scholarly journals A subpopulation of itch‐sensing neurons marked by Ret and somatostatin expression

EMBO Reports ◽  
2016 ◽  
Vol 17 (4) ◽  
pp. 585-600 ◽  
Author(s):  
Kalina K Stantcheva ◽  
Loredana Iovino ◽  
Rahul Dhandapani ◽  
Concepcion Martinez ◽  
Laura Castaldi ◽  
...  
1996 ◽  
Vol 16 (24) ◽  
pp. 8140-8148 ◽  
Author(s):  
Elisabeth Pellegrini ◽  
Marie Thérèse Bluet-Pajot ◽  
Françoise Mounier ◽  
Pamela Bennett ◽  
Claude Kordon ◽  
...  

2020 ◽  
Vol 21 (11) ◽  
pp. 4170 ◽  
Author(s):  
Emmanuel Ampofo ◽  
Lisa Nalbach ◽  
Michael D. Menger ◽  
Matthias W. Laschke

Somatostatin is a peptide hormone, which most commonly is produced by endocrine cells and the central nervous system. In mammals, somatostatin originates from pre-prosomatostatin and is processed to a shorter form, i.e., somatostatin-14, and a longer form, i.e., somatostatin-28. The two peptides repress growth hormone secretion and are involved in the regulation of glucagon and insulin synthesis in the pancreas. In recent years, the processing and secretion of somatostatin have been studied intensively. However, little attention has been paid to the regulatory mechanisms that control its expression. This review provides an up-to-date overview of these mechanisms. In particular, it focuses on the role of enhancers and silencers within the promoter region as well as on the binding of modulatory transcription factors to these elements. Moreover, it addresses extracellular factors, which trigger key signaling pathways, leading to an enhanced somatostatin expression in health and disease.


1997 ◽  
Vol 68 (1) ◽  
pp. 15-21 ◽  
Author(s):  
Martin A Turman ◽  
M.Sue O'Dorisio ◽  
Thomas M O'Dorisio ◽  
Courtney A Apple ◽  
Anne R Albers

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Luise Doering ◽  
Rahul Khatri ◽  
Sebastian Friedrich Petry ◽  
Heinrich Sauer ◽  
Hans-Peter Howaldt ◽  
...  

Cell Reports ◽  
2020 ◽  
Vol 30 (6) ◽  
pp. 1995-2005.e5 ◽  
Author(s):  
Seungjoon Kim ◽  
Hyeonho Kim ◽  
Dongseok Park ◽  
Jinhu Kim ◽  
Joohyeon Hong ◽  
...  

1998 ◽  
Vol 10 (2) ◽  
pp. 99-111 ◽  
Author(s):  
Patrizia Corsi ◽  
Gianluigi Forloni ◽  
Michele Troia ◽  
Teresa Lettini ◽  
Joseph T. Coyle

2011 ◽  
Vol 343-344 ◽  
pp. 1248-1254
Author(s):  
Jing Hua Ding ◽  
Qian Yun Xi ◽  
Hong Yi Li ◽  
Gang Shu ◽  
Song Bo Wang ◽  
...  

Two shRNA sequences against porcine somatostatin (SST) were designed using software available on the NCBI website. The designed RNA sequences were chemically synthesized and cloned into lentiviral vectors (LV-siRNA1 and LV-siRNA2). Porcine somatostatin cDNA was amplified and cloned into pcDNA3.1 (pcDNA3.1-SST). LV-siRNA1 or LV-siRNA2 was cotransfected with pcDNA3.1-SST into NIH3T3 cells. Real-time RT-PCR for the detection of SST mRNA, revealed that LV-siRNA1 and LV-siRNA2 suppressed SST expression by 87.9% and 86.3% (P< 0.01), respectively. In addition, radioimmunoassay (RIA) for direct detection of SST indicated that the suppression ratios for LV-siRNA1 and LV-siRNA2 were 55.1% and 51.6% (P< 0.01), respectively. These data showed that the 2 shRNA sequences were effective in suppressing SST expression and may provide an approach to down-regulate bothin vitroandin vivoexpression of porcine SST.


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