Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros










Intervalo de ano de publicação
1.
Stem Cell Rev Rep ; 10(3): 429-46, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24619862

RESUMO

Cryopreservation is the only method for long-term storage of viable cells and tissues used for cellular therapy, stem cell transplantation and/or tissue engineering. However, the freeze-thaw process strongly contributes to cell and tissue damage through several mechanisms, including oxidative stress, cell injury from intracellular ice formation and altered physical cellular properties. Our previous proteomics investigation was carried out on Wharton's Jelly Stem Cells (WJSCs) having similar properties to adult mesenchymal stem cells and thus representing a rich source of primitive cells to be potentially used in regenerative medicine. The aim of the present work was to investigate molecular changes that occur in WJSCs proteome in different experimental conditions: fresh primary cell culture and frozen cell. To analyze changes in protein expression of WJSCs undergoing different culturing procedures, we performed a comparative proteomic analysis (2DE followed by MALDI-TOF MS/MS nanoESI-Q-TOF MS coupled with nanoLC) between WJSCs from fresh and frozen cell culturing, respectively. Frozen WJSCs showed qualitative and quantitative changes compared to cells from fresh preparation, expressing proteins involved in replication, cellular defence mechanism and metabolism, that could ensure freeze-thaw survival. The results of this study could play a key role in elucidating possible mechanisms related to maintaining active proliferation and maximal cellular plasticity and thus making the use of WJSCs in cell therapy safe following bio-banking.


Assuntos
Criopreservação , Células-Tronco Mesenquimais , Proteoma/metabolismo , Adipogenia , Antígenos CD/metabolismo , Separação Celular , Células Cultivadas , Humanos , Osteogênese , Mapas de Interação de Proteínas , Telômero/genética , Cordão Umbilical/citologia
2.
Rev. colomb. radiol ; 25(1): 3905-3907, 2014. graf, tab
Artigo em Espanhol | LILACS, COLNAL | ID: biblio-995291

RESUMO

El neumotórax espontáneo primario bilateral simultáneo es una entidad poco frecuente que representa el 1,3% de los neumotórax espontáneos. La mayoría de los neumotórax espontáneos bilaterales se consideran secundarios. Se ha descrito en la literatura un número limitado de casos de neumotórax espontáneo bilateral de naturaleza primaria. Se presenta el caso de un paciente con neumotórax espontáneo primario bilateral, con una revisión de la función de las imágenes diagnósticas en este escenario clínico.


Simultaneous Bilateral Primary Spontaneous Pneumothorax is a very rate condition, representing 1.3% of all spontaneous pneumothoraces. Most bilateral spontaneous pneumothoraces are considered secondary. Very limited cases of bilateral spontaneous pneumothoraces of a primary nature have been described in literature. We present a case of a patient with bilateral primary spontaneous pneumothorax, reviewing the sequence of diagnostic images of this clinical scenario.


Assuntos
Humanos , Pneumotórax , Radiografia Torácica , Pulmão
3.
Adv Exp Med Biol ; 756: 349-53, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-22836653

RESUMO

We present a proteomic analysis of the rat carotid body (CB) preparation by comparison between normoxia and hypoxia. Proteomic investigation would be helpful to identify the stress-induced protein during hypoxia and to know what O(2) species are being sensed by CB cells. Adult Wistar rats were used, one group was kept in room air (21% O(2)) as control, and the other was kept in a Plexiglas chamber for 12 days in chronic hypoxia (10-11% inspired oxygen). A total protein extract for each lysated tissue was separated using a broad pH range no-linear IPG strip (3-10) and the second dimension was performed on a 9-16% polyacrylamide gel. Exposure to hypoxia for 12 days produced significant changes in protein expression, providing an initial insight into the mechanism underlying differences in susceptibility to hypoxia. Further investigation is needed to have an overview of the specific set of proteins present in the CB and the functions of such proteins in signal transduction and adaptation during hypoxia.


Assuntos
Corpo Carotídeo/metabolismo , Hipóxia/metabolismo , Proteoma/análise , Animais , Expressão Gênica , Mitocôndrias/metabolismo , Oxigênio/metabolismo , Ratos , Ratos Wistar , Espécies Reativas de Oxigênio/metabolismo , Transdução de Sinais
4.
Int J Immunopathol Pharmacol ; 17(2): 171-80, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-15171818

RESUMO

Ulcerative colitis (UC) is a chronic inflammatory disease of unknown aetiology and pathogenesis. The presence in the colonic mucosa of reactive cells expressing proinflammatory cytokines and chemokines is associated with high levels of IL-10, an anti-inflammatory cytokine. Our aim was to investigate the role of IL-10 and the beta chemokine LEC/CCL16 selectively up-regulated by IL-10 in inflammatory cell recruitment and cytokine and chemokine production during UC. We studied histologically, immunohistochemically and ultrastructurally colonic biopsies from 20 active UC patients and 10 control specimens taken far from any macroscopically detectable lesion in age and sex-matched patients with noninflammatory bowel disease. In active UC, immature dendritic cells (DCs) in the LP are associated with IL-10 in the T cell rich area. Furthermore, most of the LP-infiltrating macrophages strongly expressed LEC/CCL16, a chemokine upregulated by IL-10. To evaluate if LEC/CCL16 plays a role in the inflammatory reaction present in UC, we performed morphological studies in mice injected s.c. with syngeneic tumor cells engineered to produce LEC/CCL16. We found that the LEC protein locally released by LEC-gene-transfected tumor cells is a potent proinflammatory chemokine that induces the recruitment of a reactive infiltrate, and an angiogenic process mirroring that in human UC.


Assuntos
Quimiocinas CC/biossíntese , Colite Ulcerativa/metabolismo , Animais , Divisão Celular/fisiologia , Linhagem Celular Tumoral , Células Clonais , Colite Ulcerativa/patologia , Ensaio de Imunoadsorção Enzimática , Feminino , Imuno-Histoquímica , Interleucina-10/biossíntese , Mucosa Intestinal/patologia , Mucosa Intestinal/ultraestrutura , Camundongos , Camundongos Endogâmicos BALB C , Microscopia Eletrônica , RNA Mensageiro/biossíntese , Transfecção , Regulação para Cima/fisiologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...