Optical tools for understanding the complexity of beta-cell signalling and insulin release
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F18%3A00498654" target="_blank" >RIV/61388963:_____/18:00498654 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1038/s41574-018-0105-2" target="_blank" >http://dx.doi.org/10.1038/s41574-018-0105-2</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/s41574-018-0105-2" target="_blank" >10.1038/s41574-018-0105-2</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Optical tools for understanding the complexity of beta-cell signalling and insulin release
Popis výsledku v původním jazyce
Following stimulation, pancreatic beta-cells must orchestrate a plethora of signalling events to ensure the appropriate release of insulin and maintenance of normal glucose homeostasis. Failure at any point in this cascade leads to impaired insulin secretion, elevated blood levels of glucose and eventually type 2 diabetes mellitus. Likewise, beta-cell replacement or regeneration strategies for the treatment of both type 1 and type 2 diabetes mellitus might fail if the correct cell signalling phenotype cannot be faithfully recreated. However, current understanding of beta-cell function is complicated because of the highly dynamic nature of their intracellular and intercellular signalling as well as insulin release itself. beta-Cells must precisely integrate multiple signals stemming from multiple cues, often with differing intensities, frequencies and cellular and subcellular localizations, before converging these signals onto insulin exocytosis. In this respect, optical approaches with high resolution in space and time are extremely useful for properly deciphering the complexity of beta-cell signalling. An increased understanding of beta-cell signalling might identify new mechanisms underlying insulin release, with relevance for future drug therapy and de novo stem cell engineering of functional islets.
Název v anglickém jazyce
Optical tools for understanding the complexity of beta-cell signalling and insulin release
Popis výsledku anglicky
Following stimulation, pancreatic beta-cells must orchestrate a plethora of signalling events to ensure the appropriate release of insulin and maintenance of normal glucose homeostasis. Failure at any point in this cascade leads to impaired insulin secretion, elevated blood levels of glucose and eventually type 2 diabetes mellitus. Likewise, beta-cell replacement or regeneration strategies for the treatment of both type 1 and type 2 diabetes mellitus might fail if the correct cell signalling phenotype cannot be faithfully recreated. However, current understanding of beta-cell function is complicated because of the highly dynamic nature of their intracellular and intercellular signalling as well as insulin release itself. beta-Cells must precisely integrate multiple signals stemming from multiple cues, often with differing intensities, frequencies and cellular and subcellular localizations, before converging these signals onto insulin exocytosis. In this respect, optical approaches with high resolution in space and time are extremely useful for properly deciphering the complexity of beta-cell signalling. An increased understanding of beta-cell signalling might identify new mechanisms underlying insulin release, with relevance for future drug therapy and de novo stem cell engineering of functional islets.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10608 - Biochemistry and molecular biology
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Nature Reviews Endocrinology
ISSN
1759-5029
e-ISSN
—
Svazek periodika
14
Číslo periodika v rámci svazku
12
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
17
Strana od-do
721-737
Kód UT WoS článku
000449832300014
EID výsledku v databázi Scopus
2-s2.0-85055429349