Platelet‐derived lipids promote insulin secretion of pancreatic β cells

Abstract: Hyperreactive platelets are commonly observed in diabetic patients indicating a potential link between glucose homeostasis and platelet reactivity. This raises the possibility that platelets may play a role in the regulation of metabolism. Pancreatic β cells are the central regulators of systemic glucose homeostasis. Here, we show that factor (s) derived from β cells stimulate platelet activity and platelets selectively localize to the vascular endothelium of pancreatic islets. Both depletion of platelets and ablation of major platelet adhesion or activation pathways consistently resulted in impaired glucose tolerance and decreased circulating insulin levels. Furthermore, we found platelet‐derived lipid classes to promote insulin secretion and identified 20‐Hydroxyeicosatetraenoic acid (20‐HETE) as the main factor promoting β cells function. Finally, we demonstrate that the levels of platelet‐derived 20‐HETE decline with age and that this parallels with reduced impact of platelets on β cell function. Our findings identify an unexpected function of platelets in the regulation of insulin secretion and glucose metabolism, which promotes metabolic fitness in young individuals.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Platelet‐derived lipids promote insulin secretion of pancreatic β cells ; day:25 ; month:07 ; year:2023 ; extent:23
EMBO molecular medicine / European Molecular Biology Organization ; (25.07.2023) (gesamt 23)

Urheber
Karwen, Till
Kolczynska‐Matysiak, Katarzyna
Gross, Carina
Löffler, Mona Christina
Friedrich, Mike
Loza‐Valdes, Angel
Schmitz, Werner
Wit, Magdalena
Dziaczkowski, Filip
Belykh, Andrei
Trujillo‐Viera, Jonathan
El‐Merahbi, Rabih
Deppermann, Carsten
Nawaz, Sameena
Hastoy, Benoit
Demczuk, Agnieszka
Erk, Manuela
Wieckowski, Mariusz R.
Rorsman, Patrik
Heinze, Katrin G.
Stegner, David
Nieswandt, Bernhard
Sumara, Grzegorz

DOI
10.15252/emmm.202216858
URN
urn:nbn:de:101:1-2023072615010761702741
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:54 MESZ

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Beteiligte

  • Karwen, Till
  • Kolczynska‐Matysiak, Katarzyna
  • Gross, Carina
  • Löffler, Mona Christina
  • Friedrich, Mike
  • Loza‐Valdes, Angel
  • Schmitz, Werner
  • Wit, Magdalena
  • Dziaczkowski, Filip
  • Belykh, Andrei
  • Trujillo‐Viera, Jonathan
  • El‐Merahbi, Rabih
  • Deppermann, Carsten
  • Nawaz, Sameena
  • Hastoy, Benoit
  • Demczuk, Agnieszka
  • Erk, Manuela
  • Wieckowski, Mariusz R.
  • Rorsman, Patrik
  • Heinze, Katrin G.
  • Stegner, David
  • Nieswandt, Bernhard
  • Sumara, Grzegorz

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