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Lipid availability determines fate of skeletal progenitor cells via SOX9.
van Gastel, Nick; Stegen, Steve; Eelen, Guy; Schoors, Sandra; Carlier, Aurélie; Daniëls, Veerle W; Baryawno, Ninib; Przybylski, Dariusz; Depypere, Maarten; Stiers, Pieter-Jan; Lambrechts, Dennis; Van Looveren, Riet; Torrekens, Sophie; Sharda, Azeem; Agostinis, Patrizia; Lambrechts, Diether; Maes, Frederik; Swinnen, Johan V; Geris, Liesbet; Van Oosterwyck, Hans; Thienpont, Bernard; Carmeliet, Peter; Scadden, David T; Carmeliet, Geert.
Afiliação
  • van Gastel N; Laboratory of Clinical and Experimental Endocrinology, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, Belgium.
  • Stegen S; Prometheus, Division of Skeletal Tissue Engineering, KU Leuven, Leuven, Belgium.
  • Eelen G; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Schoors S; Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
  • Carlier A; Center for Regenerative Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Daniëls VW; Laboratory of Clinical and Experimental Endocrinology, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, Belgium.
  • Baryawno N; Prometheus, Division of Skeletal Tissue Engineering, KU Leuven, Leuven, Belgium.
  • Przybylski D; Laboratory of Angiogenesis and Vascular Metabolism, Department of Oncology, KU Leuven, Leuven, Belgium.
  • Depypere M; Laboratory of Angiogenesis and Vascular Metabolism, Center for Cancer Biology, VIB, Leuven, Belgium.
  • Stiers PJ; Laboratory of Angiogenesis and Vascular Metabolism, Department of Oncology, KU Leuven, Leuven, Belgium.
  • Lambrechts D; Laboratory of Angiogenesis and Vascular Metabolism, Center for Cancer Biology, VIB, Leuven, Belgium.
  • Van Looveren R; Prometheus, Division of Skeletal Tissue Engineering, KU Leuven, Leuven, Belgium.
  • Torrekens S; Biomechanics Section, Department of Mechanical Engineering, KU Leuven, Leuven, Belgium.
  • Sharda A; Biomechanics Research Unit, GIGA In Silico Medicine, University of Liège, Liège, Belgium.
  • Agostinis P; MERLN Institute of Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
  • Lambrechts D; Laboratory of Lipid Metabolism and Cancer, Department of Oncology, KU Leuven, Leuven, Belgium.
  • Maes F; Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
  • Swinnen JV; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Geris L; Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
  • Van Oosterwyck H; Center for Regenerative Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Thienpont B; Childhood Cancer Research Unit, Department of Children's and Women's Health, Karolinska Institutet, Stockholm, Sweden.
  • Carmeliet P; Howard Hughes Medical Institute and Department of Biology, Brandeis University, Waltham, MA, USA.
  • Scadden DT; Medical Imaging Research Center, KU Leuven, Leuven, Belgium.
  • Carmeliet G; Department of Electrical Engineering, ESAT/PSI, Medical Image Computing, KU Leuven, Leuven, Belgium.
Nature ; 579(7797): 111-117, 2020 03.
Article em En | MEDLINE | ID: mdl-32103177
The avascular nature of cartilage makes it a unique tissue1-4, but whether and how the absence of nutrient supply regulates chondrogenesis remain unknown. Here we show that obstruction of vascular invasion during bone healing favours chondrogenic over osteogenic differentiation of skeletal progenitor cells. Unexpectedly, this process is driven by a decreased availability of extracellular lipids. When lipids are scarce, skeletal progenitors activate forkhead box O (FOXO) transcription factors, which bind to the Sox9 promoter and increase its expression. Besides initiating chondrogenesis, SOX9 acts as a regulator of cellular metabolism by suppressing oxidation of fatty acids, and thus adapts the cells to an avascular life. Our results define lipid scarcity as an important determinant of chondrogenic commitment, reveal a role for FOXO transcription factors during lipid starvation, and identify SOX9 as a critical metabolic mediator. These data highlight the importance of the nutritional microenvironment in the specification of skeletal cell fate.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco / Osso e Ossos / Condrogênese / Metabolismo dos Lipídeos / Fatores de Transcrição SOX9 / Microambiente Celular Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco / Osso e Ossos / Condrogênese / Metabolismo dos Lipídeos / Fatores de Transcrição SOX9 / Microambiente Celular Idioma: En Ano de publicação: 2020 Tipo de documento: Article