An adult tissue-specific stem cell in its niche: A gene profiling analysis of in vivo quiescent and activated muscle satellite cells

Autor: Didier Montarras, Stéphanie François, Ana Cumano, Bertrand Czarny, Giorgia Pallafacchina, Béatrice Regnault, Vincent Dive, Margaret Buckingham
Přispěvatelé: Génétique Moléculaire du Développement, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Génopole, Institut Pasteur [Paris] (IP), Département d'Ingénierie et Etudes des Protéines, Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Développement des Lymphocytes, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Institut Pasteur [Paris], Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)
Jazyk: angličtina
Rok vydání: 2010
Předmět:
MESH: Signal Transduction
Cell
Fluorescent Antibody Technique
MESH: Flow Cytometry
Polymerase Chain Reaction
Extracellular matrix
Transcriptome
Mice
0302 clinical medicine
MESH: Eye Proteins
MESH: Gene Expression Regulation
Developmental

MESH: Animals
MESH: Fluorescent Antibody Technique
Cells
Cultured

Oligonucleotide Array Sequence Analysis
Medicine(all)
0303 health sciences
Stem Cells
MESH: Satellite Cells
Skeletal Muscle

Gene Expression Regulation
Developmental

General Medicine
Flow Cytometry
Cell biology
medicine.anatomical_structure
[SDV.IMM]Life Sciences [q-bio]/Immunology
Stem cell
Cell activation
Signal Transduction
MESH: Cells
Cultured

Satellite Cells
Skeletal Muscle

MESH: Mice
Transgenic

Blotting
Western

Mice
Transgenic

MESH: Stem Cells
Biology
03 medical and health sciences
MESH: Gene Expression Profiling
MESH: Cell Proliferation
medicine
Animals
MESH: Blotting
Western

Eye Proteins
Cell adhesion
MESH: Mice
Cell Proliferation
030304 developmental biology
Gene Expression Profiling
Skeletal muscle
MESH: Polymerase Chain Reaction
Cell Biology
Cell culture
MESH: Oligonucleotide Array Sequence Analysis
030217 neurology & neurosurgery
Developmental Biology
Zdroj: Stem Cell Research
Stem Cell Research; Vol 4
Stem Cell Research, 2010, 4 (2), pp.77-91. ⟨10.1016/j.scr.2009.10.003⟩
Stem Cell Research, Elsevier, 2010, 4 (2), pp.77-91. ⟨10.1016/j.scr.2009.10.003⟩
ISSN: 1873-5061
1876-7753
DOI: 10.1016/j.scr.2009.10.003
Popis: International audience; The satellite cell of skeletal muscle provides a paradigm for quiescent and activated tissue stem cell states. We have carried out transcriptome analyses on satellite cells purified by flow cytometry from Pax3(GFP/+) mice. We compared samples from adult skeletal muscles where satellite cells are mainly quiescent, with samples from growing muscles or regenerating (mdx) muscles, where they are activated. Analysis of regulation that is shared by both activated states avoids other effects due to immature or pathological conditions. This in vivo profile differs from that of previously analyzed satellite cells activated after cell culture. It reveals how the satellite cell protects itself from damage and maintains quiescence, while being primed for activation on receipt of the appropriate signal. This is illustrated by manipulation of the corepressor Dach1, and by the demonstration that quiescent satellite cells are better protected from oxidative stress than those from mdx or 1-week-old muscles. The quiescent versus in vivo activated comparison also gives new insights into how the satellite cell controls its niche on the muscle fiber through cell adhesion and matrix remodeling. The latter also potentiates growth factor activity through proteoglycan modification. Dismantling the extracellular matrix is important for satellite cell activation when the expression of proteinases is up-regulated, whereas transcripts for their inhibitors are high in quiescent cells. In keeping with this, we demonstrate that metalloproteinase function is required for efficient regeneration in vivo.
Databáze: OpenAIRE