Faculty Opinions recommendation of The vascular basement membrane: a niche for insulin gene expression and Beta cell proliferation.

Author(s):  
Victoria Prince
2006 ◽  
Vol 10 (3) ◽  
pp. 397-405 ◽  
Author(s):  
Ganka Nikolova ◽  
Normund Jabs ◽  
Irena Konstantinova ◽  
Anna Domogatskaya ◽  
Karl Tryggvason ◽  
...  

2010 ◽  
Vol 285 (44) ◽  
pp. 33623-33631 ◽  
Author(s):  
Nadeeja Wijesekara ◽  
Mansa Krishnamurthy ◽  
Alpana Bhattacharjee ◽  
Aamir Suhail ◽  
Gary Sweeney ◽  
...  

Diabetologia ◽  
2012 ◽  
Vol 55 (5) ◽  
pp. 1390-1399 ◽  
Author(s):  
J. Lau ◽  
J. Svensson ◽  
L. Grapensparr ◽  
Å. Johansson ◽  
P.-O. Carlsson

2020 ◽  
Author(s):  
H. Medini ◽  
T. Cohen ◽  
D. Mishmar

AbstractMitochondrial gene expression is pivotal to cell metabolism. Nevertheless, it is unknown whether it diverges within a given cell type. Here, we analysed single-cell RNA-seq experiments from ∼4600 human pancreatic alpha and beta cells, as well as ∼900 mouse beta cells. Cluster analysis revealed two distinct human beta cells populations, which diverged by mitochondrial (mtDNA) and nuclear DNA (nDNA)-encoded oxidative phosphorylation (OXPHOS) gene expression in healthy and diabetic individuals, and in newborn but not in adult mice. Insulin gene expression was elevated in beta cells with higher mtDNA gene expression in humans and in young mice. Such human beta cell populations also diverged in mt-RNA mutational repertoire, and in their selective signature, thus implying the existence of two previously overlooked distinct and conserved beta cell populations. While applying our approach to alpha cells, two sub-populations of cells were identified which diverged in mtDNA gene expression, yet these cellular populations did not consistently diverge in nDNA OXPHOS genes expression, nor did they correlate with the expression of glucagon, the hallmark of alpha cells. Thus, pancreatic beta cells within an individual are divided into distinct groups with unique metabolic-mitochondrial signature.


2014 ◽  
Vol 46 ◽  
pp. 350
Author(s):  
Travis Parkulo ◽  
Dale Riggs ◽  
Barbara Jackson ◽  
Stanley Zaslau ◽  
Evan DeVallance ◽  
...  

Diabetologia ◽  
2014 ◽  
Vol 57 (8) ◽  
pp. 1645-1654 ◽  
Author(s):  
Dominika Nackiewicz ◽  
Meixia Dan ◽  
Wei He ◽  
Rosa Kim ◽  
Anisa Salmi ◽  
...  

2000 ◽  
Vol 164 (3) ◽  
pp. 277-286 ◽  
Author(s):  
A Petryk ◽  
D Fleenor ◽  
P Driscoll ◽  
M Freemark

Previous studies have shown that lactogenic hormones stimulate beta-cell proliferation and insulin production in pancreatic islets. However, all such studies have been conducted in cells incubated in medium containing glucose. Since glucose independently stimulates beta-cell replication and insulin production, it is unclear whether the effects of prolactin (PRL) on insulin gene expression are exerted directly or through the uptake and/or metabolism of glucose. We examined the interactions between glucose and PRL in the regulation of insulin gene transcription and the expression of glucose transporter-2 (glut-2) and glucokinase mRNAs in rat insulinoma (INS-1) cells. In the presence of 5.5 mM glucose, the levels of preproinsulin and glut-2 mRNAs in PRL-treated cells exceeded the levels in control cells (1.7-fold, P<0.05 and 2-fold, P<0.05 respectively). The maximal effects of PRL were noted at 24-48 h of incubation. PRL had no effect on the levels of glucokinase mRNA. The higher levels of glut-2 mRNA were accompanied by an increase in the number of cellular glucose transporters, as demonstrated by a 1. 4- to 2.4-fold increase in the uptake of 2-deoxy-d-[(3)H]glucose in PRL-treated INS-1 cells (P<0.001). These findings suggested that the insulinotropic effect of PRL is mediated, in part, by induction of glucose transport and/or glucose metabolism. Nevertheless, even in the absence of glucose, PRL stimulated increases in the levels of preproinsulin mRNA (3.4-fold higher than controls, P<0.0001) and glut-2 mRNA (2-fold higher than controls, P<0.01). These observations suggested that PRL exerts glucose-independent as well as glucose-dependent effects on insulin gene expression. Support for this hypothesis was provided by studies of insulin gene transcription using INS-1 cells transfected with a plasmid containing the rat insulin 1 promoter linked to a luciferase reporter gene. Glucose and PRL, alone and in combination, stimulated increases in cellular luciferase activity. The relative potencies of glucose (5.5 mM) alone, PRL alone, and glucose plus PRL in combination were 2.2 (P<0.001), 3.4 (P<0.01), and 7.9 (P<0.0001) respectively. Our findings suggest that glucose and PRL act synergistically to induce insulin gene transcription.


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