TROLLET/MOULY Lab

Cellular and molecular orchestration in muscle regeneration, during ageing and in pathologies.

The team focuses on molecular and cellular actors involved in human in skeletal muscle regeneration, during ageing and in muscle dystrophies, particularly oculo-pharyngeal muscular dystrophy (OPMD) and Duchenne muscular dystrophy (DMD). Our approaches aim at better understandng RNA metabolism, muscle regeneration, muscle stem cells and fibrosis, in order to develop therapeutic strategies.The team has developed a solid expertise on cellular models (incuding through the MyoLine platform for immortalization taht we have set up) and on xenotransplantation using several immunodeficient mouse models and different types of grafts.

Research projects currently developed in parralel and in synergy within the team :

  • Molecular mechanisms involved in OPMD and in muscle ageing
  • Cell-to-cell communication during muscle regeneration, muscle ageing and fibrosis
  • Development of therapeutic strategies

 

International associated laboratory (LIA) between France and Brazil:

Another aspect specific to our team is the development of international collaborations. In addition to numerous collaborations established over many years, we have set up an international associated laboratory between INSERM and Sorbonne University on the French side, and FIOCRUZ and the Federal University of Rio-de-Janeiro for the brazilian side. This LIA aims at synergize expertises on skeletal muscle and neuromuscular diseases from the French team and on inflammation from the Brazilian team. This LIA has been renew already once, and has produced 14 common publications, a common patent, long-term exchanges of 3 post-docs, 5 common PhD and many short term exchanges, including invited professors in both countries. A common teaching project is being set up (master and/or PhD), which will focus on innovative biotherapies for skeletal muscle.

Capucine Trollet et Vincent Mouly

Capucine Trollet et Vincent Mouly

NamePositionEmailORCID



216 documents

  • Eunhye Kim, Fang Wu, Danbi Lim, Christopher Zeuthen, Yiming Zhang, et al.. Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion. Frontiers in Cell and Developmental Biology, 2022, 10, ⟨10.3389/fcell.2022.875209⟩. ⟨hal-03820132⟩
  • Laura Le Gall, William Duddy, Cecile Martinat, Virginie Mariot, Owen Connolly, et al.. Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles. Journal of Cachexia, Sarcopenia and Muscle, 2022, 13 (2), pp.1385-1402. ⟨10.1002/jcsm.12945⟩. ⟨hal-04293376⟩
  • Ingo Riederer, Daniella Arêas Mendes-Da-Cruz, Guilherme Cordenonsi da Fonseca, Mariela Natacha González, Otavio Brustolini, et al.. Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection. PLoS Neglected Tropical Diseases, 2022, 16 (2), pp.e0010166. ⟨10.1371/journal.pntd.0010166⟩. ⟨hal-03832616⟩
  • Alexis Boulinguiez, Fanny Roth, Jamila Dhiab, Hadidja Rose Mouigni, Saskia Lassche, et al.. Status and role of PABPN1 nuclear aggregates in Oculopharyngeal Muscular Dystrophy. 19èmes Journées de la Société Française de Myologie, 2022, Toulouse, France. ⟨hal-04011442⟩
  • Hadidja-Rose Mouigni, Nami Altin, Jamila Dhiab, Fanny Roth, Jean Lacau-St Guily, et al.. Control of PABPN1 expression in skeletal muscle. 19èmes Journées de la Société Française de Myologie, 2022, Toulouse, France. ⟨hal-04010992⟩
  • Laura Muraine, Mona Bensalah, Jamila Dhiab, Stephen Gargan, Paul Dowling, et al.. Molecular and cellular actors of human muscle fibrosis among different muscular disorders. Journées Boris Ephrussi, 2022, Paris, France. ⟨hal-04011029⟩
  • M Bensalah, L Muraine, A Boulinguiez, Lorenzo Giordani, V Albert, et al.. A negative feedback loop between fibroadipogenic progenitors and muscle fibres involving endothelin promotes human muscle fibrosis.. Journal of Cachexia, Sarcopenia and Muscle, In press, ⟨10.1002/jcsm.12974⟩. ⟨hal-03618341⟩
  • Hadidja-Rose Mouigni, Nami Altin, Jamila Dhiab, Fanny Roth, Jean Lacau-St Guily, et al.. Control of PABPN1 expression in human skeletal muscle. Post-transcriptional Control of Gene Expression Conference: Mechanisms of RNA Decay, 2022, Jupiter, United States. ⟨hal-04011417⟩
  • Mona Bensalah. Muscle fibrosis: a vicious circle between human fibroadipogenic progenitors and muscle fibers. Colloque Reseau 'Cellules Souches et Medecine Regeneratrice', 2022, Paris, France. ⟨hal-04011445⟩
  • Negroni Elisa. Cellular and moleculars actors of human muscular fibrosis in muscular disorders. 19èmes Journées de la Société Française de Myologie, 2022, Toulouse, France. ⟨hal-04011428⟩
AFM Telethon : innover pour guérir
Assistance Publique Hôpitaux de Paris
FRM - Fondation Recherche Médicale
ERA-Net for Research Programmes on Rare Diseases
Coordinating research in the area of nutrition,  diet, health and physical activity
Fondation de l'avenir - Accélérateur de progrès médical
Université Sorbonne Paris Nord
Fondation Maladies Rares - Ensemble, trouvons des traitements !

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