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1.
Noncoding RNA Res ; 2(1): 74-82, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30159423

RESUMEN

In mammals, short (mi-) and long non-coding (lnc) RNAs are immensely abundant and they are proving to be more functional than ever before. Particularly in cell reprogramming, non-coding RNAs are essential to establish the pluripotent network and are indispensable to reprogram somatic cells to pluripotency. Through systematic screening and mechanistic studies, diverse functional features of both miRNA and lncRNAs have emerged as either scaffolds, inhibitors, or co-activators, necessary to orchestrate the intricacy of gene regulation. Furthermore, the collective characterizations of both miRNA and lncRNA reveal their interdependency (e.g. sequestering the function of the other) to modulate cell reprogramming. This review broadly explores the regulatory processes of cell reprogramming - with key functional examples in neuronal and cardiac differentiations - in the context of both short and long non-coding RNAs.

2.
Tissue Eng Part C Methods ; 18(11): 890-902, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-22889128

RESUMEN

Endothelial progenitor cells (EPCs) play a significant role in multiple biological processes such as vascular homeostasis, regeneration, and tumor angiogenesis. This makes them a promising cell of choice for studying a variety of biological processes, toxicity assays, biomaterial-cell interaction studies, as well as in tissue-engineering applications. In this study, we report the generation of two clones of SV40-immortalized EPCs from umbilical cord blood. These cells retained most of the functional features of mature endothelial cells and showed no indication of senescence after repeated culture for more than 240 days. Extensive functional characterization of the immortalized cells by western blot, flow cytometry, and immunofluorescence studies substantiated that these cells retained their ability to synthesize nitric oxide, von Willebrand factor, P-Selectin etc. These cells achieved unlimited proliferation potential subsequent to inactivation of the cyclin-dependent kinase inhibitor p21, but failed to form colonies on soft agar. We also show their enhanced growth and survival on vascular biomaterials compared to parental cultures in late population doubling. These immortalized EPCs can be used as a cellular model system for studying the biology of these cells, gene manipulation experiments, cell-biomaterial interactions, as well as a variety of tissue-engineering applications.


Asunto(s)
Prótesis Vascular , Células Endoteliales/citología , Sangre Fetal/citología , Células Madre/citología , Ingeniería de Tejidos/métodos , Antígenos Transformadores de Poliomavirus/metabolismo , Adhesión Celular , Ciclo Celular , Línea Celular Transformada , Proliferación Celular , Separación Celular , Senescencia Celular , Células Endoteliales/metabolismo , Células Endoteliales de la Vena Umbilical Humana/citología , Humanos , Cinética , Células Madre/metabolismo
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