SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Idevall Hagren Olof 1980 )
 

Sökning: WFRF:(Idevall Hagren Olof 1980 ) > cAMP Mediators of P...

cAMP Mediators of Pulsatile Insulin Secretion from Glucose-stimulated Single β-Cells

Idevall Hagren, Olof, 1980- (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi,Anders Tengholm
Barg, Sebastian (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi
Gylfe, Erik (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi
visa fler...
Tengholm, Anders (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi
visa färre...
 (creator_code:org_t)
2010
2010
Engelska.
Ingår i: Journal of Biological Chemistry. - 0021-9258 .- 1083-351X. ; 285:30, s. 23005-23016
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Pulsatile insulin release from glucose-stimulated beta-cells is driven by oscillations of the Ca2+ and cAMP concentrations in the subplasma membrane space ([Ca2+](pm) and [cAMP](pm)). To clarify mechanisms by which cAMP regulates insulin secretion, we performed parallel evanescent wave fluorescence imaging of [cAMP](pm), [Ca2+](pm), and phosphatidylinositol 3,4,5-trisphosphate (PIP3) in the plasma membrane. This lipid is formed by autocrine insulin receptor activation and was used to monitor insulin release kinetics from single MIN6 beta-cells. Elevation of the glucose concentration from 3 to 11 mM induced, after a 2.7-min delay, coordinated oscillations of [Ca2+](pm), [cAMP](pm), and PIP3. Inhibitors of protein kinase A (PKA) markedly diminished the PIP3 response when applied before glucose stimulation, but did not affect already manifested PIP3 oscillations. The reduced PIP3 response could be attributed to accelerated depolarization causing early rise of [Ca2+](pm) that preceded the elevation of [cAMP](pm). However, the amplitude of the PIP3 response after PKA inhibition was restored by a specific agonist to the cAMP-dependent guanine nucleotide exchange factor Epac. Suppression of cAMP formation with adenylyl cyclase inhibitors reduced already established PIP3 oscillations in glucose-stimulated cells, and this effect was almost completely counteracted by the Epac agonist. In cells treated with small interfering RNA targeting Epac2, the amplitudes of the glucose-induced PIP3 oscillations were reduced, and the Epac agonist was without effect. The data indicate that temporal coordination of the triggering [Ca2+](pm) and amplifying [cAMP](pm) signals is important for glucose-induced pulsatile insulin release. Although both PKA and Epac2 partake in initiating insulin secretion, the cAMP dependence of established pulsatility is mediated by Epac2.

Ämnesord

NATURVETENSKAP  -- Biologi -- Cellbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Cell Biology (hsv//eng)

Nyckelord

cAMP
Ca2
insulin
PKA
Epac
Evanescent wave microscopy
beta cell
oscillations
Cell biology
Cellbiologi
Molekylär cellbiologi
Molecular Cellbiology

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Hitta mer i SwePub

Av författaren/redakt...
Idevall Hagren, ...
Barg, Sebastian
Gylfe, Erik
Tengholm, Anders
Om ämnet
NATURVETENSKAP
NATURVETENSKAP
och Biologi
och Cellbiologi
Artiklar i publikationen
Journal of Biolo ...
Av lärosätet
Uppsala universitet

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy