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Mesoangioblasts at 20: From the embryonic aorta to the patient bed.
Cossu, Giulio; Tonlorenzi, Rossana; Brunelli, Silvia; Sampaolesi, Maurilio; Messina, Graziella; Azzoni, Emanuele; Benedetti, Sara; Biressi, Stefano; Bonfanti, Chiara; Bragg, Laricia; Camps, Jordi; Cappellari, Ornella; Cassano, Marco; Ciceri, Fabio; Coletta, Marcello; Covarello, Diego; Crippa, Stefania; Cusella-De Angelis, M Gabriella; De Angelis, Luciana; Dellavalle, Arianna; Diaz-Manera, Jordi; Galli, Daniela; Galli, Francesco; Gargioli, Cesare; Gerli, Mattia F M; Giacomazzi, Giorgia; Galvez, Beatriz G; Hoshiya, Hidetoshi; Guttinger, Maria; Innocenzi, Anna; Minasi, M Giulia; Perani, Laura; Previtali, Stefano C; Quattrocelli, Mattia; Ragazzi, Martina; Roostalu, Urmas; Rossi, Giuliana; Scardigli, Raffaella; Sirabella, Dario; Tedesco, Francesco Saverio; Torrente, Yvan; Ugarte, Gonzalo.
Afiliação
  • Cossu G; Division of Cell Matrix Biology and Regenerative Medicine. University of Manchester, Manchester, United Kingdom.
  • Tonlorenzi R; Division of Neuroscience, IRCCS Ospedale San Raffaele, Milan, Italy.
  • Brunelli S; Muscle Research Unit, Charité Medical Faculty and Max Delbrück Center, Berlin, Germany.
  • Sampaolesi M; Division of Neuroscience, IRCCS Ospedale San Raffaele, Milan, Italy.
  • Messina G; School of Medicine and Surgery, University of Milano Bicocca, Milan, Italy.
  • Azzoni E; Translational Cardiomyology Laboratory, Stem Cell and Developmental Biology Unit, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Benedetti S; Histology and Medical Embryology Unit, Department of Anatomy, Forensic Medicine and Orthopaedics, Sapienza University, Rome, Italy.
  • Biressi S; Department of Biosciences, University of Milan, Milan, Italy.
  • Bonfanti C; School of Medicine and Surgery, University of Milano Bicocca, Milan, Italy.
  • Bragg L; UCL Great Ormond Street Institute of Child Health and NIHR GOSH Biomedical Research Centre, London, United Kingdom.
  • Camps J; Department of Cellular, Computational and Integrative Biology (CIBIO) and Dulbecco Telethon Institute, University of Trento, Trento, Italy.
  • Cappellari O; Department of Biosciences, University of Milan, Milan, Italy.
  • Cassano M; Division of Cell Matrix Biology and Regenerative Medicine. University of Manchester, Manchester, United Kingdom.
  • Ciceri F; Bayer AG, Research and Development, Pharmaceuticals, Berlin, Germany.
  • Coletta M; Department of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Bari, Italy.
  • Covarello D; Lunaphore Technologies SA, Tolochenaz, Switzerland.
  • Crippa S; Division of Neuroscience, IRCCS Ospedale San Raffaele, Milan, Italy.
  • Cusella-De Angelis MG; Histology and Medical Embryology Unit, Department of Anatomy, Forensic Medicine and Orthopaedics, Sapienza University, Rome, Italy.
  • De Angelis L; AGC Biologicals, Milan, Italy.
  • Dellavalle A; San Raffaele-Telethon Institute of Gene Theray, IRCCS Ospedale San Raffaele, Milan, Italy.
  • Diaz-Manera J; Department of Anatomy, University of Pavia, Pavia, Italy.
  • Galli D; Histology and Medical Embryology Unit, Department of Anatomy, Forensic Medicine and Orthopaedics, Sapienza University, Rome, Italy.
  • Galli F; Cord Blood Bank, InScientiaFides, San Marino.
  • Gargioli C; John Walton Muscular Dystrophy Research Centre, Newcastle University, United Kingdom.
  • Gerli MFM; Department of Medicine and Surgery, University of Parma, Parma, Italy.
  • Giacomazzi G; Division of Cell Matrix Biology and Regenerative Medicine. University of Manchester, Manchester, United Kingdom.
  • Galvez BG; Department of Biology, University of Tor Vergata, Rome, Italy.
  • Hoshiya H; UCL Department of Surgical Biotechnology and Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Guttinger M; CellCarta, Gosselies, Belgium.
  • Innocenzi A; Department of Biochemistry and Molecular Biology, Faculty of Pharmacy, Universidad Complutense de Madrid, Madrid, Spain.
  • Minasi MG; CellFiber Co., Ltd, Tokyo, Japan.
  • Perani L; IFO, Istituti Fisioterapici Ospedalieri, Rome, Italy.
  • Previtali SC; Division of Neuroscience, IRCCS Ospedale San Raffaele, Milan, Italy.
  • Quattrocelli M; Lavitaminasi, Clinical Nutrition and Reproductive Medicine, Rome, Italy.
  • Ragazzi M; Division of Neuroscience, IRCCS Ospedale San Raffaele, Milan, Italy.
  • Roostalu U; Division of Neuroscience, IRCCS Ospedale San Raffaele, Milan, Italy.
  • Rossi G; Division of Molecular Cardiovascular Biology, University of Cincinnati, Cincinnati, OH, United States.
  • Scardigli R; Gubra ApS, Horsholm, Denmark.
  • Sirabella D; Roche Institute for Translational Bioengineering (ITB), pRED Basel, Basel, Switzerland.
  • Tedesco FS; Institute of Translational Pharmacology, National Research Council, Rome, Italy.
  • Torrente Y; Columbia Stem Cell Initiative, Department of Rehabilitation and Regenerative Medicine, Columbia University, New York, United States.
  • Ugarte G; University College London, Great Ormond Street Hospital for Children and the Francis Crick Institute, London, United Kingdom.
Front Genet ; 13: 1056114, 2022.
Article em En | MEDLINE | ID: mdl-36685855
In 2002 we published an article describing a population of vessel-associated progenitors that we termed mesoangioblasts (MABs). During the past decade evidence had accumulated that during muscle development and regeneration things may be more complex than a simple sequence of binary choices (e.g., dorsal vs. ventral somite). LacZ expressing fibroblasts could fuse with unlabelled myoblasts but not among themselves or with other cell types. Bone marrow derived, circulating progenitors were able to participate in muscle regeneration, though in very small percentage. Searching for the embryonic origin of these progenitors, we identified them as originating at least in part from the embryonic aorta and, at later stages, from the microvasculature of skeletal muscle. While continuing to investigate origin and fate of MABs, the fact that they could be expanded in vitro (also from human muscle) and cross the vessel wall, suggested a protocol for the cell therapy of muscular dystrophies. We tested this protocol in mice and dogs before proceeding to the first clinical trial on Duchenne Muscular Dystrophy patients that showed safety but minimal efficacy. In the last years, we have worked to overcome the problem of low engraftment and tried to understand their role as auxiliary myogenic progenitors during development and regeneration.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article