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Retraction Open Access | 10.1172/jci.insight.148169

Platelet IP6K1 regulates neutrophil extracellular trap–microparticle complex formation in acute pancreatitis

Raeh Madhi, Milladur Rahman, Dler Taha, Johan Linders, Mohammed Merza, Yongzhi Wang, Matthias Mörgelon, and Henrik Thorlacius

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Published February 22, 2021 - More info

Published in Volume 6, Issue 4 on February 22, 2021
JCI Insight. 2021;6(4):e148169. https://doi.org/10.1172/jci.insight.148169.
© 2021 pancreatitis et al. This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Published February 22, 2021 - Version history
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Related article:

Platelet IP6K1 regulates neutrophil extracellular trap-microparticle complex formation in acute pancreatitis
Raed Madhi, … , Matthias Mörgelin, Henrik Thorlacius
Raed Madhi, … , Matthias Mörgelin, Henrik Thorlacius
Research In-Press Preview Gastroenterology Inflammation

Platelet IP6K1 regulates neutrophil extracellular trap-microparticle complex formation in acute pancreatitis

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Abstract

Platelet inositol hexakisphosphate kinase 1 (IP6K1) has been shown to control systemic inflammation. Herein, we examined if platelets and IP6K1 regulate pancreatic tissue injury via formation of NETs in experimental models of acute pancreatitis (AP) in mice. By use of electron microscopy abundant NET formation was observed in the inflamed pancreas. These NETs contained numerous microparticles (MP) expressing CD41 or Mac-1. Platelet depletion reduced deposition of NET-MP complexes in the inflamed pancreas. Circulating platelet-neutrophil aggregates (PNA) were increased and inhibition of P-selectin not only disrupted PNA formation but also reduced NETs formation in the inflamed pancreas. NETs depleted of MPs had lower capacity to provoke amylase secretion and STAT-3 phosphorylation in acinar cells. Taurocholate-induced NETs formation, inflammation and tissue damage in the pancreas were decreased in IP6K1-deficient mice. Thrombin stimulation of mixtures of wild-type platelets and neutrophils resulted in NETs formation but not when IP6K1-deficient platelets were incubated with wild-type neutrophils. Polyphosphate rescue restored thrombin-induced NET formation in mixtures of IP6K1-deficient platelets and wild-type neutrophils. Platelet IP6K1 regulates NET-MP complex formation in the pancreas of mice during induction of AP. Targeting platelet IP6K1 might useful to decrease NET-dependent pancreatic tissue inflammation and tissue injury in patients with AP.

Authors

Raed Madhi, Milladur Rahman, Dler Taha, Johan Linders, Mohammed Merza, Yongzhi Wang, Matthias Mörgelin, Henrik Thorlacius

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Original citation: JCI Insight. 2019;e129270. https://doi.org/10.1172/jci.insight.129270

Citation for this retraction: JCI Insight. 2021;6(4):e148169. https://doi.org/10.1172/jci.insight.148169

Following a review by the Swedish National Board for Assessment of Research Misconduct, it was determined that a serious breach of good scientific practice in the form of falsification occurred during the pseudocoloring of scanning electron micrographs in this article. The National Board determined that the serious deviation from good research practice was not intentionally committed and concluded that no research misconduct occurred. The paper is being retracted because JCI Insight editorial policy prohibits falsification and misrepresentation of data.

Footnotes

See the related article at Platelet IP6K1 regulates neutrophil extracellular trap–microparticle complex formation in acute pancreatitis.

Version history
  • Version 1 (February 22, 2021): Electronic publication
  • Version 2 (March 10, 2021): The original citation date was corrected.

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