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TNF-Stimulated Gene-6 Is a Key Regulator in Switching Stemness and Biological Properties of Mesenchymal Stem Cells.
Romano, Barbara; Elangovan, Sudharshan; Erreni, Marco; Sala, Emanuela; Petti, Luciana; Kunderfranco, Paolo; Massimino, Luca; Restelli, Silvia; Sinha, Shruti; Lucchetti, Donatella; Anselmo, Achille; Colombo, Federico Simone; Stravalaci, Matteo; Arena, Vincenzo; D'Alessio, Silvia; Ungaro, Federica; Inforzato, Antonio; Izzo, Angelo A; Sgambato, Alessandro; Day, Anthony J; Vetrano, Stefania.
Afiliação
  • Romano B; Department of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
  • Elangovan S; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
  • Erreni M; IBD Center, Laboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center-IRCCS, Rozzano, Milan, Italy.
  • Sala E; Unit of Advanced Optical Microscopy, Humanitas Clinical and Research Center-IRCCS, Rozzano, Milan, Italy.
  • Petti L; IBD Center, Laboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center-IRCCS, Rozzano, Milan, Italy.
  • Kunderfranco P; IBD Center, Laboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center-IRCCS, Rozzano, Milan, Italy.
  • Massimino L; Bioinformatic Unit, Humanitas Clinical and Research Center-IRCCS, Rozzano, Milan, Italy.
  • Restelli S; Stem Cell and Neurogenesis Unit, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
  • Sinha S; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
  • Lucchetti D; IBD Center, Laboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center-IRCCS, Rozzano, Milan, Italy.
  • Anselmo A; Genome Biology Unit, Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" (INGM), Milan, Italy.
  • Colombo FS; Institute of General Pathology, Fondazione Policlinico Universitario Agostino Gemelli IRCCS-Catholic University, Rome, Italy.
  • Stravalaci M; Flow Cytometry Core, Humanitas Clinical and Research Center, Rozzano, Italy.
  • Arena V; Flow Cytometry Core, Humanitas Clinical and Research Center, Rozzano, Italy.
  • D'Alessio S; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
  • Ungaro F; Department of Immunology and Inflammation, Humanitas Clinical and Research Center-IRCCS, Rozzano, Milan, Italy.
  • Inforzato A; Area of Pathology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli-IRCCS.
  • Izzo AA; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
  • Sgambato A; IBD Center, Laboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center-IRCCS, Rozzano, Milan, Italy.
  • Day AJ; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
  • Vetrano S; IBD Center, Laboratory of Gastrointestinal Immunopathology, Humanitas Clinical and Research Center-IRCCS, Rozzano, Milan, Italy.
Stem Cells ; 37(7): 973-987, 2019 07.
Article em En | MEDLINE | ID: mdl-30942926
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Moléculas de Adesão Celular / Transformação Celular Neoplásica / Interleucina-6 / Células-Tronco Mesenquimais / Transcriptoma Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Moléculas de Adesão Celular / Transformação Celular Neoplásica / Interleucina-6 / Células-Tronco Mesenquimais / Transcriptoma Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article