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Extracellular matrix expression in human pancreatic fat cells of patients with normal glucose regulation, prediabetes and type 2 diabetes.

Int. J. Mol. Sci. 24:18 (2023)
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Previously, we found that human pancreatic preadipocytes (PPAs) and islets influence each other and that the crosstalk with the fatty liver via the hepatokine fetuin-A/palmitate induces inflammatory responses. Here, we examined whether the mRNA-expression of pancreatic extracellular matrix (ECM)-forming and -degrading components differ in PPAs from individuals with normal glucose regulation (PPAs-NGR), prediabetes (PPAs-PD), and type 2 diabetes (PPAs-T2D), and whether fetuin-A/palmitate impacts ECM-formation/degradation and associated monocyte invasion. Human pancreatic resections were analyzed (immuno)histologically. PPAs were studied for mRNA expression by real-time PCR and protein secretion by Luminex analysis. Furthermore, co-cultures with human islets and monocyte migration assays in Transwell plates were conducted. We found that in comparison with NGR-PPAs, TIMP-2 mRNA levels were lower in PPAs-PD, and TGF-β1 mRNA levels were higher in PPAs-T2D. Fetuin-A/palmitate reduced fibronectin, decorin, TIMP-1/-2 and TGF-ß1 mRNA levels. Only fibronectin was strongly downregulated by fetuin-A/palmitate independently of the glycemic status. Co-culturing of PPAs with islets increased TIMP-1 mRNA expression in islets. Fetuin-A/palmitate increased MMP-1, usherin and dermatopontin mRNA-levels in co-cultured islets. A transmigration assay showed increased monocyte migration towards PPAs, which was enhanced by fetuin-A/palmitate. This was more pronounced in PPAs-T2D. The expression of distinct ECM components differs in PPAs-PD and PPAs-T2D compared to PPAs-NGR, suggesting that ECM alterations can occur even in mild hyperglycemia. Fetuin-A/palmitate impacts on ECM formation/degradation in PPAs and co-cultured islets. Fetuin-A/palmitate also enhances monocyte migration, a process which might impact on matrix turnover.
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Publication type Article: Journal article
Document type Scientific Article
Keywords (pre)adipocytes ; Adipose Tissue ; Diabetes ; Extracellular Matrix ; Fetuin-a ; Islets ; Monocytes; Growth-factor-beta; Adipose-tissue; Dermatopontin Interacts; Adipocyte; Metalloproteinases; Inhibitors; Inflammation; Fibronectin; Macrophages; Integration
Language english
Publication Year 2023
HGF-reported in Year 2023
ISSN (print) / ISBN 1661-6596
e-ISSN 1422-0067
Quellenangaben Volume: 24, Issue: 13, Pages: , Article Number: 18 Supplement: ,
Publisher MDPI
Publishing Place Basel
Reviewing status Peer reviewed
POF-Topic(s) 90000 - German Center for Diabetes Research
Research field(s) Helmholtz Diabetes Center
PSP Element(s) G-502400-001
Grants Research (BMBF) to the German Center for Diabetes Re-search (DZD e.V.)
Scopus ID 85164844294
PubMed ID 37446346
Erfassungsdatum 2023-10-06