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Conditioned media from human palatine tonsil mesenchymal stem cells regulates the interaction between myotubes and fibroblasts by IL‐1Ra activity

Saturated free fatty acids (FFAs) act as lipid mediators and induce insulin resistance in skeletal muscle. Specifically, in obesity‐related diseases such as type 2 diabetes, FFAs directly reduce insulin sensitivity and glucose uptake in skeletal muscle. However, the knowledge of how FFAs mediate inf...

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Published in:Journal of cellular and molecular medicine 2017-01, Vol.21 (1), p.130-141
Main Authors: Cho, Kyung‐Ah, Park, Minhwa, Kim, Yu‐Hee, Woo, So‐Youn, Ryu, Kyung‐Ha
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description Saturated free fatty acids (FFAs) act as lipid mediators and induce insulin resistance in skeletal muscle. Specifically, in obesity‐related diseases such as type 2 diabetes, FFAs directly reduce insulin sensitivity and glucose uptake in skeletal muscle. However, the knowledge of how FFAs mediate inflammation and subsequent tissue disorders, including fibrosis in skeletal muscle, is limited. FFAs are a natural ligand for toll‐like receptor 2 (TLR2) and TLR4, and induce chronic low‐grade inflammation that directly stimulates skeletal muscle tissue. However, persistent inflammatory stimulation in tissues could induce pro‐fibrogenic processes that ultimately lead to perturbation of the tissue architecture and dysfunction. Therefore, blocking the link between inflammatory primed skeletal muscle tissue and connective tissue might be an efficient therapeutic option for treating obesity‐induced muscle inactivity. In this study, we investigated the impact of conditioned medium obtained from human palatine tonsil‐derived mesenchymal stem cells (T‐MSCs) on the interaction between skeletal muscle cells stimulated with palmitic acid (PA) and fibroblasts. We found that PA‐treated skeletal muscle cells actively secreted interleukin‐1β (IL‐1β) and augmented the migration, proliferation and expression of fibronectin in L929 fibroblasts. Furthermore, T‐CM inhibited the skeletal muscle cell‐derived pro‐fibrogenic effect via the production of the interleukin‐1 receptor antagonist (IL‐1Ra), which is an inhibitor of IL‐1 signalling. Taken together, our data provide novel insights into the therapeutic potential of T‐MSC‐mediated therapy for the treatment of pathophysiological processes that occur in skeletal muscle tissues under chronic inflammatory conditions.
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Specifically, in obesity‐related diseases such as type 2 diabetes, FFAs directly reduce insulin sensitivity and glucose uptake in skeletal muscle. However, the knowledge of how FFAs mediate inflammation and subsequent tissue disorders, including fibrosis in skeletal muscle, is limited. FFAs are a natural ligand for toll‐like receptor 2 (TLR2) and TLR4, and induce chronic low‐grade inflammation that directly stimulates skeletal muscle tissue. However, persistent inflammatory stimulation in tissues could induce pro‐fibrogenic processes that ultimately lead to perturbation of the tissue architecture and dysfunction. Therefore, blocking the link between inflammatory primed skeletal muscle tissue and connective tissue might be an efficient therapeutic option for treating obesity‐induced muscle inactivity. 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Taken together, our data provide novel insights into the therapeutic potential of T‐MSC‐mediated therapy for the treatment of pathophysiological processes that occur in skeletal muscle tissues under chronic inflammatory conditions.</description><identifier>ISSN: 1582-1838</identifier><identifier>EISSN: 1582-4934</identifier><identifier>DOI: 10.1111/jcmm.12947</identifier><identifier>PMID: 27619557</identifier><language>eng</language><publisher>England: John Wiley &amp; Sons, Inc</publisher><subject>Animals ; Arthritis ; Cell Line ; Cell proliferation ; Conditioning ; Connective tissues ; Culture Media, Conditioned - metabolism ; Diabetes mellitus ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 - metabolism ; fatty acid ; Fatty acids ; fibroblast ; Fibroblasts ; Fibroblasts - metabolism ; Fibronectin ; Fibrosis ; Genomes ; human palatine tonsil‐derived mesenchymal stem cells ; Humans ; IL‐1Ra ; IL‐1β ; Inflammation ; Insulin ; Insulin Resistance - physiology ; Interleukin 1 Receptor Antagonist Protein - metabolism ; Interleukin-1beta - metabolism ; Mesenchymal stem cells ; Mesenchymal Stromal Cells - metabolism ; Mesenchyme ; Mice ; Muscle Fibers, Skeletal - metabolism ; Muscle, Skeletal - metabolism ; Muscles ; Musculoskeletal system ; Myotubes ; Obesity ; Original ; Palatine Tonsil - metabolism ; Palmitic acid ; Skeletal muscle ; Stem cells ; Tissue engineering ; Tissues ; TLR2 protein ; TLR4 protein ; Toll-Like Receptor 2 - metabolism ; Toll-like receptors ; Tonsil</subject><ispartof>Journal of cellular and molecular medicine, 2017-01, Vol.21 (1), p.130-141</ispartof><rights>2016 The Authors. 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Specifically, in obesity‐related diseases such as type 2 diabetes, FFAs directly reduce insulin sensitivity and glucose uptake in skeletal muscle. However, the knowledge of how FFAs mediate inflammation and subsequent tissue disorders, including fibrosis in skeletal muscle, is limited. FFAs are a natural ligand for toll‐like receptor 2 (TLR2) and TLR4, and induce chronic low‐grade inflammation that directly stimulates skeletal muscle tissue. However, persistent inflammatory stimulation in tissues could induce pro‐fibrogenic processes that ultimately lead to perturbation of the tissue architecture and dysfunction. Therefore, blocking the link between inflammatory primed skeletal muscle tissue and connective tissue might be an efficient therapeutic option for treating obesity‐induced muscle inactivity. 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subjects Animals
Arthritis
Cell Line
Cell proliferation
Conditioning
Connective tissues
Culture Media, Conditioned - metabolism
Diabetes mellitus
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2 - metabolism
fatty acid
Fatty acids
fibroblast
Fibroblasts
Fibroblasts - metabolism
Fibronectin
Fibrosis
Genomes
human palatine tonsil‐derived mesenchymal stem cells
Humans
IL‐1Ra
IL‐1β
Inflammation
Insulin
Insulin Resistance - physiology
Interleukin 1 Receptor Antagonist Protein - metabolism
Interleukin-1beta - metabolism
Mesenchymal stem cells
Mesenchymal Stromal Cells - metabolism
Mesenchyme
Mice
Muscle Fibers, Skeletal - metabolism
Muscle, Skeletal - metabolism
Muscles
Musculoskeletal system
Myotubes
Obesity
Original
Palatine Tonsil - metabolism
Palmitic acid
Skeletal muscle
Stem cells
Tissue engineering
Tissues
TLR2 protein
TLR4 protein
Toll-Like Receptor 2 - metabolism
Toll-like receptors
Tonsil
title Conditioned media from human palatine tonsil mesenchymal stem cells regulates the interaction between myotubes and fibroblasts by IL‐1Ra activity
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