Mécanismes cellulaires et moléculaires des désordres hématologiques et implications thérapeutiques
Publié le 18.11.2019
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The laboratory of Hematology of Imagine Institute covers several aspects of the physiopathology and treatment of malignant and benign hematologic disorders. The Department belongs to INSERM U 1163 research units and is associated to the Necker Hospital clinical hematological department of hematology as well as to national reference centers for mastocytosis (CEREMAST), immunodeficiencies (CEREDIH) and hemoglobinopathies. Our group has as major objectives: i- the characterization of mechanisms governing the physiopathology of hematological disorders; ii- the development of therapeutic strategies to treat these diseases; iii- the development of clinical research and iv- technology transfer. We work in close collaboration with the Necker pathology, biology, cytogenetics, molecular biology, biotherapy, infectious disease, transplantation and pediatric immune hematology departments.
Erythropoiesis regulation and its clinical applications
Our research group has been working from the last years in erythropoiesis and erythropoietic disorders. We were particularly interested in the molecular mechanisms involved in the positive and negative regulation of erythropoiesis and how alterations in this system impacts in hematopoietic disorders. We have shown that caspases activation is critical for erythroid differentiation. Our current aims are: (i) to decipher the mechanisms triggering caspase activation; (ii) to identify parameters that control caspase activity, the downstream caspase targets; (iii) to characterize the involvement of caspases and protrins that regulates their functions, particularly HSP70, in the physiopathology of erythroid disorders such as thalassemia, myelodysplastic syndrome (MDS) and congenital erythroblastopenia; (iv) to determine the potential therapeutic application of caspases targeting in erythropoiesis disorders.
In Thalassemia we have identified that member of the TGF-beta family are key regulators of ineffective erythropoiesis of thalassemia. We are currently deciphering the molecular and cellular mechanisms involved with these cytokines in the induction of ineffective eryhtropoiesis, developing therapeutic strategies by using inhibitors and extending our findingsin several hematological disorders. We have shown that transferrin receptor (TfR1) is a signaling competent molecule able to regulate erythropoiesis independently of its essential role in iron transport. We are currently characterizing the molecular pathways involved in this process. We have developed TfR1 mutants in the intracytoplasmic tail of the receptor that will be used to identify molecular partners, which could be involved in the first steps of cell activation. Our goal is to identify the role of such molecular pathways in erythropoiesis as well as in other hematological disorders.
TfR1 is overexpressed in cancer cells compared to their non-malignant counterparts and several studies have suggested the therapeutic potential of targeting this receptor in cancer. We are currently developing, in collaboration with the startup Inatherys (Ivan Moura and Olivier Hermine co-founders) an antibody directed against TfR1 to treat malignant diseases.
Recently we developed a new field of research on the role of serotonin in erythropoiesis and red blood cells survival. To define the in vivo action of serotonin (5-hydroxytryptamine, 5-HT) we generated mice with a deletion of the gene encoding tryptophan hydroxylase-1 (Tph1). Our findings revealed that 5-HT is of pivotal importance to normal erythropoiesis and red blood cell (RBC) survival in mice. We will investigate mechanisms of 5-HT regulation and mechanisms of action of serotonin on erythroid differentiation, survival and proliferation as well as in iron metabolism. We will particularly give attention in the study of protein serotonylation, the modulation of ROS responses and the production of members of the TGF-beta; family. We will also investigate whether serotonin expression plays a role in erythroid disorders including thalassemia, MDS and primary myelofibrosis (MF) since our preliminary data suggest that old Tph1-/- mice develop MF. This work might be the basis of new therapeutic tools in erythroid disorders. In parallel we are currently investigating the role of serotonin in red blood cell preservation for blood transfusion.
Red blood cell transfusion is widely used in the management of different disorders. However its impact on the outcome of such diseases is poorly known. We are currently studying the role of red blood cells transfusions in cancer and immune diseases progression.
Mastocytosis and role of mast cells in disease
Mastocytosis is a rare disease caused by the accumulation of mast cells in various tissues. The pediatric form of mastocytosis is a clonal disease associated with mutations of the C-Kit gene and may resolve spontaneously. C-Kit mutations differed between adults and pediatric patients suggesting that different mutations could dictate the outcome of the disease. We are currently trying to understand how these mutations may explain the phenotype and the disease outcome and how they can be targeted to treat what is still an incurable disease in adult patients.
Mastocytosis is a frequent disease in dogs. We have identified canine C-kit mutations and shown that they are similar to those found in pediatric diseases. In collaboration with a pharmaceutical company (AB Science, Oliver Hermine co-founder) we have demonstrated that kinase inhibitors that block KIT may reduce mast cell infiltration and the symptoms associated with mast cells mediators release in dogs. Clinical trials are now running in humans mastocytosis by using kinase inhibitors.
Mast cells may play a critical role in various inflammatory, neurological and neoplastic diseases, and that these diseases can be targeted by kinase inhibitors targeting mast cells. We will use as a model naturally occurring neoplastic and inflammatory diseases in dogs to test this hypothesis.
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La recherche : une aventure scientifique
Notre objectif : mieux comprendre les maladies génétiques pour mieux les soigner.