assessing the levels of camp response element binding protein1 (creb1) after sirna mediated knockdown in k562 cells
Authors
abstract
objective: creb1 is an important downstream protein for many signaling pathways. by designing efficient sirnas against creb1, it may be possible to assess the role of molecules involved in signaling pathways in different cell types. in this research the efficiency of creb1 knockdown by two different sirnas in k562 cells has been studied. materials and methods: sirnas have been designed according to the criteria suggested by reynolds et al. k562 cells were transfected by sirna using lipofectamine 2000. the efficiency of creb knockdown has been assessed by quantitative relative real-time pcr. results: our results have shown that only one of the sirnas has a high level of inhibitory effect on creb1 gene expression. the expression of creb1 by this sirna was knocked-down by 87% in k562 cells. conclusion: in this research, although two sirnas were designed according to the reynolds et al. criteria, only one showed an inhibitory effect. reasons other than the aforementioned criteria may be involved in effectiveness of sirnas.
similar resources
مهار ژن camp response element binding protein توسط sirna در رده سلولی k۵۶۲
هدف: پروتئین creb یک فاکتور مهم پایین دست بسیاری از مسیرهای علامتی به شمار می رود. با طراحی sirna کارامد برای ژن creb می توان مسیرهای علامتی بسیاری از داروها را در سلول های مختلف به ویژه سلول k562 بررسی نمود. در این تحقیق میزان مهار بیان ژن creb با به کارگیری دو sirna مختلف برای این ژن بررسی شد. مواد و روش ها: طراحی sirna براساس معیار reynolds انجام گرفت. سلول های k562 با روش لیپوفکشن با sirna ...
full text[cAMP response-element binding protein participates in the phosphorylated extracellular signal-regulate kinase mediated neuropathic pain].
It has been reported that extracellular signal-regulate kinase (ERK) is involved in the modulation of nociceptive information and central sensitization produced by intense noxious stimuli and/or peripheral tissue inflammation. Few studies have explored the relationship between ERK and cAMP response-element binding protein (CREB) in neuropathic pain after nerve injury, such as chronic constricti...
full textcAMP response element-binding protein-mediated gene expression increases the intrinsic excitability of CA1 pyramidal neurons.
To investigate the role of CREB-mediated gene expression on the excitability of CA1 pyramidal neurons, we obtained intracellular recordings from pyramidal neurons of transgenic mice expressing a constitutively active form of CREB, VP16-CREB, in a regulated and restricted manner. We found that transgene expression increased the neuronal excitability and inhibited the slow and medium afterhyperpo...
full textAntisense oligodeoxynucleotide-mediated disruption of hippocampal cAMP response element binding protein levels impairs consolidation of memory for water maze training.
Extensive evidence suggests that long term memory (LTM) formation is dependent on the activation of neuronal second messenger systems and requires protein synthesis. The cAMP response element binding protein (CREB) is a constitutively expressed regulatory transcription factor that couples changes in second messenger levels to changes in cellular transcription. Several recent studies suggest tha...
full textRole of cAMP Response Element Binding Protein in Cardiovascular Remodeling
The cAMP response element binding protein (CREB) is a ubiquitously expressed nuclear transcription factor that is activated by various extracellular stimuli. CREB is known to regulate the expression of genes important to cell proliferation, differentiation, adaptation, and survival in many cell types. Loss of CREB function by transgenic overexpression of dominant negative CREB or targeted delet...
full textRescue of impaired long-term facilitation at sensorimotor synapses of Aplysia following siRNA knockdown of CREB1.
Memory impairment is often associated with disrupted regulation of gene induction. For example, deficits in cAMP response element-binding protein (CREB) binding protein (CBP; an essential cofactor for activation of transcription by CREB) impair long-term synaptic plasticity and memory. Previously, we showed that small interfering RNA (siRNA)-induced knockdown of CBP in individual sensory neuron...
full textMy Resources
Save resource for easier access later
Journal title:
modares journal of medical sciences: pathobiologyPublisher: tarbiat modares university
ISSN 1562-9554
volume 11
issue Autumn 2008 & Winter 2009 2009
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023