Obesity Induced by High-Fat Diet Is Associated With Critical Changes in Biological and Molecular Functions of Mesenchymal Stromal Cells Present in Visceral Adipose Tissue

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Abstract

The mesenchymal stromal cells (MSCs) residing within the stromal component of visceral adipose tissue appear to be greatly affected by obesity, with impairment of their functions and presence of senescence. To gain further insight into these phenomena, we analyzed the changes in total proteome content and secretome of mouse MSCs after a high-fat diet (HFD) treatment compared to a normal diet (ND). In healthy conditions, MSCs are endowed with functions mainly devoted to vesicle trafficking. These cells have an immunoregulatory role, affecting leukocyte activation and migration, acute inflammation phase response, chemokine signaling, and platelet activities. They also present a robust response to stress. We identified four signaling pathways (TGF-β, VEGFR2, HMGB1, and Leptin) that appear to govern the cells’ functions. In the obese mice, MSCs showed a change in their functions. The immunoregulation shifted toward pro-inflammatory tasks with the activation of interleukin-1 pathway and of Granzyme A signaling. Moreover, the methionine degradation pathway and the processing of capped intronless pre-mRNAs may be related to the inflammation process. The signaling pathways we identified in ND MSCs were replaced by MET, WNT, and FGFR2 signal transduction, which may play a role in promoting inflammation, cancer, and aging © 2024 Elsevier B.V., All rights reserved.

Description

Acar, Mustafa Burak/0000-0002-9109-6575; Ayaz Guner, Serife/0000-0002-1052-0961; Murat-Cifci, Aysegul/0000-0002-6823-4175; Guner, Huseyin/0000-0002-0220-5224; Ozcan, Servet/0000-0002-9914-8843; Di Bernardo, Giovanni/0000-0002-4985-4029;

Keywords

Mesenchymal Stromal Cells, Senescence, Visceral Adipose Tissue, Methionine, Granzymes, Hmgb1 Protein, Interleukin-1, Leptin, Methionine, Proteome, Proto-Oncogene Proteins C-Met, Receptor, Fibroblast Growth Factor, Type 2, Rna Precursors, Transforming Growth Factor Beta, Vascular Endothelial Growth Factor Receptor-2, Fibroblast Growth Factor Receptor 2, Granzyme, High Mobility Group B1 Protein, Interleukin 1, Leptin, Methionine, Proteome, Rna Precursor, Scatter Factor Receptor, Transforming Growth Factor Beta, Vasculotropin Receptor 2, Aging, Animal, Cytology, Inflammation, Intra-Abdominal Fat, Lipid Diet, Mesenchymal Stem Cell, Metabolism, Mouse, Obesity, Rna Processing, Secretory Vesicle, Signal Transduction, Wnt Signaling, Aging, Animals, Diet, High-Fat, Granzymes, Hmgb1 Protein, Inflammation, Interleukin-1, Intra-Abdominal Fat, Leptin, Mesenchymal Stem Cells, Methionine, Mice, Obesity, Proteome, Proto-Oncogene Proteins C-Met, Receptor, Fibroblast Growth Factor, Type 2, Rna Precursors, Rna Processing, Post-Transcriptional, Secretory Vesicles, Signal Transduction, Transforming Growth Factor Beta, Vascular Endothelial Growth Factor Receptor-2, Wnt Signaling Pathway, Leptin, Aging, senescence, Proteome, Intra-Abdominal Fat, Diet, High-Fat, Granzymes, Mice, Methionine, RNA Precursors, Animals, Obesity, visceral adipose tissue, HMGB1 Protein, RNA Processing, Post-Transcriptional, Receptor, Fibroblast Growth Factor, Type 2, Inflammation, Secretory Vesicles, Mesenchymal Stem Cells, Proto-Oncogene Proteins c-met, mesenchymal stromal cells; senescence; visceral adipose tissue, mesenchymal stromal cells, Research Paper, Interleukin-1, Signal Transduction

Fields of Science

0301 basic medicine, 03 medical and health sciences

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12

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24

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24894

End Page

24913
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PubMed : 13

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