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1.
Virchows Arch ; 479(1): 215-220, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-34028621

RESUMO

Multilocular thymic cyst (MTC) and germ cell tumors are common diseases that impact the mediastinum. Correctly diagnosing these diseases can be difficult because several other conditions can mimic them. We report a male patient with MTC associated with mediastinal seminoma. A needle biopsy of the mediastinal tumor revealed numerous epithelioid cell granulomas that mimicked sarcoidosis or mycobacterial infection. However, large atypical cells positive for Oct3/4 and KIT were noted between the granulomas; thus, we diagnosed the patient with mediastinal seminoma. The resected tumor, after chemotherapy, consisted of multiple cystic lesions, and a residual germ cell tumor was first considered. However, thymic medulla-specific elements, namely, POU2F3-positive thymic tuft cells and rhabdomyomatous myoid cells accompanying the epithelium, led to the correct diagnosis of MTC. Our case underscores the importance of recognizing the histological features associated with mediastinal seminoma and provides novel findings for MTC pathogenesis, namely, the presence of thymic tuft cells.


Assuntos
Biomarcadores Tumorais/análise , Proliferação de Células , Células Epitelioides , Cisto Mediastínico , Neoplasias do Mediastino , Fatores de Transcrição de Octâmero/análise , Seminoma , Biópsia por Agulha , Células Epitelioides/química , Células Epitelioides/patologia , Humanos , Masculino , Cisto Mediastínico/química , Cisto Mediastínico/patologia , Cisto Mediastínico/terapia , Neoplasias do Mediastino/química , Neoplasias do Mediastino/patologia , Neoplasias do Mediastino/terapia , Seminoma/química , Seminoma/patologia , Seminoma/terapia
2.
Methods ; 98: 158-165, 2016 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-26564236

RESUMO

A number of non-membranous cellular bodies have been identified in higher eukaryotes, and these bodies contain a specific set of proteins and RNAs that are used to fulfill their functions. The size of these RNA-containing cellular bodies is usually on a submicron scale, making it difficult to observe fine structures using optical microscopy due to the diffraction limitation of visible light. Recently, microscope companies have released super-resolution microscopes that were developed using different principles, enabling the observation of sub-micron structures not resolvable in conventional fluorescent microscopy. Here, we describe multi-color fluorescent in situ hybridization techniques optimized for the simultaneous detection of RNA and proteins using super-resolution microscopy, namely structured illumination microscopy (SIM).


Assuntos
Hibridização in Situ Fluorescente/métodos , Microscopia de Fluorescência/métodos , Sondas RNA/química , RNA Longo não Codificante/análise , Transcrição Gênica , Anticorpos/química , Biotina/química , Linhagem Celular , DNA Helicases/análise , DNA Helicases/genética , DNA Helicases/metabolismo , Proteínas de Ligação a DNA , Digitonina/química , Fluoresceína-5-Isotiocianato/química , Haptenos/química , Humanos , Imageamento Tridimensional , Proteínas Associadas à Matriz Nuclear/análise , Proteínas Associadas à Matriz Nuclear/genética , Proteínas Associadas à Matriz Nuclear/metabolismo , Proteínas Nucleares/análise , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Fatores de Transcrição de Octâmero/análise , Fatores de Transcrição de Octâmero/genética , Fatores de Transcrição de Octâmero/metabolismo , Fator de Processamento Associado a PTB/análise , Fator de Processamento Associado a PTB/genética , Fator de Processamento Associado a PTB/metabolismo , RNA Longo não Codificante/genética , RNA Longo não Codificante/metabolismo , Proteína FUS de Ligação a RNA/análise , Proteína FUS de Ligação a RNA/genética , Proteína FUS de Ligação a RNA/metabolismo , Proteínas de Ligação a RNA/análise , Proteínas de Ligação a RNA/genética , Proteínas de Ligação a RNA/metabolismo , Coloração e Rotulagem/métodos , Fatores de Transcrição/análise , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismo
3.
J Reprod Dev ; 57(3): 355-64, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21289464

RESUMO

The transition from male primitive germ cells (gonocytes) to type A spermatogonia in the neonatal testis is the initial process and a crucial process in spermatogenesis. However, in large domestic animals, the physiological and biochemical characteristics of germ cells during the developmental processes remain largely unknown. In this study, we characterized bovine germ cells in the developing testis from the neonatal stage to the adult stage. The binding of the lectin Dolichos biflorus agglutinin (DBA) and the expression of ubiquitin carboxyl-terminal hydrolase 1 (UCHL1) were restricted to gonocytes in the neonatal testis and spermatogonia in the adult testis. Gonocytes also expressed a germ cell marker (VASA) and stem cell markers (NANOG and OCT3/4), while the expressions of these markers in the adult testis were restricted to differentiated spermatic cells and were rarely expressed in spermatogonia. We subsequently utilized these markers to characterize gonocytes and spermatogonia after culture in vitro. Spermatogonia that were collected from the adult testis formed colonies in vitro only for one week. On the other hand, gonocytes from the neonatal testis could proliferate and form colonies after every passage for 1.5 months in culture. These colonies retained undifferentiated states of gonocytes as confirmed by the expression of both germ cell and stem cell markers. Moreover, a transplantation assay using immunodeficient mice testes showed that long-term cultured cells derived from gonocytes were able to colonize in the recipient testis. These results indicated that bovine gonocytes could maintain germ cell and stem cell potential in vitro.


Assuntos
Espermatogênese , Espermatogônias/crescimento & desenvolvimento , Testículo/crescimento & desenvolvimento , Animais , Biomarcadores/análise , Bovinos , Proliferação de Células , Células Cultivadas , Proteínas de Homeodomínio/análise , Masculino , Camundongos , Camundongos SCID , Fatores de Transcrição de Octâmero/análise , Espermatogônias/citologia , Células-Tronco/citologia , Células-Tronco/metabolismo , Testículo/citologia , Ubiquitina Tiolesterase/análise
4.
Protein J ; 28(3-4): 139-47, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19365714

RESUMO

Protein arginine methylation is found in many nucleic acid binding proteins affecting numerous cellular functions. In this study we identified methylarginine-containing proteins in HeLa cell extracts by two-dimensional electrophoresis and immunoblotting with a methylarginine-specific antibody. Protein spots with matched protein stain and blotting signals were analyzed by mass spectrometry. The identities of 12 protein spots as 11 different proteins were suggested. Known methylarginine-containing proteins such as hnRNP A2/B1, hnRNP A1, hnRNP G and FUS were identified, indicating the feasibility of our approach. However, four highly abundant metabolic enzymes that might co-electrophorese with methylarginine-containing proteins were also identified. Other nucleic acid binding proteins hnRNP M, hnRNP I and NonO protein were identified. Recombinant hnRNP M and a peptide with the RGG sequence in hnRNP M could be further methylated in vitro. The immunoblotting results of immunoprecipitated hnRNP I and NonO protein are consistent with arginine methylation in both proteins. In this study we identified methylarginine-containing proteins in HeLa cells through proteomic approaches and the method is fast and robust for further applications.


Assuntos
Arginina/análogos & derivados , Eletroforese em Gel Bidimensional/métodos , Immunoblotting/métodos , Sequência de Aminoácidos , Animais , Anticorpos/química , Especificidade de Anticorpos , Arginina/análise , Arginina/metabolismo , Proteínas de Ligação a DNA , Células HeLa , Ribonucleoproteína Nuclear Heterogênea A1 , Ribonucleoproteínas Nucleares Heterogêneas Grupo A-B/análise , Ribonucleoproteínas Nucleares Heterogêneas Grupo A-B/metabolismo , Ribonucleoproteínas Nucleares Heterogêneas Grupo M/análise , Ribonucleoproteínas Nucleares Heterogêneas Grupo M/metabolismo , Humanos , Metilação , Dados de Sequência Molecular , Proteínas Associadas à Matriz Nuclear/análise , Proteínas Associadas à Matriz Nuclear/metabolismo , Fatores de Transcrição de Octâmero/análise , Fatores de Transcrição de Octâmero/metabolismo , Mapeamento de Peptídeos , Processamento de Proteína Pós-Traducional , Proteína-Arginina N-Metiltransferases/metabolismo , Proteínas de Ligação a RNA/análise , Proteínas de Ligação a RNA/metabolismo , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz
5.
J Zoo Wildl Med ; 38(1): 150-3, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17469294

RESUMO

This report describes the gross, histologic, and immunohistochemical features of ovarian dysgerminomas in two adult female mountain chicken frogs (Leptodactylusfallax) from the same zoological institution. One frog was found dead, and the other frog had been ill for several days with a bloated abdomen and lethargy. On necropsy, large, pale multilobulated masses replaced the left ovary in both frogs, and one frog also had numerous smaller nodules scattered throughout the coelomic viscera. Histologically, these masses were composed of sheets and cords of polyhedral discrete germ cells consistent with the diagnosis of dysgerminoma. Neoplastic cells stained positive with immunohistochemistry for Oct4, which has been reported to detect stem cells including germ cells in a variety of species, including humans. Ovarian tumors are uncommonly encountered in both reptiles and amphibians, and this report is the first report of dysgerminoma in any amphibian species.


Assuntos
Anuros , Disgerminoma/veterinária , Neoplasias Ovarianas/veterinária , Animais , Animais de Zoológico , Biomarcadores Tumorais/análise , Disgerminoma/patologia , Evolução Fatal , Feminino , Metástase Neoplásica , Fatores de Transcrição de Octâmero/análise , Neoplasias Ovarianas/patologia
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