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Fumarate Hydratase Deletion in Pancreatic beta Cells Leads to Progressive Diabetes

Adam, J. (author)
Ramracheya, R. (author)
Chibalina, M. V. (author)
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Ternette, N. (author)
Hamilton, A. (author)
Tarasov, A. I. (author)
Zhang, Q. (author)
Rebelato, E. (author)
Rorsman, N. J. G. (author)
Martin-del-Rio, R. (author)
Lewis, A. (author)
Ozkan, G. (author)
Do, H. W. (author)
Spegel, P. (author)
Saitoh, K. (author)
Kato, K. (author)
Igarashi, K. (author)
Kessler, B. M. (author)
Pugh, C. W. (author)
Tamarit-Rodriguez, J. (author)
Mulder, H. (author)
Clark, A. (author)
Frizzell, N. (author)
Soga, T. (author)
Ashcroft, Frances M. (author)
Silver, A. (author)
Pollard, Patrick (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
Rorsman, Patrik, 1959 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
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 (creator_code:org_t)
Elsevier BV, 2017
2017
English.
In: Cell Reports. - : Elsevier BV. - 2211-1247. ; 20:13, s. 3135-3148
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We explored the role of the Krebs cycle enzyme fumarate hydratase (FH) in glucose-stimulated insulin secretion (GSIS). Mice lacking Fh1 in pancreatic beta cells (Fh1 beta KO mice) appear normal for 6-8 weeks but then develop progressive glucose intolerance and diabetes. Glucose tolerance is rescued by expression of mitochondrial or cytosolic FH but not by deletion of Hif1 alpha or Nrf2. Progressive hyperglycemia in Fh1bKO mice led to dysregulated metabolism in b cells, a decrease in glucose-induced ATP production, electrical activity, cytoplasmic [Ca2+](i) elevation, and GSIS. Fh1 loss resulted in elevated intracellular fumarate, promoting succination of critical cysteines in GAPDH, GMPR, and PARK 7/DJ-1 and cytoplasmic acidification. Intracellular fumarate levels were increased in islets exposed to high glucose and in islets from human donors with type 2 diabetes (T2D). The impaired GSIS in islets from diabetic Fh1bKO mice was ameliorated after culture under normoglycemic conditions. These studies highlight the role of FH and dysregulated mitochondrial metabolism in T2D.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Fysiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Physiology (hsv//eng)

Keyword

insulin-secretion
mitochondrial stress
chemical-modification
glucose-homeostasis
metabolism
dehydrogenase
succination
biomarker
pathway
islets
Cell Biology

Publication and Content Type

ref (subject category)
art (subject category)

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