کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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6280421 | 1615095 | 2015 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Research paperEvidence suggesting phosphodiesterase-3B regulation of NPY/AgRP gene expression in mHypoE-46 hypothalamic neurons Research paperEvidence suggesting phosphodiesterase-3B regulation of NPY/AgRP gene expression in mHypoE-46 hypothalamic neurons](/preview/png/6280421.png)
- PDE3B is expressed in hypothalamic NPY/AgRP neurons that play a key role in energy homeostasis.
- PDE3B is expressed in mHypoE-46 hypothalamic neuronal cells expressing NPY and AgRP.
- PDE3B overexpression decreased NPY/AgRP gene expression in mHypoE-46 cells.
- PDE3B knockdown increased NPY and AgRP gene expression in mHypoE-46 cells.
- This study shows PDE3B regulation of NPY/AgRP gene expression in mHypoE-46 cells.
Hypothalamic neurons expressing neuropeptide Y (NPY) and agouti related-protein (AgRP) are critical regulators of feeding behavior and body weight, and transduce the action of many peripheral signals including leptin and insulin. However, intracellular signaling molecules involved in regulating NPY/AgRP neuronal activity are incompletely understood. Since phosphodiesterase-3B (PDE3B) mediates the hypothalamic action of leptin and insulin on feeding, and is expressed in NPY/AgRP neurons, PDE3B could play a significant role in regulating NPY/AgRP neuronal activity. To investigate the direct regulation of NPY/AgRP neuronal activity by PDE3B, we examined the effects of gain-of-function or reduced function of PDE3B on NPY/AgRP gene expression in a clonal hypothalamic neuronal cell line, mHypoE-46, which endogenously express NPY, AgRP and PDE3B. Overexpression of PDE3B in mHypoE-46 cells with transfection of pcDNA-3.1-PDE3B expression plasmid significantly decreased NPY and AgRP mRNA levels and p-CREB levels as compared to the control plasmid. For the PDE3B knockdown study, mHypoE-46 cells transfected with lentiviral PDE3BshRNAmir plasmid or non-silencing lentiviral shRNAmir control plasmid were selected with puromycin, and stably transfected cells were grown in culture for 48Â h. Results showed that PDE3BshRNAmir mediated knockdown of PDE3B mRNA and protein levels (â¼60-70%) caused an increase in both NPY and AgRP gene expression and in p-CREB levels. Together, these results demonstrate a reciprocal change in NPY and AgRP gene expression following overexpression and knockdown of PDE3B, and suggest a significant role for PDE3B in the regulation of NPY/AgRP gene expression in mHypoE-46 hypothalamic neurons.
Journal: Neuroscience Letters - Volume 604, 14 September 2015, Pages 113-118