Neutrophil-Associated Inflammatory Changes in the Pre-Diabetic Pancreas of Early-Age NOD Mice.
Age Factors
Animals
Animals, Newborn
Antigens, Ly
/ metabolism
Autoantibodies
/ metabolism
Citrullination
/ immunology
Extracellular Traps
/ immunology
Female
Growth and Development
/ physiology
Histones
/ metabolism
Inflammation
/ complications
Insulin-Secreting Cells
/ immunology
Leukocyte Elastase
/ metabolism
Male
Membrane Glycoproteins
/ metabolism
Mice
Mice, Inbred C57BL
Mice, Inbred NOD
Neutrophils
/ immunology
Pancreas
/ immunology
Prediabetic State
/ immunology
AZD5904
AZD9668
autoimmunity
myeloperoxidase
neutrophil elastase
neutrophils
non-obese diabetes (NOD) mice
type 1 diabetes
Journal
Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782
Informations de publication
Date de publication:
2021
2021
Historique:
received:
26
05
2020
accepted:
01
02
2021
entrez:
29
3
2021
pubmed:
30
3
2021
medline:
22
12
2021
Statut:
epublish
Résumé
A growing body of evidence indicates that neutrophils are the first major leukocyte population accumulating inside the pancreas even before the onset of a lymphocytic-driven impairment of functional beta cells in type 1 diabetes mellitus (T1D). In humans, pancreata from T1D deceased donors exhibit significant neutrophil accumulation. We present a time course of previously unknown inflammatory changes that accompany neutrophil and neutrophil elastase accumulation in the pancreas of the non-obese diabetic (NOD) mouse strain as early as 2 weeks of age. We confirm earlier findings in NOD mice that neutrophils accumulate as early as 2 weeks of age. We also observe a concurrent increase in the expression of neutrophil elastase in this time period. We also detect components of neutrophil extracellular traps (NET) mainly in the exocrine tissue of the pancreas during this time as well as markers of vascular pathology as early as 2 weeks of age. Age- and sex-matched C57BL/6 mice do not exhibit these features inside the pancreas. When we treated NOD mice with inhibitors of myeloperoxidase and neutrophil elastase, two key effectors of activated neutrophil activity, alone or in combination, we were unable to prevent the progression to hyperglycemia in any manner different from untreated control mice. Our data confirm and add to the body of evidence demonstrating neutrophil accumulation inside the pancreas of mice genetically susceptible to T1D and also offer novel insights into additional pathologic mechanisms involving the pancreatic vasculature that have, until now, not been discovered inside the pancreata of these mice. However, inhibition of key neutrophil enzymes expressed in activated neutrophils could not prevent diabetes. These findings add to the body of data supporting a role for neutrophils in the establishment of early pathology inside the pancreas, independently of, and earlier from the time at onset of lymphocytic infiltration. However, they also suggest that inhibition of neutrophils alone, acting
Identifiants
pubmed: 33776903
doi: 10.3389/fendo.2021.565981
pmc: PMC7988208
doi:
Substances chimiques
Antigens, Ly
0
Autoantibodies
0
Histones
0
Ly6G antigen, mouse
0
Membrane Glycoproteins
0
P-selectin ligand protein
0
Leukocyte Elastase
EC 3.4.21.37
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
565981Subventions
Organisme : NCATS NIH HHS
ID : R21 TR001728
Pays : United States
Informations de copyright
Copyright © 2021 Garciafigueroa, Phillips, Engman, Trucco and Giannoukakis.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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