TY - JOUR
T1 - TNF-Stimulated Gene-6 Is a Key Regulator in Switching Stemness and Biological Properties of Mesenchymal Stem Cells
AU - Romano, Barbara
AU - Romano, Benedetta
AU - Elangovan, Sudharshan
AU - Erreni, Marco
AU - Sala, Emanuela
AU - Sala, Elisabetta
AU - Petti, Luciana
AU - Petti, Livia
AU - Kunderfranco, Paolo
AU - Massimino, Luca
AU - Restelli, Silvia
AU - Sinha, Shruti
AU - Lucchetti, Donatella
AU - Anselmo, Achille
AU - Anselmo, Anna
AU - Colombo, Federico Simone
AU - Stravalaci, Matteo
AU - Arena, Vincenzo
AU - D'Alessio, Silvia
AU - Ungaro, Federica
AU - Ungaro, Francesco
AU - Inforzato, Antonio
AU - Izzo, Angelo A.
AU - Sgambato, Alessandro
AU - Day, Anthony J.
AU - Vetrano, Stefania
PY - 2019
Y1 - 2019
N2 - Mesenchymal stem cells (MSCs) are well established to have promising therapeutic properties. TNF-stimulated gene-6 (TSG-6), a potent tissue-protective and anti-inflammatory factor, has been demonstrated to be responsible for a significant part of the tissue-protecting properties mediated by MSCs. Nevertheless, current knowledge about the biological function of TSG-6 in MSCs is limited. Here, we demonstrated that TSG-6 is a crucial factor that influences many functional properties of MSCs. The transcriptomic sequencing analysis of wild-type (WT) and TSG-6−/−-MSCs shows that the loss of TSG-6 expression leads to the perturbation of several transcription factors, cytokines, and other key biological pathways. TSG-6−/−-MSCs appeared morphologically different with dissimilar cytoskeleton organization, significantly reduced size of extracellular vesicles, decreased cell proliferative rate, and loss of differentiation abilities compared with the WT cells. These cellular effects may be due to TSG-6-mediated changes in the extracellular matrix (ECM) environment. The supplementation of ECM with exogenous TSG-6, in fact, rescued cell proliferation and changes in morphology. Importantly, TSG-6-deficient MSCs displayed an increased capacity to release interleukin-6 conferring pro-inflammatory and pro-tumorigenic properties to the MSCs. Overall, our data provide strong evidence that TSG-6 is crucial for the maintenance of stemness and other biological properties of murine MSCs.
AB - Mesenchymal stem cells (MSCs) are well established to have promising therapeutic properties. TNF-stimulated gene-6 (TSG-6), a potent tissue-protective and anti-inflammatory factor, has been demonstrated to be responsible for a significant part of the tissue-protecting properties mediated by MSCs. Nevertheless, current knowledge about the biological function of TSG-6 in MSCs is limited. Here, we demonstrated that TSG-6 is a crucial factor that influences many functional properties of MSCs. The transcriptomic sequencing analysis of wild-type (WT) and TSG-6−/−-MSCs shows that the loss of TSG-6 expression leads to the perturbation of several transcription factors, cytokines, and other key biological pathways. TSG-6−/−-MSCs appeared morphologically different with dissimilar cytoskeleton organization, significantly reduced size of extracellular vesicles, decreased cell proliferative rate, and loss of differentiation abilities compared with the WT cells. These cellular effects may be due to TSG-6-mediated changes in the extracellular matrix (ECM) environment. The supplementation of ECM with exogenous TSG-6, in fact, rescued cell proliferation and changes in morphology. Importantly, TSG-6-deficient MSCs displayed an increased capacity to release interleukin-6 conferring pro-inflammatory and pro-tumorigenic properties to the MSCs. Overall, our data provide strong evidence that TSG-6 is crucial for the maintenance of stemness and other biological properties of murine MSCs.
KW - Animals
KW - Autocrine Communication
KW - Cell Adhesion Molecules
KW - Cell Proliferation
KW - Cell Transformation, Neoplastic
KW - Cytokines
KW - Cytoskeleton
KW - Extracellular Matrix
KW - Extracellular Vesicles
KW - Female
KW - Gene Expression Profiling
KW - Humans
KW - Interleukin-6
KW - Male
KW - Mesenchymal Stem Cells
KW - Metabolic Networks and Pathways
KW - Mice
KW - Mice, Inbred BALB C
KW - Mice, Knockout
KW - Transcription Factors
KW - Transcriptome
KW - Animals
KW - Autocrine Communication
KW - Cell Adhesion Molecules
KW - Cell Proliferation
KW - Cell Transformation, Neoplastic
KW - Cytokines
KW - Cytoskeleton
KW - Extracellular Matrix
KW - Extracellular Vesicles
KW - Female
KW - Gene Expression Profiling
KW - Humans
KW - Interleukin-6
KW - Male
KW - Mesenchymal Stem Cells
KW - Metabolic Networks and Pathways
KW - Mice
KW - Mice, Inbred BALB C
KW - Mice, Knockout
KW - Transcription Factors
KW - Transcriptome
UR - http://hdl.handle.net/10807/170793
U2 - 10.1002/stem.3010
DO - 10.1002/stem.3010
M3 - Article
SN - 1066-5099
VL - 37
SP - 973
EP - 987
JO - Stem Cells
JF - Stem Cells
ER -