Sistema Digestório/embriologia , Sistema Digestório/metabolismo , Embrião de Mamíferos/embriologia , Feminino , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento , Hibridização In Situ , Microdissecção e Captura a Laser , Pulmão/embriologia , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Análise de Sequência com Séries de Oligonucleotídeos , Organogênese/genética , Glândula Tireoide/embriologia , Fatores de Tempo
5.
Nucleic Acids Res ; 38(10): 3172-85, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20123735

RESUMO

Activity of the sodium/iodide symporter (NIS) in lactating breast is essential for iodide (I(-)) accumulation in milk. Significant NIS upregulation was also reported in breast cancer, indicating a potential use of radioiodide treatment. All-trans-retinoic acid (tRA) is a potent ligand that enhances NIS expression in a subset of breast cancer cell lines and in experimental breast cancer models. Indirect tRA stimulation of NIS in breast cancer cells is very well documented; however, direct upregulation by tRA-activated nuclear receptors has not been identified yet. Aiming to uncover cis-acting elements directly regulating NIS expression, we screened evolutionary-conserved non-coding genomic sequences for responsiveness to tRA in MCF-7. Here, we report that a potent enhancer in the first intron of NIS mediates direct regulation by tRA-stimulated nuclear receptors. In vitro as well as in vivo DNA-protein interaction assays revealed direct association between retinoic acid receptor-alpha (RARalpha) and retinoid-X-receptor (RXR) with this enhancer. Moreover, using chromatin immunoprecipitation (ChIP) we uncovered early events of NIS transcription in response to tRA, which require the interaction of several novel intronic tRA responsive elements. These findings indicate a complex interplay between nuclear receptors, RNA Pol-II and multiple intronic RAREs in NIS gene, and they establish a novel mechanistic model for tRA-induced gene transcription.


Assuntos
Neoplasias da Mama/genética , Elementos Facilitadores Genéticos , Regulação Neoplásica da Expressão Gênica , Íntrons , Receptores do Ácido Retinoico/metabolismo , Simportadores/genética , Sequência de Bases , Neoplasias da Mama/metabolismo , Linhagem Celular Tumoral , Sequência Conservada , Feminino , Genômica , Humanos , RNA Polimerase II/metabolismo , Elementos de Resposta , Receptor alfa de Ácido Retinoico , Receptores X de Retinoides/metabolismo , Transcrição Gênica , Tretinoína/farmacologia
7.
BMC Dev Biol ; 11: 9, 2011 Feb 23.
Artigo em Inglês | MEDLINE | ID: mdl-21345181

RESUMO

BACKGROUND: The transcription factor Nkx2-1 (also known as TTF-1, Titf1 or T/EBP) contains two apparently redundant activation domains and is post-translationally modified by phosphorylation. We have generated mouse mutant strains to assess the roles of the two activation domains and of phosphorylation in mouse development and differentiation. RESULTS: Mouse strains expressing variants of the transcription factor Nkx2-1 deleted of either activation domain have been constructed. Phenotypic analysis shows for each mutant a distinct set of defects demonstrating that distinct portions of the protein endow diverse developmental functions of Nkx2-1. Furthermore, a mouse strain expressing a Nkx2-1 protein mutated in the phosphorylation sites shows a thyroid gland with deranged follicular organization and gene expression profile demonstrating the functional role of phosphorylation in Nkx2-1. CONCLUSIONS: The pleiotropic functions of Nkx2-1 are not all due to the protein as a whole since some of them can be assigned to separate domains of the protein or to specific post-translational modifications. These results have implication for the evolutionary role of mutations in transcription factors.


Assuntos
Proteínas Nucleares/metabolismo , Hipófise/embriologia , Processamento de Proteína Pós-Traducional , Glândula Tireoide/embriologia , Fatores de Transcrição/metabolismo , Animais , Diferenciação Celular , Imunofluorescência , Perfilação da Expressão Gênica , Técnicas de Introdução de Genes , Técnicas de Inativação de Genes , Genótipo , Hibridização In Situ , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Transgênicos , Mutação , Proteínas Nucleares/química , Proteínas Nucleares/genética , Análise de Sequência com Séries de Oligonucleotídeos , Fenótipo , Fosforilação , Estrutura Terciária de Proteína/genética , Deleção de Sequência , Relação Estrutura-Atividade , Glândula Tireoide/anormalidades , Fator Nuclear 1 de Tireoide , Fatores de Transcrição/química , Fatores de Transcrição/genética
8.
BMC Genomics ; 11: 306, 2010 May 14.
Artigo em Inglês | MEDLINE | ID: mdl-20470391

RESUMO

BACKGROUND: The molecular mechanisms leading to a fully differentiated thyrocite are still object of intense study even if it is well known that thyroglobulin, thyroperoxidase, NIS and TSHr are the marker genes of thyroid differentiation. It is also well known that Pax8, TTF-1, Foxe1 and Hhex are the thyroid-enriched transcription factors responsible for the expression of the above genes, thus are responsible for the differentiated thyroid phenotype. In particular, the role of Pax8 in the fully developed thyroid gland was studied in depth and it was established that it plays a key role in thyroid development and differentiation. However, to date the bases for the thyroid-enriched expression of this transcription factor have not been unraveled yet. Here, we report the identification and characterization of a functional thyroid-specific enhancer element located far upstream of the Pax8 gene. RESULTS: We hypothesized that regulatory cis-acting elements are conserved among mammalian genes. Comparison of a genomic region extending for about 100 kb at the 5'-flanking region of the mouse and human Pax8 gene revealed several conserved regions that were tested for enhancer activity in thyroid and non-thyroid cells. Using this approach we identified one putative thyroid-specific regulatory element located 84.6 kb upstream of the Pax8 transcription start site. The in silico data were verified by promoter-reporter assays in thyroid and non-thyroid cells. Interestingly, the identified far upstream element manifested a very high transcriptional activity in the thyroid cell line PC Cl3, but showed no activity in HeLa cells. In addition, the data here reported indicate that the thyroid-enriched transcription factor TTF-1 is able to bind in vitro and in vivo the Pax8 far upstream element, and is capable to activate transcription from it. CONCLUSIONS: Results of this study reveal the presence of a thyroid-specific regulatory element in the 5' upstream region of the Pax8 gene. The identification of this regulatory element represents the first step in the investigation of upstream regulatory mechanisms that control Pax8 transcription during thyroid differentiation and are relevant to further studies on Pax8 as a candidate gene for thyroid dysgenesis.


Assuntos
Elementos Facilitadores Genéticos/genética , Genômica , Fatores de Transcrição Box Pareados/genética , Glândula Tireoide/metabolismo , Região 5'-Flanqueadora/genética , Animais , Sequência Conservada , Proteínas de Ligação a DNA/metabolismo , Regulação da Expressão Gênica , Humanos , Camundongos , Especificidade de Órgãos , Fator de Transcrição PAX8 , Fatores de Transcrição Box Pareados/metabolismo , Filogenia , Alinhamento de Sequência , Homologia de Sequência do Ácido Nucleico , Glândula Tireoide/citologia , Fatores de Transcrição , Transcrição Gênica
9.
World J Gastrointest Endosc ; 11(4): 308-321, 2019 Apr 16.
Artigo em Inglês | MEDLINE | ID: mdl-31040892

RESUMO

BACKGROUND: Plasma-cell neoplasms rarely involve the gastrointestinal tract and manifest as gastrointestinal bleeding. Plasmablastic myeloma is an aggressive plasma cell neoplasm associated with poor outcomes. A small number of cases with gastrointestinal involvement is reported in the literature and therefore high index of suspicion is essential for avoiding delays in diagnosis and treatment. CASE SUMMARY: Our aim is to present our experience of a 70-year-old patient with a secondary presentation of plasmablastic myeloma manifesting as unstable upper gastrointestinal bleeding and to review the literature with the view to consolidate and discuss information about diagnosis and management of this rare entity. In addition to our case, a literature search (PubMed database) of case reports of extramedullary plasma cell neoplasms manifesting as upper gastrointestinal bleeding was performed. Twenty-seven cases of extramedullary plasmacytoma (EMP) involving the stomach and small bowel presenting with upper gastrointestinal bleeding were retrieved. The majority of patients were males (67%). The average age on diagnosis was 62.7 years. The most common site of presentation was the stomach (41%), followed by the duodenum (15%). The most common presenting complaint was melena (44%). In the majority of cases, the EMPs were a secondary manifestation (63%) at the background of multiple myeloma (26%), plasmablastic myeloma (7%) or high-grade plasma cell myeloma (4%). Oesophagogastroscopy was the main diagnostic modality and chemotherapy the preferred treatment option for secondary EMPs. CONCLUSION: Despite their rare presentation, upper gastrointestinal EMPs should be considered in the differential diagnosis of patients with gastrointestinal bleeding especially in the presence of systemic haematological malignancy.

10.
Arq. bras. neurocir ; 43(3): 200-203, 2024.
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1571423

RESUMO

Introduction Optimal surgical treatment for chronic subdural hematoma (CSDH) in the elderly has been controversial. Whenever possible, a less invasive technique should be used to avoid complications. Case Report The patient was 82-years-old, with JPS; with diagnosis of liver cirrhosis due to alcohol abuse and history of recent myocardial infarction. He was admitted to the emergency room with temporal-spatial disorientation. The Glasgow coma scale (GCS) value on admission was 9. Left hemiparesis and osteotendinous hyperreflexia in the left side of the body. Noncontrast-enhanced cranial computed tomography (CT) showed right frontoparietal hypodense lesion with mass effect. Due to the clinical conditions of the patient, drainage of the hematoma was indicated through local anesthesia and sedation with midazolam. He was discharged after 8 days with improvement in his mental and neurological condition. Conclusion Drainage of CSDH using local anesthesia in an elderly person with severe comorbidity can reach excellent results.


Introdução O tratamento cirúrgico ideal para hematoma subdural crônico (HSDC) em idosos tem sido controverso. Sempre que possível uma técnica menos invasiva deve ser utilizada para evitar complicações. Relato do Caso Paciente de 82 anos portadora de JPS; com diagnóstico de cirrose hepática por abuso de álcool e história de infarto do miocárdio recente. Foi admitido no pronto-socorro com desorientação espaço-temporal. O valor da escala de coma de Glasgow (ECG) na admissão era 9. Hemiparesia esquerda e hiperreflexia osteotendinosa no lado esquerdo do corpo. A tomografia computadorizada (TC) de crânio sem contraste mostrou lesão frontoparietal hipodensa direita com efeito de massa. Devido às condições clínicas do paciente foi indicada drenagem do hematoma através de anestesia local e sedação com midazolam. Teve alta após 8 dias com melhora do quadro mental e neurológico. Conclusão A drenagem do HDC com anestesia local em idoso com comorbidade grave pode alcançar excelentes resultados.

11.
Endocr Rev ; 25(5): 722-46, 2004 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15466939

RESUMO

Thyroid gland organogenesis results in an organ the shape, size, and position of which are largely conserved among adult individuals of the same species, thus suggesting that genetic factors must be involved in controlling these parameters. In humans, the organogenesis of the thyroid gland is often disturbed, leading to a variety of conditions, such as agenesis, ectopy, and hypoplasia, which are collectively called thyroid dysgenesis (TD). The molecular mechanisms leading to TD are largely unknown. Studies in murine models and in a few patients with dysgenesis revealed that mutations in regulatory genes expressed in the developing thyroid are responsible for this condition, thus showing that TD can be a genetic and inheritable disease. These studies open the way to a novel working hypothesis on the molecular and genetic basis of this frequent human condition and render the thyroid an important model in the understanding of molecular mechanisms regulating the size, shape, and position of organs.


Assuntos
Doenças da Glândula Tireoide/genética , Glândula Tireoide/anormalidades , Glândula Tireoide/embriologia , Animais , Diferenciação Celular , Coristoma , Humanos , Mutação , Proteínas Nucleares/genética , Proteínas Nucleares/fisiologia , Organogênese/genética , Glândula Tireoide/crescimento & desenvolvimento , Hormônios Tireóideos/biossíntese , Fator Nuclear 1 de Tireoide , Fatores de Transcrição/genética , Fatores de Transcrição/fisiologia
12.
Mol Cell Biol ; 25(22): 10171-82, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16260629

RESUMO

Thyroid transcription factor gene 1 (TTF-1) is a homeobox-containing gene involved in thyroid organogenesis. During early thyroid development, the homeobox gene Nkx-2.5 is expressed in thyroid precursor cells coincident with the appearance of TTF-1. The aim of this study was to investigate the molecular mechanisms underlying thyroid-specific gene expression. We show that the Nkx-2.5 C terminus interacts with the TTF-1 homeodomain and, moreover, that the expression of a dominant-negative Nkx-2.5 isoform (N188K) in thyroid cells reduces TTF-1-driven transcription by titrating TTF-1 away from its target DNA. This process reduced the expression of several thyroid-specific genes, including pendrin and thyroglobulin. Similarly, down-regulation of TTF-1 by RNA interference reduced the expression of both genes, whose promoters are sensitive to and directly associate with TTF-1 in the chromatin context. In conclusion, we demonstrate that pendrin and thyroglobulin are downstream targets in vivo of TTF-1, whose action is a prime factor in controlling thyroid differentiation in vivo.


Assuntos
Antiportadores de Cloreto-Bicarbonato/fisiologia , Regulação da Expressão Gênica , Proteínas de Membrana Transportadoras/fisiologia , Proteínas Nucleares/fisiologia , Neoplasias da Glândula Tireoide/metabolismo , Fatores de Transcrição/fisiologia , Animais , Sequência de Bases , Sítios de Ligação , Northern Blotting , Western Blotting , Diferenciação Celular , Antiportadores de Cloreto-Bicarbonato/metabolismo , Cromatina , Imunoprecipitação da Cromatina , DNA/química , Regulação para Baixo , Genes Dominantes , Células HeLa , Humanos , Imunoprecipitação , Íntrons , Íons , Proteínas de Membrana Transportadoras/metabolismo , Dados de Sequência Molecular , Proteínas Nucleares/química , Oligonucleotídeos/química , Plasmídeos/metabolismo , Ligação Proteica , Isoformas de Proteínas , Estrutura Terciária de Proteína , Interferência de RNA , RNA Mensageiro/metabolismo , Ratos , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Transportadores de Sulfato , Glândula Tireoide/metabolismo , Fator Nuclear 1 de Tireoide , Fatores de Transcrição/química , Transfecção
13.
Endocrinology ; 148(6): 2737-46, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17347311

RESUMO

We have conditionally inactivated the E-cadherin gene in the thyroid follicular cells of mouse embryo to unravel its role in thyroid development. We used the Cre-loxP system in which the Cre-recombinase was expressed under the control of the tissue-specific thyroglobulin promoter that becomes active at embryonic d 15. At postnatal d 7, thyroid follicle lumens in the knockout mice were about 30% smaller with respect to control mice and had an irregular shape. E-cadherin was almost completely absent in thyrocytes, beta-catenin was significantly reduced, whereas no change in gamma-catenin was detected. alpha-Catenin was also reduced on the cell plasma membrane. Despite the dramatic loss of E-cadherin and beta-catenin, cell-cell junctions were not affected, the distribution of tight junction proteins was unaltered, and no increase of thyroglobulin circulating in the blood was observed. In addition, we found that other members of the cadherin family, the R-cadherin and the Ksp-cadherin, were expressed in thyrocytes and that their membrane distribution was not altered in the E-cadherin conditional knockout mouse. Our results indicate that E-cadherin has a role in the development of the thyroid gland and in the expression of beta-catenin, but it is not essential for the maintenance of follicular cell adhesion.


Assuntos
Caderinas/genética , Caderinas/fisiologia , Glândula Tireoide/embriologia , Glândula Tireoide/metabolismo , Junções Íntimas/metabolismo , Animais , Caderinas/metabolismo , Adesão Celular/genética , Claudina-1 , Feminino , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento , Masculino , Proteínas de Membrana/metabolismo , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Ocludina , Fosfoproteínas/metabolismo , Gravidez , Glândula Tireoide/anatomia & histologia , Junções Íntimas/genética , Proteína da Zônula de Oclusão-1 , beta Catenina/genética , beta Catenina/metabolismo
14.
J Endocrinol ; 192(3): 615-26, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17332529

RESUMO

In the thyroid, H(2)O(2) is produced at the apical pole of thyrocytes by one or two NADPH oxidases (NOX), Duox1/2 proteins. The onset of Duox expression was analysed by immunohistochemistry in the developing mouse thyroid in parallel with thyroglobulin (Tg) iodination and the expression of other thyroid differentiation markers. Duox proteins were found at embryonic day (E) 15.5 and were mainly localised at the apical pole of thyrocytes. Tg was detected 1 day before (E14.5) and Tg iodination was concomitant with the expression of both Duox and Na(+)/I(-) symporter (NIS; E15.5). The role of TSH in regulating Duox expression and H(2)O(2) accumulation was evaluated in thyroids of adult mice with reduced (Tshr(hyt/hyt) or mice treated with thyroxine) or increased (methimazole or perchlorate treatment) TSH/Tshr activity. In mice with suppressed TSH/Tshr activity, Duox expression was only partially decreased when compared with wild-type, as observed by western blot. In Tshr(hyt/hyt) strain, Duox was still expressed at the apical pole and H(2)O(2) measurements were normal. On the other hand, chronic TSH stimulation of the gland led to a decrease of H(2)O(2) measurements without affecting Duox expression. The onset of Duox protein expression is compatible with their proposed function in thyroid hormone synthesis and it can be considered as a functional marker of the developing thyroid. However, Duox expression in adult is much less regulated by TSH than NIS and thyroperoxidase. It is not always correlated with the overall thyroid H(2)O(2) accumulation, highlighting the importance of additional regulatory mechanisms which control either the production or H(2)O(2) degradation.


Assuntos
Flavoproteínas/análise , Regulação da Expressão Gênica no Desenvolvimento , Peróxido de Hidrogênio/análise , NADPH Oxidases/análise , Glândula Tireoide/embriologia , Animais , Western Blotting/métodos , Hipotireoidismo Congênito/embriologia , Hipotireoidismo Congênito/metabolismo , Oxidases Duais , Feminino , Imuno-Histoquímica , Iodeto Peroxidase/metabolismo , Camundongos , Camundongos Endogâmicos , Camundongos Mutantes , Modelos Animais , Gravidez , Receptores da Tireotropina/metabolismo , Tireoglobulina/metabolismo , Glândula Tireoide/química , Glândula Tireoide/metabolismo , Tireotropina/sangue , Tireotropina/farmacologia
15.
Mol Cell Biol ; 24(13): 5788-96, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15199135

RESUMO

The development and the function of central nervous system depend on thyroid hormones. In humans, the lack of thyroid hormones causes cretinism, a syndrome of severe mental deficiency. It is assumed that thyroid hormones affect the normal development and function of the brain by activating or suppressing target gene expression because several genes expressed in the brain have been shown to be under thyroid hormone control. Among these, the Rhes gene, encoding a small GTP-binding protein, is predominantly expressed in the striatal region of the brain. To clarify the role of Rhes in vivo, we disrupted the Rhes gene by homologous recombination in embryonic stem cells and generated mice homozygous for the Rhes null mutation (Rhes(-/-)). Rhes(-/-) mice were viable but weighed less than wild-type mice. Furthermore, they showed behavioral abnormalities, displaying a gender-dependent increase in anxiety levels and a clear motor coordination deficit but no learning or memory impairment. These results suggest that Rhes disruption affects selected behavioral competencies.


Assuntos
Corpo Estriado/fisiologia , Proteínas de Ligação ao GTP/fisiologia , Fatores Etários , Animais , Ansiedade , Peso Corporal , Química Encefálica/fisiologia , Corpo Estriado/química , Corpo Estriado/crescimento & desenvolvimento , Embrião de Mamíferos , Feminino , Proteínas de Ligação ao GTP/análise , Proteínas de Ligação ao GTP/genética , Regulação da Expressão Gênica no Desenvolvimento , Masculino , Camundongos , Camundongos Knockout , Transtornos das Habilidades Motoras , RNA Mensageiro/análise , Fatores Sexuais
16.
Endocr Dev ; 10: 1-14, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17684386

RESUMO

Gene targeting technology has allowed the generation of mouse mutants which lack specific genes. These mice represent a valuable tool for identifying the in vivo functions of proteins and for dissecting the pathways that control the development and differentiation of the numerous structures of the body. What we know about thyroid morphogenesis is largely due to studies on murine models generated in gene-targeting experiments. Although several points remain to be elucidated, a number of genes involved in thyroid organogenesis have been identified in recent years. In addition, this information has greatly improved our knowledge of the pathogenetic mechanisms of thyroid dysgenesis in humans. This review summarizes the complex processes leading to thyroid development mostly by describing the phenotype of currently available knockout animals.


Assuntos
Camundongos , Modelos Animais , Glândula Tireoide/embriologia , Animais , Desenvolvimento Embrionário/genética , Humanos , Mutação , Disgenesia da Tireoide/genética
17.
Mol Endocrinol ; 20(8): 1810-24, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16613988

RESUMO

Among the approaches used to provide a functional inactivation of a target protein, we have chosen the recently described oligomerization chain reaction (OCR) strategy to functionally inactivate the transcription factor Pax8, a member of the Pax gene family expressed in thyroid cells. The OCR strategy is based on the fusion of the self-associating coiled-coil (CC) domain of the nuclear factor promyelocytic leukemia (PML) to target proteins that are able to self-associate naturally or that form heterocomplexes. In the thyroid tissue, the transcription factor Pax8 is involved in the morphogenesis of the gland and in the transcriptional regulation of thyroid-expressed genes. We have recently demonstrated that in thyroid cells Pax8 interacts biochemically and functionally with the transcription factor TTF-1 (thyroid transcription factor 1), and that such interaction leads to the synergistic activation of thyroglobulin (Tg) gene expression. Fusion of the CC domain to Pax8 leads to the formation of aberrant, nonfunctional high-molecular mass complexes to which TTF-1 is also recruited. The CC-Pax8 chimera inhibits the transcriptional activity of Pax8 and of TTF-1 on both synthetic and physiological promoters and prevents the synergistic activation of the Tg promoter mediated by these two transcription factors. Furthermore, the expression of the CC-Pax8 chimera in differentiated thyroid cells leads to the down-regulation of the endogenous expression of several differentiation markers such as Tg, sodium/iodide symporter, Foxe1, TTF-1, and thyroid oxidase 2. These results demonstrate that the OCR is a useful tool to functionally inactivate a transcription factor. Moreover, by this approach, we identified Foxe1, TTF-1, and thyroid oxidase 2 as new direct targets of Pax8 or TTF-1.


Assuntos
Inativação Gênica , Fatores de Transcrição Box Pareados/fisiologia , Polímeros/metabolismo , Fatores de Transcrição/fisiologia , Biomarcadores , Diferenciação Celular , Células Cultivadas , Proteínas de Ligação a DNA/metabolismo , Oxidases Duais , Flavoproteínas/genética , Flavoproteínas/metabolismo , Fatores de Transcrição Forkhead/genética , Fatores de Transcrição Forkhead/metabolismo , Expressão Gênica , Células HeLa , Humanos , NADPH Oxidases/genética , NADPH Oxidases/metabolismo , Especificidade de Órgãos , Fator de Transcrição PAX8 , Fatores de Transcrição Box Pareados/metabolismo , Estrutura Terciária de Proteína , Proteínas Recombinantes de Fusão/metabolismo , Glândula Tireoide/citologia , Distribuição Tecidual , Fatores de Transcrição/metabolismo , Transfecção
18.
J Clin Endocrinol Metab ; 91(4): 1428-33, 2006 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16418214

RESUMO

CONTEXT: Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000-4000 at birth. In 80-85% of cases, CH is caused by defects in thyroid organogenesis, resulting in absent, ectopically located, and/or severely reduced gland [thyroid dysgenesis (TD)]. Mutations in genes controlling thyroid development have demonstrated that in a few cases, TD is a Mendelian trait. However, accumulating evidence supports the view that the genetics of TD are complex, possibly with a polygenic/multifactorial basis. A higher prevalence of congenital heart disease has been documented in children with CH than in the general population. Such an association suggests a possible pathogenic role of genes involved in both heart and thyroid development. NKX2-5 encodes a homeodomain-containing transcription factor with a major role in heart development, and mutations affecting this gene have been reported in individuals with congenital heart disease. OBJECTIVE: In the present work we investigated the possible involvement of NKX2-5 mutations in TD. RESULTS: Our results indicate that Nkx2-5(-/-) embryos exhibit thyroid bud hypoplasia, providing evidence that NKX2-5 plays a role in thyroid organogenesis and that NKX2-5 mutations contribute to TD. NKX2-5 mutational screening in 241 patients with TD allowed the identification of three heterozygous missense changes (R25C, A119S, and R161P) in four patients with TD. Functional characterization of the three mutations demonstrated reduced DNA binding and/or transactivation properties, with a dominant-negative effect on wild-type NKX2-5. CONCLUSION: Our results suggest a previously unknown role of NKX2-5 in the pathogenesis of TD.


Assuntos
Hipotireoidismo Congênito/genética , Proteínas de Homeodomínio/genética , Mutação de Sentido Incorreto/fisiologia , Fatores de Transcrição/genética , DNA/biossíntese , DNA/genética , Proteína Homeobox Nkx-2.5 , Humanos , Imuno-Histoquímica , Hibridização In Situ , Iodeto Peroxidase/metabolismo , Fenótipo , RNA Mensageiro/biossíntese , RNA Mensageiro/genética , Tireoglobulina/metabolismo , Glândula Tireoide/fisiologia
19.
Gene ; 374: 50-7, 2006 Jun 07.
Artigo em Inglês | MEDLINE | ID: mdl-16516413

RESUMO

Free D-aspartic acid and NMDA are present in the mammalian central nervous system and endocrine glands at significant concentrations, but their physiological role is still matter of debate. The only enzyme known to metabolize in vitro selectively these D-amino acids is D-aspartate oxidase (DDO). To clarify the role in vivo of the enzyme, we generated mice with targeted deletion of Ddo gene by homologous recombination. Mutated animals showed increased amounts of both D-aspartic acid and NMDA in all tissues examined demonstrating a physiological role of DDO in the regulation of their endogenous levels.


Assuntos
D-Aspartato Oxidase/deficiência , Ácido D-Aspártico/fisiologia , Regulação Enzimológica da Expressão Gênica , N-Metilaspartato/fisiologia , Animais , D-Aspartato Oxidase/genética , Ácido D-Aspártico/metabolismo , Ácido D-Aspártico/farmacologia , DNA Complementar , Perfilação da Expressão Gênica , Biblioteca Gênica , Marcação de Genes , Homozigoto , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , N-Metilaspartato/metabolismo , N-Metilaspartato/farmacologia , Distribuição Tecidual
20.
Oncol Rep ; 16(5): 1015-20, 2006 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17016586

RESUMO

PAX8 is a transcription factor with a role in ontogenesis of the urinary tract. The aim of the present investigation was to investigate PAX8 expression in normal bladder and in non-invasive urothelial tumours. Nine cases of normal urothelial mucosa, 2 cases of papillary urothelial neoplasia of low malignant potential, 12 cases of low grade non-invasive papillary urothelial carcinoma and 16 cases of high grade non-invasive papillary urothelial carcinoma were investigated by immunohistochemistry. PAX8 mRNA expression was evaluated by RT-PCR in a different set of normal bladder mucosas and tumours. In addition, PAX8 expression was evaluated by RT-PCR in bladder from 2 human embryos and in several continuous cell lines derived from bladder tumours (5637, RT-112, TCC-SUP, HT 1376). In immunohistochemical studies, PAX8 was expressed in 28 out of 30 non-invasive urothelial tumours, but not in the normal adult bladders. In RT-PCR studies, PAX8 was expressed in 13 out of 13 bladder tumours but not in the 6 normal bladder mucosa. Contrary to that in adults, PAX8 was expressed in 2 cases of bladder mucosa from 16-week-old embryos. PAX8 was expressed in all the cell lines from bladder tumours. Both in the bladder tumours and cell lines PAX8 expression was highly heterogeneous in terms of the splicing isoforms. Treatment of cell lines with sodium butyrate (NaB) induced several changes of the splicing isoforms. Therefore, only subsets of molecular events that determine the PAX8 mRNA splicing heterogeneity in bladder tumours are sensitive to NaB treatment.


Assuntos
Fatores de Transcrição Box Pareados/biossíntese , Neoplasias da Bexiga Urinária/metabolismo , Processamento Alternativo , Linhagem Celular Tumoral , Sistema Enzimático do Citocromo P-450 , Humanos , Imuno-Histoquímica , Oxigenases de Função Mista , Fator de Transcrição PAX8 , Fatores de Transcrição Box Pareados/genética , RNA Mensageiro/biossíntese , RNA Mensageiro/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa/métodos , Bexiga Urinária/metabolismo , Neoplasias da Bexiga Urinária/genética , Neoplasias da Bexiga Urinária/patologia
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