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1.
Int. j. morphol ; 37(4): 1203-1209, Dec. 2019. graf
Article in English | LILACS | ID: biblio-1040112

ABSTRACT

In vitro modeling of neurodegenerative diseases is now possible by using patient-derived induced pluripotent stem cells (iPS). Through them, it is nowadays conceivable to obtain human neurons and glia, and study diseases cellular and molecular mechanisms, an attribute that was previously unavailable to any human condition. Amyotrophic lateral sclerosis (ALS) is one of the diseases that has gained a rapid advance with iPS technology. By differentiating motor neurons from iPS cells of ALS- patients, we are studying the mechanisms underlying ALS- disease onset and progression. Here, we introduce a cellular platform to help maintain longevity of ALS iPS-motor neurons, a cellular feature relevant for most late-onset human diseases. Long term cultures of patient-derived iPS cells might prove to be critical for the development of personalized-drugs.


Actualmente es posible modelar in vitro enfermedades neurodegenerativas humanas mediante el uso de células madre pluripotentes inducidas (iPS) derivadas del paciente. A través de ellas, es hoy concebible obtener neuronas y glía humanas, y estudiar mecanismos celulares y moleculares de enfermedades, un atributo que anteriormente no era posible para ninguna condición humana. La esclerosis lateral amiotrófica (ELA) es una de las enfermedades que se ha beneficiado con la tecnología de iPS. Al diferenciar neuronas motoras de células iPS obtenidas de pacientes con ELA, hemos iniciado estudios sobre los mecanismos que subyacen a la aparición y progresión de la enfermedad. Aquí, presentamos el desarrollo de una plataforma celular que permite extender la longevidad de las neuronas motoras derivadas de iPS, una característica relevante para la mayoría de las enfermedades humanas de inicio tardío. Los cultivos a largo plazo de células iPS provenientes de pacientes pueden ser determinantes en el desarrollo de terapias asociadas a la medicina de precisión.


Subject(s)
Humans , Animals , Mice , Induced Pluripotent Stem Cells/cytology , Amyotrophic Lateral Sclerosis/metabolism , Immunohistochemistry , Cell Line , Coculture Techniques , Amyotrophic Lateral Sclerosis/pathology , Amyotrophic Lateral Sclerosis/therapy
2.
Braz. j. med. biol. res ; 33(8): 897-903, Aug. 2000. ilus, tab
Article in English | LILACS | ID: lil-265846

ABSTRACT

We describe here the isolation and characterization of a major albumin from the seeds of Cereus jamacaru (Cactaceae), to which we gave the trivial name of cactin. This protein has a molecular mass of 11.3 kDa and is formed by a light chain (3.67 kDa) and a heavy chain (7.63 kDa). This protein was isolated using a combination of gel filtration chromatography and reverse-phase HPLC. The amino acid composition of cactin was determined and found to resemble that of the 2S seed reserve protein from the Brazil nut, a protein remarkable for its high methionine content. The usefulness of cactin as a molecular marker in the taxonomy of the Cactaceae is discussed


Subject(s)
Albumins/analysis , Methionine/analysis , Plant Proteins/analysis , Seeds/chemistry , Chromatography, High Pressure Liquid , Electrophoresis, Polyacrylamide Gel , Methionine/chemistry , Plant Proteins/chemistry
3.
Braz. j. med. biol. res ; 31(6): 757-61, jun. 1998. ilus, tab, graf
Article in English | LILACS | ID: lil-210962

ABSTRACT

We describe here the isolation and characterization of a major albumin from the seeds of Opuntia ficus-indica (Cactaceae). This protein has a molecular mass of 6.5 kDa and was isolated by a combination of gel filtration chromatography and reverse-phase HPLC. The amino acid composition of this protein was determined and it was shown to have similarities with the amino acid composition of several proteins from the 2S albumin storage protein family. The N-terminal amino acid sequence of this protein is Asp-Pro-Tyr-Trp-Glu-Gln-Arg


Subject(s)
Proteins/chemistry , Proteins/isolation & purification , Seeds/chemistry , Albumins/chemistry , Albumins/isolation & purification , Amino Acids/analysis , Amino Acids/chemistry , Chromatography, Gel , Chromatography, High Pressure Liquid
5.
J. pediatr. (Rio J.) ; 51(5/6): 325-7, 1981.
Article in Portuguese | LILACS | ID: lil-6276

ABSTRACT

Relatam-se cinco casos de meninos, com idades entre sete meses e sete anos que apresentavam sangramento retal. Apos investigacao de rotina o enema opaco pela tecnica do duplo contraste revelou hiperplasia linfoide benigna do colon. O sangramento retal desapareceu sem tratamento, confirmando a evolucao usualmente benigna desta entidade


Subject(s)
Colonic Diseases , Lymphatic Diseases , Hyperplasia
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